Logo of bmcmedicineBioMed Centralsearchsubmit a manuscriptregisterthis articleBMC Medicine
BMC Med. 2009; 7: 36.
Published online 2009 Jul 29. doi:  10.1186/1741-7015-7-36
PMCID: PMC2744672

Systematic review of the relation between smokeless tobacco and cancer in Europe and North America



Interest is rising in smokeless tobacco as a safer alternative to smoking, but published reviews on smokeless tobacco and cancer are limited. We review North American and European studies and compare effects of smokeless tobacco and smoking.


We obtained papers from MEDLINE searches, published reviews and secondary references describing epidemiological cohort and case-control studies relating any form of cancer to smokeless tobacco use. For each study, details were abstracted on design, smokeless tobacco exposure, cancers studied, analysis methods and adjustment for smoking and other factors. For each cancer, relative risks or odds ratios with 95% confidence intervals were tabulated. Overall, and also for USA and Scandinavia separately, meta-analyses were conducted using all available estimates, smoking-adjusted estimates, or estimates for never smokers. For seven cancers, smoking-attributable deaths in US men in 2005 were compared with deaths attributable to introducing smokeless tobacco into a population of never-smoking men.


Eighty-nine studies were identified; 62 US and 18 Scandinavian. Forty-six (52%) controlled for smoking. Random-effects meta-analysis estimates for most sites showed little association. Smoking-adjusted estimates were only significant for oropharyngeal cancer (1.36, CI 1.04–1.77, n = 19) and prostate cancer (1.29, 1.07–1.55, n = 4). The oropharyngeal association disappeared for estimates published since 1990 (1.00, 0.83–1.20, n = 14), for Scandinavia (0.97, 0.68–1.37, n = 7), and for alcohol-adjusted estimates (1.07, 0.84–1.37, n = 10). Any effect of current US products or Scandinavian snuff seems very limited. The prostate cancer data are inadequate for a clear conclusion.

Some meta-analyses suggest a possible effect for oesophagus, pancreas, larynx and kidney cancer, but other cancers show no effect of smokeless tobacco. Any possible effects are not evident in Scandinavia. Of 142,205 smoking-related male US cancer deaths in 2005, 104,737 are smoking-attributable. Smokeless tobacco-attributable deaths would be 1,102 (1.1%) if as many used smokeless tobacco as had smoked, and 2,081 (2.0%) if everyone used smokeless tobacco.


An increased risk of oropharyngeal cancer is evident most clearly for past smokeless tobacco use in the USA, but not for Scandinavian snuff. Effects of smokeless tobacco use on other cancers are not clearly demonstrated. Risk from modern products is much less than for smoking.


Over the last 10 years, interest in smokeless tobacco (ST) as a possible safer alternative to smoking has risen. Although a number of recent reviews have considered the evidence relating ST to cancer, some have not included meta-analyses [1-3], and others have only provided quantitative summaries for specific sites: oropharyngeal cancer [4], pancreatic cancer [5], or oropharyngeal, oesophageal, pancreatic and lung cancer [6]. No formal comparisons have been conducted with the well-known effects of smoking [7,8].

The review described in this paper is restricted to studies in Western populations. In practice this predominantly means studies in the USA and Sweden, the only North American and European countries where the two major types of ST – chewing tobacco and snuff – are commonly used [2]. Although ST is also widely used in developing countries, particularly parts of Central and South-East Asia, the tobacco is often used in combination with other products, such as betel nut quid, slaked lime, areca nut and even snail shells [1,2,9]. This review also does not consider the limited data on nicotine chewing gum.

Our first objective is to carry out a comprehensive review of the available epidemiological evidence in Western countries relating ST to cancer, including meta-analyses for as many cancer types as the data justify. In meeting this objective, we take proper account of the potential confounding role of smoking by distinguishing effect estimates which are unadjusted for smoking and those which take smoking into account (either by adjustment in analyses based on the whole population of smokers and non-smokers combined or by restricting analysis to lifelong never smokers). Our second objective is to provide a quantitative indication of the relative effects of ST and cigarette smoking.


Study identification and selection

All reports had to satisfy the following inclusion criteria: published in a peer reviewed journal or the results publicly available, epidemiological study in humans, of cohort or case-control design, study location specified, any form of cancer as the outcome, and chewing tobacco, oral snuff or unspecified ST as the exposure. They also had to fall outside the exclusion criteria: conducted in an Asian or African population, no control group, or inappropriate design (case report, qualitative study or review/meta-analysis). Relevant papers were sought from a MEDLINE search conducted in May 2008 of "cancer" AND ("smokeless tobacco" OR "chewing tobacco" OR "snuff" OR "snus"), supplemented by citations in recent reviews [1-6,10] and in the papers obtained.

Data extraction

Reports were grouped by study, and for each study details were abstracted (see Tables Tables11 and and22[11-114]) relating to the design, period, location, controls used and size, the exposure (method of assessment, type of ST, exposure doses and durations considered), the outcome (cancer sites studied) and issues relating to analysis (type of effect measure, analysis methods, extent of adjustment for smoking and other factors, and availability of dose-response data). The extent of adjustment for smoking for a study was categorised into five groups: A. no information – effect estimates are provided but no details are given of any adjustments made; B. no adjustment – effect estimates are available for the whole population, but smoking is not taken into account; C. never smokers – the only effect estimates available are for never smokers; D. some adjustment – effect estimates adjusted for smoking are available, but the adjustment is relatively simple, using two or three level broad groupings (for example, ever/never smoked, current/non-current smoker, current/former/never smoker), and takes no account of daily amount smoked or duration of smoking; and E. more adjustment – effect estimates are available that take into account daily amount smoked, duration of smoking and/or their product (pack-years). Studies were categorised under D or E if smoking-adjusted effect estimates are available, regardless of whether some results for never smokers are also presented. The method used to adjust for smoking is not always clear. Studies where the authors merely report that they 'adjusted for cigarette smoking' are included in category D.

Table 1
Cohort studies of smokeless tobacco and cancer
Table 2
Case-control studies of smokeless tobacco and cancer

Based on the availability of relevant data, 13 cancer groupings (oropharyngeal, oesophagus, stomach, pancreas, other digestive, larynx and nasal, lung, prostate, bladder, kidney, haematopoietic and lymphoid, other and all), were selected, with results for each grouping tabulated in a standard way, with details given of the source, exposure to ST, smoking group, sex, number of cases and adjustment factors for each effect estimate or indication of association (see tables dealing with individual effects estimates, below). For each study the intent is to extract the relative risk (RR) or odds ratio (OR) adjusted for the most factors, relevant to current, former or ever exposure to chewing tobacco, snuff or overall/undefined ST. Where relevant results for a study are reported in more than one paper, those based on the greatest number of cases are used.

Results are included, where available, for the whole population and for never smokers, and for sexes separately. RR or OR estimates based on zero exposed cases (or controls) are not included as providing too little information and because a valid confidence interval (CI) cannot be calculated. Suitable estimates of effect (RR or OR) and precision (CI) provided by the authors are used if possible, estimates otherwise being calculated from available data presented in the source publication, based on methods [115-118] summarised elsewhere [4]. Where an effect estimate cannot be calculated, statements made by the authors are summarised into terms such as 'no association' or 'no significant association'. Data are summarised for all types of cancer, except those relating to subdivision by type within site (for example, adenocarcinoma or squamous cell carcinoma of the lung, or t(14; 18)-positive and -negative non-Hodgkin's lymphoma or those relating to combined 'other' groups of cancers, which typically vary in definition from study to study).

Data presentation

Study-specific results for the different types of cancer are presented in an essentially identical format, with a standard set of information included for each effect estimate included. Points to note about the entries in the various columns are discussed below.


For the case-control studies, the source reference is shown. For the cohort studies, the source reference is also shown, but the study is also identified by name.

ST use – type

The exposure is identified as chewing tobacco ('chew'), 'snuff' or smokeless tobacco ('ST'). ST implies the results relate to smokeless tobacco unspecified by the author, or to use of either chewing tobacco or snuff or both.

ST use – exposure

Results are presented for current, former or ever use, or simply for 'use' where the timing of exposure was unspecified by the author. For current, former or ever use, the comparison is with never use; for use, it is with non-use.


Results are presented only for any smoking (that is, based on the combined population of ever and never smokers) and for never smokers.


Results are shown, where available, for the sexes separately, though in some studies results are given only for the sexes combined.

RR/OR id

Within each table, each effect estimate (RR or OR) is given a unique identification number, so that those which are included in specific meta-analyses can readily be seen.


The number of ST-exposed cases is shown. Total numbers of cases are given elsewhere. Estimates are not presented unless there is at least one exposed case.

Estimate (95% CI)

This is the RR for cohort studies or the OR for case-control studies, together with its 95% CI. For many studies, the estimates are not given directly in the source paper, but were calculated from data provided. This involved one or more of the following: estimating numbers of exposed and unexposed cases and controls from proportions exposed given numerically or graphically and, where appropriate, combining numbers over level of exposure or cancer subtype; calculating estimates from a 2 × 2 table, or multiple independent 2 × 2 tables using standard methods [115], and calculating estimates from non-independent RR/ORs by level of exposure or by cancer type using the method of Hamling et al. 2007 [118]. Fuller details of the method of calculation used for each estimate are available on request. In a limited number of studies, as indicated in the tables, estimates were available separately for chewing tobacco and for snuff, but data were lacking for joint use. Here estimates for combined ST use were calculated assuming that no one used both chewing tobacco and snuff. Where there is a choice of relevant estimates from a study, preference is given to the estimate adjusted for the most potential confounding factors, and, for cohort studies, the estimate from the publication with a longer follow-up period.

Adjustment factors

The adjustment factors used for each estimate are shown. For matched case-control studies, the matching factors are not included unless the estimate specifically took this into account (for example, by conditional logistic regression). The factors used have been simplified into a relatively short consistent list, rather than repeating verbatim the wide variety of variable descriptions given by the original authors. Thus 'res' (area of residence) includes any variable based on the location of the subject and, for example, includes centre in multicentre case-control studies. 'Diet' includes any aspect of diet, and 'alc' (alcohol) any aspect of alcohol use. Estimates relevant to never smokers are not listed as being adjusted for smoking ('smok').


For the five columns, ST use – type, ST use – exposure, smoking, sex and adjustment factors, any blank entry for a particular effect estimate is assumed to be the same as in the first previous non-blank entry in that column. This avoids needless repetition and makes the tables easier to read.


Estimates with no CI are not included in the meta-analyses. The standard error of the logarithm of estimates of effect size was calculated from its reported or estimated CI, assuming that the effect size was log-normally distributed. The logarithms of the effect sizes and their corresponding standard errors form the data points for fixed-effect and random-effects meta-analysis [116].

For most cancer groupings, results of nine random-effect meta-analyses are presented, subject to availability of data (see tables summarising meta-analysis results, below). In the first set of three, any, there is no restriction of estimates on type of exposure or region. In the second set, any ST use (USA), estimates are restricted to those from studies conducted in the USA (or on occasion in Puerto Rico), while in the third set, snuff (Scandinavia), estimates are restricted to those for snuff and for studies conducted in Scandinavia. Each of the three sets of meta-analyses is divided into overall data, smoking-adjusted and never smokers. In the overall data analyses, estimates are not restricted on smoking status or on adjustment for smoking. The smoking-adjusted analyses only include estimates that are for the whole population and adjusted for smoking or are for never smokers. The never smokers analyses are restricted to estimates for never smokers. For oropharyngeal cancer, where more estimates are available, some additional meta-analysis results are shown, based on estimates that are smoking and alcohol adjusted, and on estimates published since 1990.

To avoid double-counting multiple non-independent estimates from the same study, estimates from each study are selected for inclusion in the meta-analyses using order of preference lists for ST exposure (ever use/unspecified use/current use/former use), then smoking status (any – based on the combined population of smokers and non-smokers/never smokers), and then ST type (ST/snuff/chew), with each list being in order of most to least preferred. At each step we retain those estimates highest up the list, discarding any estimate lower in the preference order. If the procedure ends up with separate estimates for males and for females, both are included in the analysis. In one study [36], the results available are for males for chewing and for females for snuff (see Table Table3).3). Although the procedure, strictly applied, selects only the snuff estimate, it was decided to include both in the relevant meta-analyses.

Table 3
Oropharyngeal cancer; individual effect (relative risk/odds ratio) estimates

The presentation of the meta-analyses shows the number of estimates combined; the identification numbers of these estimates (so that they can be related to the preceding table of individual effect estimates); the combined random-effects estimate, with its 95% CI [116], the chi-squared and P value of homogeneity [119] and the I2 statistic [120]. The meta-analyses conducted also include a test for publication bias [121] where five or more estimates are combined. Findings significant at P < 0.1 are indicated.

Forest plots are also included for most of the cancers. These are generally based on the smoking-adjusted analyses, with the estimates split by region and shown with cohort data first, then case-control, presented in order of publication year.

Sensitivity analysis

For each estimate included, the value of Q2 is calculated by w (x - An external file that holds a picture, illustration, etc.
Object name is 1741-7015-7-36-i1.gif)2, where w is the inverse-variance weight, x is the logarithm of the effect size and An external file that holds a picture, illustration, etc.
Object name is 1741-7015-7-36-i1.gif its mean. Q2 is the contribution of the estimate to the heterogeneity chi-squared statistic [116]. Where there is significant (P < 0.05) heterogeneity of estimates, sensitivity to potentially outlying estimates is tested by removing that with the largest Q2 value and rerunning the analyses. This process is continued until there is no longer significant heterogeneity.

Sensitivity to the criterion for including estimates based on ST exposure is also tested by rerunning the meta-analyses with the preference list for ST exposure changed from ever use/unspecified use/current use/former use to current use/ever use/unspecified use/former use.

Meta-regression analysis

For oropharyngeal cancer, fixed-effects regression analysis is used to investigate how the estimates selected for the first set of meta-analyses vary by region (USA; Scandinavia; other), period × study type (cohort; case-control published before 1990; case-control published after 1990), sex (male; female; combined), ST exposure (ever or unspecified use; current use), smoking (any, adjusted for smoking; any, unadjusted for smoking; never) and alcohol adjustment (yes; no). For those other cancers where more than five estimates are available and where there was evidence of significant (P < 0.05) heterogeneity, the meta-regression analyses use a more limited variable list: region, sex, and smoking as above, and also study type (cohort; case-control).

Regression analyses are only conducted based on the overall data and smoking-adjusted data. The analyses successively introduce the most significant factor into the model, stopping when no further factor significant at P < 0.05 can be added. Significance is estimated by treating the ratio of the deviance per degree of freedom (d.f.) explained by the factor to the residual deviance per d.f. as an F statistic. For oropharyngeal cancer some additional analyses investigate the drop in deviance resulting from introducing each factor individually, and others are conducted having excluded 'outlying' observations with a very high Q2 value.

Estimating deaths attributable to smoking

RRs for current and former cigarette smokers (compared with never cigarette smokers) for men aged 35+ for seven major cancers caused by smoking (lip/oral cavity/pharynx, oesophagus, pancreas, larynx, lung, bladder, kidney/other urinary organs) were obtained from the American Cancer Society Cancer Prevention Study II (CPS-II) [122]. Numbers of deaths for these seven cancers occurring in US men aged 35+ in 2005 were obtained from WHO [123]. Estimates of the proportion of current and former cigarette smokers in US men aged 35+ in 2005 were obtained from the National Health Interview Survey [124].

Defining Di as the number of deaths for cancer i (i = 1,..., 7), Rci and Rfi as the RRs for current and former cigarette smokers for cancer i, and pc and pf as the proportions of current and former cigarette smokers in the population, the estimated number of deaths, An external file that holds a picture, illustration, etc.
Object name is 1741-7015-7-36-i2.gif, that would have occurred had the whole population the risk of never smokers, is then estimated by:

The number of deaths avoided from these seven cancers, had the whole population the risk of never smokers (that is, the deaths attributable to smoking) is then estimated by:

Estimating deaths attributable to ST in a population of never smokers

Let us further define Rsi as the estimated relative risk from ST for cancer i based on the meta-analyses using smoking-adjusted effect estimates. Where Rsi is estimated to be less than 1, it is taken to be 1 for the purposes of calculating deaths attributable to ST.

For a population of never smokers, the number of deaths from cancer i that would have occurred had the same proportion of men used ST as had ever smoked is then estimated by:

The increase in overall deaths from these seven cancers is then given by:

I1 can then be compared with E as an indicator of the relative effects of ST and smoking.

Also for a population of never smokers, the number of deaths from cancer i that would have occurred had all the men used ST, is estimated by:

The increase, compared with E, is then calculated by:


The MEDLINE search identified 690 publications. Two hundred and thirty-eight were rejected as describing studies conducted in Asia or Africa or relating to products typically used there, 96 as not describing epidemiological studies, 112 as not relating to cancer and 163 as being reviews, letters or comments not providing primary data. Seventeen were rejected as having an inappropriate study design and three as not providing relevant results. This left 61 apparently relevant publications. Taking into account also citations in recent reviews [1-6,10], and eliminating publications that referred to studies more recently or completely covered in other publications, a total of 104 publications were considered. Twenty-five related to nine cohort studies, and 79 to 80 case-control studies. Fuller details of the search are given in Figure Figure1,1, whilst the studies and publications considered are presented in the following two sections.

Figure 1
Flow chart for search strategy for review of literature on smokeless tobacco and cancer. The flow chart shows the number of publications identified by the MEDLINE search, and the number excluded by reason. The number of additional publications identified ...

Cohort studies

Results relating ST use to mortality or incidence have been reported for nine cohort studies, with results provided by multiple publications for some studies. Six studies have been conducted in the USA and are based on the Lutheran Brotherhood cohort [11-14], the US Veterans cohort [15-19], the Iowa cohort [20], the First National Health and Nutrition Examination Survey (NHANES I) Follow-up cohort [21,22], and the American Cancer Society Cancer Prevention Study I (CPS-I) [23] and Study II (CPS-II) [23-25]. One study was based on two Norway cohorts [14,26,27] while the remaining two were conducted in Sweden; one based on construction workers [28-34], and the other on a cohort in Uppsala County [35]. Fuller details of these studies are given in Table Table1.1. A number of these studies (US Veterans, CPS-I, CPS-II, Swedish Construction Workers) are extremely large, involving at least 100,000 subjects, though the number of ST users is less than this, particularly in the CPS-I and CPS-II studies where the analyses of Henley et al. [23] restricted attention to never smokers of cigarettes. The US studies generally present results for combined ST use, the main exception being the analyses of CPS-II [23] where some separate analyses are presented for snuff and chewing tobacco. The results from the Swedish studies relate to snuff use, as do the main results from the Norwegian study [26].

Case-control studies

Results relating ST use to cancer have been reported for 80 case-control studies, with Table Table22 providing details for each study, in chronological order of publication, of the location, period and controls, as well as the exposures, cancer types and sexes studied. Eighteen were published between 1920 and 1975 [36-52], 30 between 1976 and 1990 [53-82] and 32 between 1991 and 2007 [83-114]. In general there was one publication per study, but Bjelke [52] reported results from two studies, while the reference to Gross et al. [91] is to a review, which cites results from an unpublished study by Perry et al. Of the 80 studies, 56 were conducted in the USA, 11 in Sweden, three in each of Canada, Denmark and the UK, and one in each of Brazil, Norway and Puerto Rico, with one study conducted in five countries. Most of the studies involve only one or a small number of cancer types, but one study [55] involves a very wide range. The majority of the studies involve less than 1,000 cancer cases but 10 are larger than this [38,55,56,66,70,74,89,97,99,106]. The numbers of cancers in ST-exposed subjects are typically much lower than this, as will become evident when the results for the individual sites are presented. Of the different cancer sites, oral cancer is by far the most often studied. Of the 56 US studies, 11 provide results only for chewing tobacco, five only for snuff, and 18 only for ST, with the remaining 22 results for more than one type. Seven of the 11 studies in Sweden restricted attention to snuff, with three also considering chewing and one only considering chewing.

Adjustment for smoking

ST use is not a major subject for many of the publications from which results have been extracted. While reference is made to ST in the title of one or more papers relating to six of the nine cohort studies (NHANES I, CPS-I, CPS-II, Norway Cohorts, Swedish Construction Workers and Uppsala County), the same is true for only 15 of the 80 case-control studies. For many of the other studies [39,42,59,61,66,70,89,91,102,104,108,109,111,113,114], the reports only provide limited information about ST use in the text, simply giving percentages of users in the cases and controls or even saying there was an association or no association, but without giving supportive data. Many papers consider ST independently of smoking, with no attempt to adjust ST effect estimates for smoking, even though for many of the cancers considered smoking is known to be a cause, and often a major cause.

To summarise the extent to which the available effect estimates were adjusted for smoking, the studies were divided into five groups (A = no information, B = no adjustment, C = never smokers, D = some adjustment, E = more adjustment) as described more fully in the methods. Of the nine cohort studies, the numbers in the five categories were, respectively, 0, 1, 3, 3 and 2. The Iowa study [20] failed to take smoking into account at all, while the CPS-I and CPS-II studies [23] and the main results from NHANES I [22] were restricted to never smokers. In the remaining five cohort studies, the extent of smoking adjustment varied from publication to publication, but amount smoked or duration of smoking were never taken into account in the US Veterans, Norway cohorts and Uppsala County studies so they are classified as group D. In the Lutheran Brotherhood study, amount smoked was taken into account in the analyses of pancreatic cancer [13] and stomach cancer [12], and in the Swedish Construction Workers study, amount smoked was adjusted for in the analyses of stomach and oesophageal cancer [34], and cutaneous squamous cell carcinoma [29], and they are therefore classified as group E.

Of the 80 case-control studies considered, details of the adjustment factors used are not provided in either of the studies reported by Bjelke [52] or in two other studies [93,109] (category A). For a further 38 studies [36,38-40,42,44-46,49,51,53,54,56,57,59,60,63,64,67,70-73,75,78,80-82,84-86,92,95,96,98,100,103,110] the results available for ST are for the whole population, with no adjustment for smoking (category B). In 14 studies [43,47,48,66,69,74,76,83,87,88,99,101,111,112] the only relevant smoking-adjusted results reported are for never smokers (category C). In the remaining 24 studies, some smoking-adjusted results are available for the whole population. Fourteen of these [37,41,50,58,61,62,65,94,97,102,104,107,108,114] can be classified into category D. In only 10 reports [55,68,77,79,89-91,105,106,113], is some account taken of daily dose and/or duration of smoking (category E).

Oropharyngeal cancer

Table Table33 presents individual effect estimates from six cohort and 34 case-control studies, with 36 of the 40 studies providing estimates with CI that could be used in meta-analyses, the other four [40,71,86,92] finding no significant relationship. Thirty-eight of the 41 estimates included in the first meta-analysis (see Table Table4)4) are those given in our earlier review of ST and oral cancer [4], three recently published studies [32,35,113] being introduced into the current analysis. The overall data show an association with any ST use (1.79, 1.36–2.36) that, though highly significant, is based on an extremely heterogeneous set of estimates (P < 0.001). Limiting consideration to smoking-adjusted data, the estimate reduces substantially, to 1.36 (1.04–1.77, n = 19), though it is still significant, and marked heterogeneity remains (P < 0.001). Further limiting attention to estimates adjusted for both smoking and alcohol, the two major risk factors for oropharyngeal cancer [7,8], eliminates both heterogeneity and excess risk (1.07, 0.84–1.37, n = 10). A significant relationship is seen in never smokers (1.72, 1.01–2.94, n = 9), though the estimates are heterogeneous (P = 0.044), and generally based on a very small number of oropharyngeal cancer cases that used ST.

Table 4
Oropharyngeal cancer; meta-analysis results

When the analyses are restricted to US studies, the pattern is similar to that for the overall data, with the effect estimates reduced when attention is limited to those that are smoking-adjusted, and close to 1.0 when estimates that are adjusted both for smoking and alcohol are considered. The effect estimate for never smokers is significantly increased (3.33, 1.76–6.32), based on five small studies, in total involving 19 ST-exposed oropharyngeal cancer cases.

No real evidence of a relationship with snuff use is seen in studies conducted in Scandinavia, where seven estimates, all adjusted for smoking, and four additionally adjusted for alcohol, give a combined estimate of 0.97 (0.68–1.37). However some heterogeneity should be noted, a high RR of 3.1 (1.5–6.6) in the Uppsala County study [35] conflicting with six other estimates ranging from 0.67 to 1.10.

Many of the higher estimates seen in Table Table44 come from older studies which often did not adjust for smoking. If attention is limited to studies published since 1990, which generally did adjust, no association is seen. Indeed, the combined estimate from the 14 smoking-adjusted studies published since 1990 is 1.00 (0.83–1.20), and shows no significant heterogeneity.

While the choice of 1990 as the cut-point was not defined a priori, the change in estimates about that time is very clear. As shown in Figure Figure2,2, smoking-adjusted estimates for case-control studies published between 1920 and 1988 are consistently high (overall 2.38, 95% CI 1.87–3.04), while estimates for case-control studies published between 1991 and 2005 show no association at all (0.98, 0.83–1.16). There is no evidence of heterogeneity within either period (P = 0.34 for pre-1990 and P = 0.93 for post-1990) and a highly significant (P < 0.001) difference between estimates in the two periods. Smoking-adjusted estimates for the cohort studies which, though published between 2005 and 2008, generally cover a long follow-up period extending from before 1990, give an intermediate result (1.32, 0.65–2.68).

Figure 2
Smokeless tobacco and oropharyngeal cancer by study type and period of publication (smoking-adjusted data). The 19 individual smoking-adjusted relative risk (RR) and 95% confidence interval (CI) estimates separated by study type, and for case-control ...

The findings are very similar to those in an earlier review [4]. That review provides additional meta-analyses of the slightly smaller data set, further investigating variation by type of ST, sex, study design, study location and study period. It also provides full details of the various types of cancer that have been considered in the source papers.

The evidence presented suggests that snuff as used in Scandinavia has no effect on oropharyngeal cancer risk. Products used in the past in the USA may have increased the risk but any effect that exists now seems likely to be quite small.

Oesophageal cancer

Table Table55 summarises the data from four cohort and 10 case-control studies. For five of these studies effect estimates with CI are not available, one of these [52] reporting a 'synergistic effect of tobacco chewing and alcohol', another [19] presenting a RR of 2.28, but not whether it was significant, and the others [14,40,60] showing no significant relationship. Of the remaining nine studies, six provide smoking-adjusted estimates, three of which are also adjusted for alcohol. Though estimates are generally somewhat above 1.0 in these nine studies, they are rarely significant, exceptions being the estimate of 1.92 (1.00–3.68) for snuff in never smokers in the Swedish Construction Workers study [34] and that for chewing of 2.39 (1.23–4.64) in the Wynder and Bross case-control study [44].

Table 5
Oesophageal cancer; individual effect (relative risk/odds ratio) estimates

The meta-analyses (see Table Table66 and Figure Figure3)3) show some indication of an association, though this is not always statistically significant. Based on all available smoking-adjusted data, the combined estimate for any ST use is 1.13 (0.95–1.36, n = 7), somewhat lower than when there is no restriction to smoking-adjusted data (1.25, 1.03–1.51, n = 10). The corresponding analyses show no real indication of an effect for snuff in Scandinavia, but are more suggestive for the USA. Even here, the smoking-adjusted estimate is not significant (1.89, 0.84–4.25), though this is based on only three small studies, involving a total of 11 cases using ST. The estimates based on all the available smoking-adjusted data include an any smoking RR of 1.00 (0.79–1.27) from the study with the largest weight, the Swedish Construction Workers study [34], this RR being derived by combining the findings for adenocarcinoma and squamous cell carcinoma. The meta-analyses for never smokers give a higher combined estimate of 1.91 (1.15–3.17, n = 4) for any ST use, mainly because they use a higher (combined adeno/squamous) estimate of 1.92 (1.00–3.68) for the Swedish Construction Workers study [34].

Figure 3
Smokeless tobacco and oesophageal cancer by region (smoking-adjusted data). The seven individual smoking-adjusted relative risk (RR) and 95% confidence interval (CI) estimates, separated by region, are shown numerically and also graphically on a logarithmic ...
Table 6
Oesophageal cancer; meta-analysis results

Overall, the data must be regarded as providing suggestive evidence of a possible weak relationship between ST use and oesophageal cancer.

Stomach cancer

Table Table77 presents results from 12 studies, eight of which provide a total of 17 estimates which could be used in meta-analyses. Although the Swedish construction workers study [34] shows a significant increase in risk of stomach cancer associated with snuff use for never smokers (RR 1.33, 95% CI 1.03–1.72), no other significant associations are reported, and the meta-analyses conducted (see Table Table88 and Figure Figure4)4) are all non-significant. Based on smoking-adjusted estimates from eight studies, the combined RR estimate is 1.03 (95% CI 0.88–1.20). Four studies did not provide detailed data. No association with stomach cancer was reported by Weinberg et al. [67] or for the US data considered by Bjelke [52]. However, Bjelke did report an "Association ... with tobacco chewing" for the Norwegian data, and a standardised mortality ratio of 1.51 was given for the US Veterans' Study [19], but not whether this was statistically significant.

Figure 4
Smokeless tobacco and stomach cancer by region (smoking-adjusted data). The eight individual smoking-adjusted relative risk (RR) and 95% confidence interval (CI) estimates, separated by region, are shown numerically and also graphically on a logarithmic ...
Table 7
Stomach cancer; individual effect (relative risk/odds ratio) estimates
Table 8
Stomach cancer; meta-analysis results

The combined evidence does not indicate an effect of ST use on the risk of stomach cancer.

Pancreatic cancer

Table Table99 presents results from four cohort and seven case-control studies. For four of the studies effect estimates that can be included in meta-analyses are not available; two [75,84] of these studies merely reported finding no association, one [19] reported an elevated RR of 1.65 with no CI, and another [82] a reduced RR of 0.80, also with no CI. Of the other seven studies, significant increases have been reported in two. The Norway cohorts study [26] reports an increase in ever users of snuff in a smoking-adjusted analysis based on the whole population (1.67, 95% CI 1.12–2.50) but not in an analysis based on never smokers (0.85, 0.24–3.07). Conversely, the Swedish construction workers study shows no increase in a smoking-adjusted analysis based on the whole population (0.9, 0.7–1.2), but an increase in never smokers (2.0, 1.2–3.3). None of the three meta-analyses presented in Table Table1010 (see also Figure Figure5)5) for any ST use show any significant increase, though they all show evidence of heterogeneity. Smoking-adjusted overall population effect estimates are available for all seven studies considered, the combined estimate being 1.07 (0.71–1.60). For never smokers, the estimate is 1.23 (0.66–2.31, n = 5). No significant associations are seen in the separate meta-analyses for the USA and Scandinavia.

Figure 5
Smokeless tobacco and pancreatic cancer by region (smoking-adjusted data). The seven individual smoking-adjusted relative risk (RR) and 95% confidence interval (CI) estimates, separated by region, are shown numerically and also graphically on a logarithmic ...
Table 9
Pancreatic cancer; individual effect (relative risk/odds ratio) estimates
Table 10
Pancreatic cancer; meta-analysis results

At most, the overall data weakly suggest a possible effect of ST on pancreatic cancer risk. A fuller discussion of these data is available elsewhere [5].

Other cancers of the digestive system

Table Table1111 summarises evidence relating to cancers of the digestive system other than those considered already in Tables Tables5,5, ,77 and and9.9. Nine studies are considered, four cohort and five case-control, with one or two studies providing data for colon cancer, rectal cancer, colorectal cancer, small intestine cancer, liver cancer, gall bladder and bile duct cancer. These data, which are insufficient for meta-analysis, include two statistically significant effect estimates: an RR of 1.9 (1.2–3.1) for rectal cancer and ST use from the US Veterans study [18] and a remarkably high OR from the case-control study of Chow et al. [93] of 18.0 (1.4–227.7) for bile duct cancer and chewing tobacco, based on only three exposed cases.

Table 11
Other cancers of the digestive system; individual effect (relative risk/odds ratio) estimates

There are rather more data for the combined category of all cancers of the digestive system. Of the four studies providing data, all conducted in the USA, NHANES I [22] and CPS-II [23] show no relationship, CPS-I [23] a weak, but significant, positive relationship, and the case-control study of Sterling et al. [89] a significant negative relationship. Overall, the combined estimate (see Table Table1212 and Figure Figure6),6), all based on smoking-adjusted data, is 0.86 (0.59–1.25, n = 5), with significant evidence of heterogeneity (P = 0.002). The analysis for never smokers removes the case-control study and eliminates the heterogeneity. However the combined estimate of 1.14 (0.99–1.33, n = 4) remains non-significant.

Figure 6
Smokeless tobacco and overall digestive cancer (USA smoking-adjusted data). The five individual relative risk (RR) and 95% confidence interval (CI) estimates, all smoking-adjusted and for the USA, are shown numerically and also graphically on a logarithmic ...
Table 12
Overall digestive cancer; meta-analysis results

More data are needed before any conclusion can be drawn for these cancers.

Larynx and nasal cancer

The data shown in Table Table1313 are quite limited. The evidence for nasal cancer is based on only three studies, none reporting a significant association with ST use. Seven studies investigated the relationship of ST to larynx cancer, two providing no effect estimates and merely reporting a lack of association. Control for confounding variables is very limited, with only two studies providing estimates adjusted for smoking, only one adjusting for alcohol and no study presenting any results for never smokers. The only study to adjust for smoking and alcohol [102], which shows no relationship of snuff to risk of larynx cancer, is the only study conducted in Scandinavia. Two US studies [55,56] report a significant relationship, however, and, as shown in Table Table1414 (see also Figure Figure7),7), an association is seen in the overall data (1.43, 1.08–1.89, n = 5).

Figure 7
Smokeless tobacco and larynx cancer by region (overall data). The five individual relative risk (RR) and 95% confidence interval (CI) estimates, separated by region, are shown numerically and also graphically on a logarithmic scale. They are sorted in ...
Table 13
Larynx and nasal cancer; individual effect (relative risk/odds ratio) estimates
Table 14
Larynx and nasal cancer; meta-analysis results

Given the independent role of smoking and alcohol in larynx cancer [7,8], and the lack of association in the one study that has adjusted for both these factors [102], any independent association of ST use with larynx cancer risk has not been established. More data are needed before any conclusion can be drawn on the role of ST in larynx and nasal cancers.

Lung cancer

Table Table1515 summarises data from six cohort and three case-control studies. The case-control studies provide only estimates for smokers and non-smokers combined, and only one of these is adjusted for smoking. The cohort studies all provide estimates for never smokers, with two also giving smoking-adjusted results for the overall population. The meta-analyses (see Table Table1616 and Figure Figure8)8) show no evidence that ST use increases risk of lung cancer, with the combined estimate for smoking-adjusted data 0.99 (95% CI 0.71–1.37). However, there is considerable heterogeneity (P < 0.001), the major contributors to this being the high RR of 6.80 (1.60–28.5) in never smokers in NHANES I [22], the significant increase of 1.77 (1.14–2.74) from CPS-II [23], and the low RR of 0.70 (0.60–0.70) for the Swedish construction workers study [32]. While the combined estimate for never smokers for any ST use is greater than 1.0 (1.34, 0.80–2.23, n = 5), it is not statistically significant.

Figure 8
Smokeless tobacco and lung cancer by region (smoking-adjusted data). The six individual smoking-adjusted relative risk (RR) and 95% confidence interval (CI) estimates, separated by region, are shown numerically and also graphically on a logarithmic scale. ...
Table 15
Lung cancer; individual effect (relative risk/odds ratio) estimates
Table 16
Lung cancer; meta-analysis results

While the data have unexplained heterogeneity, they do not provide any clear indication of a relationship of lung cancer to ST use.

Not included in Table Table1515 are results from an analysis conducted by Henley et al. in 2007 [25] based on follow-up of the CPS-II cohort from 1982 to 2002. They report an increased risk of lung cancer (1.46, 1.24–1.73) in men who switched from cigarette smoking to ST compared with those who quit entirely, after adjusting for age, other demographic variables, as well as variables associated with smoking history. This analysis may be biased by reliance on tobacco use data recorded in 1982, and by residual confounding, with the paper reporting marked differences between switchers and quitters in a range of characteristics, with adjustment substantially reducing the RR estimate from the age-adjusted estimate of 1.92 (1.63–3.26).

Prostate cancer

Table Table1717 presents data from five cohort and two case-control studies, all conducted in the USA. No significant association between ST and prostate cancer is evident in five studies, but significant increases are seen in the Lutheran Brotherhood Study [11] and, for current snuff users only, in the case-control study by Hayes et al. [96]. Based on the five studies which provide usable data, the overall estimate (see Table Table1818 and Figure Figure9)9) is 1.20 (95% CI 1.03–1.40).

Figure 9
Smokeless tobacco and prostate cancer (USA overall data). The five individual relative risk (RR) and 95% confidence interval (CI) estimates, all for the USA, are shown numerically and also graphically on a logarithmic scale. They are sorted in order of ...
Table 17
Prostate cancer; individual effect (relative risk/odds ratio) estimates
Table 18
Prostate cancer; meta-analysis results

Prostate cancer is not considered smoking related [7,8], and more information on its relationship with ST is needed before any clear conclusion can be drawn.

Bladder cancer

Table Table1919 summarises data from the Norway cohorts study [26] and from 12 case-control studies. None of the case-control studies were conducted after 1990, and with the exception of two studies in Denmark [43,62], all were carried out in the USA or Canada. The great majority of the estimates are non-significant, and based on 10 smoking-adjusted estimates the overall estimate (see Table Table2020 and Figure Figure10)10) is 0.95 (95% CI 0.71–1.29). However, there is significant heterogeneity due mainly to estimates 8, 12 and 22, which show a positive association, the last two of which are significant, and estimate 31 which shows a significant negative association.

Figure 10
Smokeless tobacco and bladder cancer by region (smoking-adjusted data). The 10 individual smoking-adjusted relative risk (RR) and 95% confidence interval (CI) estimates, separated by region, are shown numerically and also graphically on a logarithmic ...
Table 19
Bladder cancer; individual effect (relative risk/odds ratio) estimates
Table 20
Bladder cancer; meta-analysis results

Considered together, the data provide no real evidence of an association between ST and bladder cancer.

Kidney cancer

Table Table2121 summarises evidence from one cohort and nine case-control studies, none conducted in Sweden. The estimates are generally based on small numbers of cases using ST, and are variable, with four studies [47,68,73,100] providing a statistically significant OR estimate exceeding 3.0, and other studies (and other estimates from the four studies) showing notably smaller estimates, that are not significant. Most of the meta-analysis estimates shown in Table Table2222 (see also Figure Figure11)11) are elevated, with some evidence of heterogeneity, but none are statistically significant. Based on five smoking-adjusted estimates the overall estimate for any ST use is 1.09 (0.69–1.71).

Figure 11
Smokeless tobacco and kidney cancer by region (smoking-adjusted data). The five individual smoking-adjusted relative risk (RR) and 95% confidence interval (CI) estimates, separated by region, are shown numerically and also graphically on a logarithmic ...
Table 21
Kidney cancer; individual effect (relative risk/odds ratio) estimates
Table 22
Kidney cancer; meta-analysis results

While there is a suggestion of a possible relationship, more data are needed before any firm conclusions can be reached.

Haematopoietic and lymphoid cancer

Table Table2323 summarises evidence from three cohort and seven case-control studies for overall haematopoietic cancer and for specific types. The only report of a significant association is the OR of 4.0 (1.3–12.0) for non-Hodgkin's lymphoma in the case-control study of Bracci and Holly [112]. However, the combined evidence from the five studies (see Table Table2424 and Figure Figure12)12) for non-Hodgkin's lymphoma shows no significant relationship (1.20, 0.83–1.75), though there is significant heterogeneity (P = 0.01), due mainly to the Bracci and Holly estimate. The evidence for other endpoints – multiple myeloma, Hodgkin's disease, leukaemia, and overall haematopoietic cancer – is more limited, and does not suggest any relationship with ST use.

Figure 12
Smokeless tobacco and non-Hodgkin's lymphoma by region (overall data). The five individual relative risk (RR) and 95% confidence interval (CI) estimates, separated by region, are shown numerically and also graphically on a logarithmic scale. They are ...
Table 23
Haematopoietic and lymphoid cancer; individual effect (relative risk/odds ratio) estimates
Table 24
Non-Hodgkin's lymphoma; meta-analysis results

Other cancers

Table Table2525 summarises evidence from six cohort and four case-control studies relating to cancers of types not considered in Tables Tables33 to to24.24. Most of the results relate to specific cancer types, though some relate to broader groupings, such as genitourinary cancer and smoking-related cancer, which include cancer types considered earlier. Due to the variety of types, and the limited numbers of estimates relating to any one type, no meta-analyses were attempted. One of the studies [109] simply reported a lack of association (with glioma), and the remaining studies provided a total of 24 effect estimates with CI. Six of these are statistically significant. Zahm et al. [81] report an age-adjusted OR of 1.80 (95% CI 1.10–2.90) for soft tissue sarcoma based on a case-control study, though fail to confirm this later using data from the US Veterans Study [17]. The Williams and Horm study [55] provides a smoking-adjusted estimate of 4.18 (2.08–8.43) for cancer of the cervix, no other study giving relevant results. Moore et al. [39], in a study conducted in 1953, report a crude estimate of 2.41 (1.09–5.35) for cancer of the face, again an endpoint not considered by others. Roosaar et al. [35] report an increased risk of smoking-related cancer (1.6, 1.1–2.5) for never smokers, but not in a smoking-adjusted analysis for smoker and non-smokers combined (1.1, 0.8–1.4). Finally, based on the Swedish construction workers study, Odenbro et al. [29,33] report that snuff use is associated with a reduced smoking-adjusted risk of cutaneous squamous cell carcinoma (0.64, 0.44–0.95) and, in never smokers, with a reduced risk of melanoma (0.65, 0.52–0.82). These isolated reports need confirmation in other studies before any effect of ST can reliably be inferred. A study in Cherokee women [125,126] which shows no association of breast cancer with ever ST use, with an odds ratio adjusted for age at diagnosis estimated as 1.24 (0.26–6.02), is not considered in Table Table2525 as the study is of cross-sectional design. It contributes little to the evidence.

Table 25
Other cancers; individual effect (relative risk/odds ratio) estimates

Overall cancer risk

As shown in Table Table26,26, ST use has been related to overall cancer risk in five cohort studies and one case-control study. Two of the 12 estimates shown are smoking-adjusted estimates for smokers and non-smokers combined, one (estimate 10) showing no association at all (RR = 1.00) and the other (estimate 12, based on the case-control study [89]) a reduced OR of 0.64 (95% CI 0.53–0.78). The remaining 10 estimates, all from cohort studies, and all adjusted for age and various other potential confounders, are for never smokers. As shown in Table Table2727 and Figure Figure13,13, the combined estimate for all the smoking-adjusted data is not elevated (0.98, 0.84–1.15, n = 7). However, the combined estimate for never smokers, which excludes the low estimate from the case-control study, is a significant 1.10 (1.02–1.19, n = 6). The estimate for never smokers is similar for the US data (1.10, 1.01–1.20, n = 4) and the Scandinavian snuff data (1.10, 0.94–1.29, n = 2). The data are consistent with any excess risk of cancer in ST users being small.

Figure 13
Smokeless tobacco and overall cancer by region (smoking-adjusted data). The seven individual smoking-adjusted relative risk (RR) and 95% confidence interval (CI) estimates, separated by region, are shown numerically and also graphically on a logarithmic ...
Table 26
Overall cancer; individual effect (relative risk/odds ratio) estimates
Table 27
Overall cancer; meta-analysis results

Publication bias

There are 49 meta-analyses presented that combine five or more effect estimates. The test of publication bias [121] shows none to be significant at P < 0.01, and two significant at P < 0.05, similar to the numbers one would expect by chance. Both the significant cases (see Tables Tables2222 and and24)24) arise due to a single high effect estimate, with the other estimates included in the analysis relatively close to 1.0.

Sensitivity analyses

Table Table2828 shows the effect on the smoking-adjusted analyses of successively removing those RR/OR estimates with the largest Q2 values. Results are only shown for those cancers where significant (P < 0.05) heterogeneity was evident, and removal continues until no significant heterogeneity is seen. For pancreatic, lung and bladder cancer and for non-Hodgkin's lymphoma, only relatively high estimates are removed, and the random-effects estimate decreased, though only for lung cancer was the estimate now significantly below 1.0. For digestive cancer, the effect is to increase the estimate, but the significance is unchanged. For overall cancer, the effect is also to increase the estimate, here to marginal significance, 1.07 (1.00–1.15). For oropharyngeal cancer, the original substantial heterogeneity (P < 0.001) is seen to be due mainly to four estimates, three high and one low. The excess decreases from a significant 1.36 (1.04–1.77) to a non-significant 1.17 (0.95–1.45) after the removal of these estimates.

Table 28
Sensitivity analyses for smoking-adjusted data. Effect of removing relative risk/odds ratio estimates with largest Q2 values on heterogeneity and random-effects meta-analysis estimates

Similar analyses for the overall data (not shown) were also carried out. They also did not help to demonstrate any clear effect of ST on risk. For oropharyngeal cancer, where heterogeneity is very marked indeed, this is mainly due to estimates with atypically high values (see particularly Table Table33 id. numbers 1, 15, 21, 22, 34 and 35).

Table Table2929 compares the smoking-adjusted meta-analysis estimates reported earlier with those recalculated preferring, where there was a choice, estimates for current ST use to those for ever use or unspecified ST use. The meta-analyses for the 12 cancers considered are based on a total of 83 effect estimates. In only 19 of these (23%) did the change in order of preference affect the estimate chosen. For 10 of these the estimate for current ST use is higher than that for ever or unspecified use, for eight it is lower, and for the other the two estimates are the same. The largest change is for pancreatic cancer in the Swedish construction workers study [32], where the selected RR value increases from 0.90 (0.70–1.20) in the original analysis to 2.10 (1.20–3.60) in the sensitivity analysis. However most of the changes, in either direction, are quite minor.

Table 29
Further sensitivity analyses for smoking-adjusted data. Effect of preferring estimates for current smokeless tobacco use to those for ever or unspecified smokeless tobacco use

For 8 of the 12 cancers, the change to the meta-analysis estimate from the altered preference is very small, by ± 0.02 at most. For oropharyngeal cancer it increases by 0.06, for larynx cancer by 0.11, for lung cancer by 0.12 and for pancreatic cancer 0.15. None of these changes materially affect the significance or the interpretation. Although there is perhaps a slight indication that associations may be stronger for current use, the tendency of most studies to report results only for ever or unspecified ST use limits the extent to which this can be investigated. Changing preferences did not materially affect the heterogeneity of the estimates. The effect of similarly changing the preference on the other meta-analyses shown earlier (for example, for never smokers or by country) also did not materially affect the results obtained (data not shown).

Meta-regression analyses

For oropharyngeal cancer, based on the 19 smoking-adjusted estimates, where the deviance (heterogeneity χ2) is 69.5 (P < 0.001), significant reductions in deviance in 'one factor at a time' analysis are seen for period by study type (P < 0.001, drop in deviance 46.7 on 2 d.f.), sex (P = 0.020, drop 26.9 on 2 d.f.) and region (P = 0.014, drop 21.3 on 1 d.f.). However, the tendency for estimates to be high in females and the USA was no longer significant after adjustment for period by study type, this relationship reflecting the tendency for estimates to be high in case-control studies published before 1990, low in case-control studies published after 1990, and intermediate in prospective studies (see Figure Figure22).

Based on the 41 overall estimates (whether smoking-adjusted or not) for oropharyngeal cancer, where the deviance is 335.6 (P < 0.001), the most significant factor is sex (P = 0.004, drop 83.4 on 2 d.f.). Though drops in deviance of 20 or more are also seen for region, period by study type and smoking status, with estimates high for females, USA, old case-control studies and data unadjusted for smoking, no other factor is significant at P < 0.05 after adjustment for sex. The high deviance of 335.6 is clearly due to very high Q2 values for some estimates, and further analyses were run excluding these estimates (ids 1, 7, 21, 22 and 34 in Table Table3).3). This reduces the deviance considerably, to 84.4, though it is still highly significant (P < 0.001). However, again sex was the most significant factor (P = 0.02), with no further factor significant at P < 0.05 after adjusting for sex.

Meta-regression analyses were not attempted for larynx, nasal or prostate cancer or for overall digestive cancer or non-Hodgkin's lymphoma because of insufficient numbers of estimates, or for oesophageal, stomach and kidney cancer because of lack of heterogeneity. For pancreatic and bladder cancer, none of the factors investigated significantly (at P < 0.05) explained the heterogeneity. For overall cancer, study type was significant (P = 0.001), but this merely reflected the low estimate for the single case-control study, evident also in the sensitivity analysis shown in Table Table28.28. For lung cancer, a tendency was noted for never-smoking estimates to be high, significant for both the smoking-adjusted data (P = 0.025) and the overall data (P = 0.029). This difference reflected the two high estimates already noted in the sensitivity analysis.

Summary of meta-analyses for ST use in Western populations

Table Table3030 brings together all the meta-analysis results for ST use in Western populations. Based on smoking-adjusted data, significant increases (P < 0.05) are seen for oropharyngeal cancer, though not based on studies published since 1990, and for prostate cancer, but not for any other cancer considered. For never smokers, significant increases are seen for oropharyngeal cancer (again not when based on studies published since 1990), for oesophageal cancer and also for overall cancer. Compared with the smoking-adjusted estimates, the estimates for never smokers tend to be more variable, due to smaller numbers of ST-exposed cases studied, though they consistently exceed 1.0.

Table 30
Summary of meta-analyses for smokeless tobacco use in Western populations

Summary of meta-analyses for ST use in the USA

Table Table3131 similarly brings together the results for ST use in the USA. With the exception of oesophageal cancer in never smokers, significant increases seen in Table Table2828 are again significant here, with an increase additionally seen in the smoking-adjusted estimate for larynx cancer (although based on only a single study).

Table 31
Summary of meta-analyses for smokeless tobacco use in the USA

Summary of meta-analyses for snuff use in Scandinavia

As shown in Table Table32,32, the meta-analyses of results provide overall effect estimates that, with one exception, are never significantly increased and generally are close to 1.00. The exception is for oesophageal cancer, where the marginally significant increased RR seen in relation to snuff use for never smokers (1.92, 1.00–3.68) derives solely from the Swedish Construction Workers study [34]. In that study, no increase was seen in smoking-adjusted analyses for the whole population (1.00, 0.79–1.27). Unlike the corresponding results for the USA, where meta-analysis estimates are predominantly greater than 1.0, the estimates for snuff as used in Scandinavia are as often below 1.0 as above 1.0. Generally, the results do not suggest that snuff as used in Scandinavia has any adverse effect on cancer risk.

Table 32
Summary of meta-analyses for snuff as used in Scandinavia

Dose response data

Results relating the various cancers to dose of exposure to ST are only reported in a few studies and are not presented in detail here.

For oropharyngeal cancer, eight studies were identified that related risk to extent and/or duration of exposure. In seven of these studies, which all show no overall relationship of ST with risk in Table Table33[32,55,89-91,104,113], no significant dose-response relationships are seen. It was only in one study [61], that did show a clear overall relationship, that a significant (P < 0.001) trend in risk with increasing duration of exposure is seen, though only for cancers of the gum and buccal mucosa, and not for other mouth and pharynx cancers.

For other cancer sites relatively few studies report dose-response data. In the CPS-II study [23] no trends with duration or frequency are seen for either total or lung cancer, while in the Swedish Construction Workers study no trend is seen for cutaneous squamous cell carcinoma with years of snuff dipping [29] or for oral cancer or lung cancer with daily amount of snuff consumed [32]. A significant trend (P < 0.01) is reported with daily amount of snuff consumed for pancreatic cancer [32] in never smokers, but this merely reflects the overall relationship, with RRs similar in light and heavy users (1.9 for 1–9 g/day, and 2.1 for 10+ g/day relative to never users). For some of the case-control studies considered [38,44,53,55,89,96,100,104,108,110,111,114], dose-response results are available, but these generally show no significant trends. The only exceptions are a study of kidney cancer [100] which reports a significant (P < 0.05) trend for risk to increase with frequency of use of chewing tobacco, and a study of pancreatic cancer [111] which reports a significant (P = 0.04) trend for risk to increase with ounces per week (oz/wk) ST used, though with the odds ratios forming an erratic pattern (1.0 for nonusers of tobacco, 0.3 for ≤ 2.5 oz/wk ST and 3.5 for > 2.5 oz/wk ST). Generally the rather sparse dose-response data add little to the overall evidence.

Comparison of the effects of smoking and of ST use

Table Table3333 summarises the results of analyses comparing the effects of smoking and of ST use, for seven smoking-related cancers [127]. Overall in US men aged 35+ a total of 142,205 deaths were seen from these cancers in 2005, with lung cancer (63.4%) by far the most common. Based on RRs from CPS-II for current and former smoking [122] and estimates of the frequency of current and former smoking [124] for US men of this age group, the total number of deaths that would have occurred if the men had the mortality rates of never smokers can be estimated as 37,468, a reduction (E) of 104,737 deaths. This reduction is proportionately largest for the cancers most strongly associated with smoking (lung and oropharynx), and least for those most weakly associated (pancreas, kidney and bladder).

Table 33
Comparison of effects of smoking and smokeless tobacco on smoking-related cancera in US males aged 35+

The smoking-adjusted relative risks for any ST use taken from Table Table3030 are then used to estimate the number of deaths that would have occurred if the population were never smokers, with ST use either at the same frequency as for current and former smoking combined, 53%, or at 100%. In the first situation, the number of cancer deaths rises from 37,468 to 38,570, an increase of 1,102; in the second situation, it rises to 39,548, an increase of 2,081. These numbers of cancers associated with ST use form, respectively, 1.1% and 2.0%, of E, the number associated with smoking.


Estimating the effects of ST use

We have analysed data relating cancer risk to the consumption of chewing tobacco and snuff as used in Western countries. We have identified 12 cancers (or combined categories) where, as shown in Table Table30,30, it is possible to derive a (random-effects) meta-analysis estimate based on at least five individual independent estimates.

It is notable that no strong association at all is evident and that few of the associations are significant at P < 0.05. Indeed, based on smoking-adjusted data, which might be argued to provide a good compromise between avoidance of bias and loss of power, only the estimates for oropharyngeal and prostate cancer are significant, with that for oropharyngeal cancer not evident in more recently published studies. However, it should be noted that while many of the estimates in Table Table3030 for never smokers have wide confidence limits, and only those for oropharyngeal and oesophageal cancer and for overall cancer are significant, all the estimates are in fact greater than 1.00. Although publication bias may be relevant, and more data are clearly needed, the consistency of these findings suggests that ST may increase the risk of cancer, though any effect is likely to be quite weak. The results in Table Table3232 suggest, however, that whether smoking-adjusted data or data for never smokers are considered, there is little or no evidence of an effect of snuff as used in Scandinavia.

There are a number of difficulties in interpreting the results of these meta-analyses. The studies are of varying design, size and quality. Many of the individual study reports have limitations and present less information than is ideal for a meta-analysis. Shortcomings include small numbers of cases, and in particular of cases exposed to ST, lack of histological confirmation, lack of division by cancer site, as well as an unclear description of inclusion and exclusion criteria, details of case and control selection, and methods of exposure assessment. Furthermore, details such as the type of ST used, and duration and frequency of use, are often not considered. The products used vary by country and over time, and increased risks seen in older studies for some cancers may not reflect the risks of more modern products, with reduced nitrosamine levels [128]. For most cancers, the number of effect estimates available is really too limited to allow a very detailed examination of variation in risk by such factors as type of product used, current or former use, country and sex. Though meta-regressions have been attempted for a number of cancers, they have not added materially to the interpretation, partly because of the limited amount of data for some cancers, and partly because of the number of apparently outlying estimates, notably for oropharyngeal cancer.

A major problem is that many of the studies fail to adjust for smoking and other important potential confounding variables. Although recent major reviews [7,8] consider that all the cancers considered in Table Table30,30, with the exception of prostate cancer and non-Hodgkin's lymphoma, are caused by smoking, it is evident that a number of the studies do not provide estimates that are either for never smokers or for smokers and non-smokers combined with adjustment for smoking. Even where adjustment for smoking is carried out, this is often by a relatively simple approach, with no account taken of number of cigarettes smoked or duration of smoking. Smokers who also use ST may smoke fewer cigarettes a day than smokers who do not. Failure to adjust for smoking is particularly common for studies of oropharyngeal cancer, with many of the older studies not taking smoking into account at all when considering ST. The potential importance of this is illustrated by the overall estimate for oropharyngeal cancer being substantially reduced, from 1.79 to 1.36, when attention is restricted to smoking-adjusted data.

Adjustment for other risk factors is also important, as shown by the case of oropharyngeal cancer where the smoking-adjusted estimate of 1.36 (1.04–1.77, n = 19) can be compared with the estimate adjusted for smoking and alcohol of 1.07 (0.84–1.37, n = 10). Restricting attention to estimates adjusted for both factors also eliminated the highly significant (P < 0.001) heterogeneity seen in the smoking-adjusted data. Alcohol is also an important factor in the aetiology of oesophageal, larynx and liver cancer [8], but the number of ST effect estimates adjusted both for smoking and alcohol for these three cancers is very low indeed, respectively 2, 1 and 0. Other factors considered rarely, or not at all, include, for example, Helicobacter pylori infection for stomach cancer and diet for digestive cancer.

Another difficulty in interpreting the overall results is the variability of the findings. Heterogeneity significant at least at P < 0.05 is evident in the smoking-adjusted estimates for cancers of the oropharynx (though not in the more recent data), pancreas, larynx, lung and bladder, as well as for overall cancer and overall digestive cancer. As noted above, the evidence is too limited for most of the cancers to allow a proper investigation of the sources of this heterogeneity.

Based on the data analysed, there is little or no evidence of publication bias. However, it should be noted that the number of studies reporting results in a form that cannot be included in the meta-analyses is fairly high, representing up to about 30% for some cancers (see Tables Tables5,5, ,7,7, ,9,9, ,1313 and and1717).

We are aware that the smoking-adjusted meta-analysis estimates we report for oropharyngeal cancer (1.36, 95% CI 1.04–1.77)), oesophageal cancer (1.13, 0.95–1.36), pancreatic cancer (1.07, 0.71–1.60) and lung cancer (0.99, 0.71–1.37) show much less evidence of a relationship with ST than do corresponding estimates recently reported in a review by Boffetta et al. [6] (oropharynx: 1.8, 1.1–2.9; oesophagus: 1.6, 1.1–2.3; pancreas: 1.6, 1.1–2.2; lung 1.2, 0.7–1.9). Reasons for this, based on a detailed analysis of this review, will be presented in a separate publication in BMC Cancer.

Comparison of the effects of smoking and ST use

In 2005 in US men aged 35 or over, there were a total of 142,205 deaths from seven cancers considered to be caused by smoking. Based on relative risks from CPS-II for current and former smoking [122] and estimates of the frequency of current and former smoking [124] for US men of this age group, we estimate that, had the population at risk the mortality rates of never smokers, the numbers would have reduced by 104,737, with the reduction in lung cancer deaths, 79,195, a major contributor. Any increase in risk resulting from the introduction of ST to a population of never smokers would be very much less than this. Even assuming that the smoking-adjusted meta-analysis estimates for the seven cancers all reflect a true effect of ST, the increase in deaths among a never-smoker population would be by 1,102 if 53% of the population used ST (the same proportion as had ever smoked) or by 2,081 if the whole population did. These increases represent, respectively, only 1.1% and 2.0% of the 104,737 deaths attributed to cigarette smoking.

There are a number of objections that can be made in respect of this comparison. These include the following:

1. The RRs for current and former smoking are based on CPS-II, conducted in the 1980s, and may not reflect those appropriate for 2005, given inter alia changes in cigarettes that have occurred since then. However, CPS-II is widely used as a source of data for calculating deaths attributed to smoking (for example, [8,129]).

2. The RR estimates used for ST use are not specifically for the USA, or for males. However, 62 of the 89 studies considered in this review were conducted in the USA, and 41 of the 58 estimates used in the smoking-adjusted meta-analyses for the seven cancers are for males (with 12 for sexes combined and five for females).

3. The RR estimates used for ST are for any ST use, and do not separate current and former use, due to most studies not providing such data.

4. The calculations are limited to those seven cancers which the US Surgeon General, in his 1989 report [122] considered to be caused by smoking and for which RRs were provided for CPS-II. A more recent report [8] includes stomach cancer and leukaemia as caused by smoking. For stomach cancer, the meta-analyses in Table Table66 showed virtually no association with ST use (1.03, 0.88–1.20, n = 8), while the more limited data for leukaemia also showed no clear evidence of a relationship.

5. It is theoretically possible that ST use might increase the risk of some cancers not increased by smoking. Here one should note the significant association for prostate cancer (1.29, 1.07–1.55).

6. The calculations do not take into account the fact that a proportion of US males aged 35+ already use ST. Given the relatively weak association between cancer and ST use, any attempt to do this would have had relatively little effect.

7. The calculations also do not take pipe and cigar smoking into account.

8. The approach used is somewhat simplistic, and a more realistic (but more complex) calculation might be to compare predicted cancer deaths over a long-term period in a population continuing to smoke as at present, with the predicted number in a population switching from cigarettes to ST.

Despite all these points, it is clear that any effect of ST on risk of cancer, if it exists at all, is quantitatively very much smaller than the known effects of smoking. This is in any case apparent from a simple comparison of the RRs for cigarette smoking and for ST use.


The available data relating to ST use have a number of weaknesses, including inadequate control for smoking in many, and limited data for never smokers. Nevertheless, it is possible to conduct meta-analyses based on smoking-adjusted estimates for a relatively wide range of cancers. These show no indication of an increased risk of cancer for snuff, as used in Scandinavia. The overall data for oropharyngeal cancer shows a significant increase in risk associated with ST use, but this is not evident for estimates adjusted for smoking and alcohol, or for studies published since 1990. Any effect of ST may relate mainly to products used in the past in the USA. A weak but significant association with prostate cancer, based on limited data from US studies, requires more confirmatory evidence. Reports of significant associations with pancreatic and oesophageal cancer in an earlier review [6] are not confirmed, and reasons for this will be discussed in a later publication. Risk from ST products as used in North America and Europe is clearly very much less than that from smoking, and is not evident at all in Scandinavia.


CI: 95% confidence interval; CPS-I: American Cancer Society Cancer Prevention Study I; CPS-II: American Cancer Society Cancer Prevention Study II; d.f.: degrees of freedom; NHANES I: First National Health and Nutrition Examination Survey; OR: odds ratio; RR: relative risk; ST: smokeless tobacco.

Competing interests

PNL, founder of PN Lee Statistics and Computing Ltd., is an independent consultant in statistics and an advisor in the fields of epidemiology and toxicology to a number of tobacco, pharmaceutical and chemical companies. JH works for PN Lee Statistics and Computing Ltd.

Authors' contributions

PNL previously contributed to reviews of some of the data considered here [4,5,10]. He planned the study and carried out the literature search. PNL and JH jointly extracted the estimates and conducted the meta-analyses. The text and tables were drafted by PNL and checked by JH. Both authors read and approved the final manuscript.

Pre-publication history

The pre-publication history for this paper can be accessed here:



Funding for this publication was provided by the European Smokeless Tobacco Council. Some previous related work was funded by Philip Morris International. This is an independent scientific assessment and the views expressed are those of the authors. We thank Pauline Wassell and Diana Morris for typing the various drafts of this paper and Yvonne Cooper who assisted in obtaining the relevant literature. Barbara Forey and John Fry commented on drafts of the paper.


  • Critchley JA, Unal B. Health effects associated with smokeless tobacco: a systematic review. Thorax. 2003;58:435–443. doi: 10.1136/thorax.58.5.435. [PMC free article] [PubMed] [Cross Ref]
  • International Agency for Research on Cancer. Smokeless tobacco and some tobacco-specific N-nitrosamines. [IARC Monographs on the evaluation of carcinogenic risks to humans.] Vol. 89. Lyon, France: IARC; 2007. http://monographs.iarc.fr/index.php [PubMed]
  • Scientific Committee on Emerging and Newly Identified Health Risks (SCENIHR) Health effects of smokeless tobacco products. Brussels: European Commission, Health & Consumer Protection Directorate-General; 2008. http://ec.europa.eu/health/ph_risk/committees/04_scenihr/docs/scenihr_o_013.pdf
  • Weitkunat R, Sanders E, Lee PN. Meta-analysis of the relation between European and American smokeless tobacco and oral cancer. BMC Public Health. 2007;7:334. doi: 10.1186/1471-2458-7-334. [PMC free article] [PubMed] [Cross Ref]
  • Sponsiello-Wang Z, Weitkunat R, Lee PN. Systematic review of the relation between smokeless tobacco and cancer of the pancreas in Europe and North America. BMC Cancer. 2008;8:356–368. doi: 10.1186/1471-2407-8-356. [PMC free article] [PubMed] [Cross Ref]
  • Boffetta P, Hecht S, Gray N, Gupta P, Straif K. Smokeless tobacco and cancer. Lancet Oncol. 2008;9:667–675. doi: 10.1016/S1470-2045(08)70173-6. [PubMed] [Cross Ref]
  • International Agency for Research on Cancer. Tobacco smoke and involuntary smoking. [IARC Monographs on the evaluation of carcinogenic risks to humans.] Vol. 83. Lyon, France: IARC; 2004. http://monographs.iarc.fr/ENG/Monographs/vol83/mono83.pdf [PubMed]
  • US Surgeon General. The health consequences of smoking. A report of the Surgeon General. Atlanta, Georgia: US Department of Health and Human Services, Centers for Disease Control and Prevention, National Center for Chronic Disease Prevention and Health Promotion, Office on Smoking and Health; 2004. http://www.cdc.gov/tobacco/data_statistics/sgr/2004/
  • Lee PN. Circulatory disease and smokeless tobacco in Western populations: a review of the evidence. Int J Epidemiol. 2007;36:789–804. doi: 10.1093/ije/dym039. [PubMed] [Cross Ref]
  • Thornton AJ, Lee PN. The relationship between European and American smokeless tobacco and diseases other than oral and cardiovascular. 2007. http://www.pnlee.co.uk/reflist.htm Download THORNT2007.pdf.
  • Hsing AW, McLaughlin JK, Schuman LM, Bjelke E, Gridley G, Wacholder S, Chien HTC. Diet, tobacco use and fatal prostate cancer: Results from the Lutheran brotherhood cohort study. Cancer Res. 1990;50:6836–6840. [PubMed]
  • Kneller RW, McLaughlin JK, Bjelke E, Schuman LM, Blot WJ, Wacholder S, Gridley G, CoChien HT, Fraumeni JF Jr. A cohort study of stomach cancer in a high-risk American population. Cancer. 1991;68:672–678. doi: 10.1002/1097-0142(19910801)68:3<672::AID-CNCR2820680339>3.0.CO;2-T. [PubMed] [Cross Ref]
  • Zheng W, McLaughlin JK, Gridley G, Bjelke E, Schuman LM, Silverman DT, Wacholder S, Co-Chien HT, Blot WJ, Fraumeni JF Jr. A cohort study of smoking, alcohol consumption, and dietary factors for pancreatic cancer (United States) Cancer Causes Control. 1993;4:477–482. doi: 10.1007/BF00050867. [PubMed] [Cross Ref]
  • International Agency for Research on Cancer. Tobacco habits other than smoking; betel-quid and areca-nut chewing; and some related nitrosamines. [IARC Monographs on the evaluation of the carcinogenic risk of chemicals to humans.] Vol. 37. Lyon, France: IARC; 1985. [PubMed]
  • Hsing AW, McLaughlin JK, Hrubec Z, Blot WJ, Fraumeni JF Jr. Tobacco use and prostate cancer: 26 year follow-up of US veterans. Am J Epidemiol. 1991;133:437–441. [PubMed]
  • Heineman EF, Zahm SH, McLaughlin JK, Vaught JB, Hrubec Z. A prospective study of tobacco use and multiple myeloma: evidence against an association. Cancer Causes Control. 1992;3:31–36. doi: 10.1007/BF00051909. [PubMed] [Cross Ref]
  • Zahm SH, Heineman EF, Vaught JB. Soft tissue sarcoma and tobacco use: data from a prospective cohort study of United States veterans. Cancer Causes Control. 1992;3:371–376. doi: 10.1007/BF00146891. [PubMed] [Cross Ref]
  • Heineman EF, Zahm SH, McLaughlin JK, Vaught JB. Increased risk of colorectal cancer among smokers: results of a 26-year follow-up of US veterans and a review. Int J Cancer. 1995;59:728–738. doi: 10.1002/ijc.2910590603. [PubMed] [Cross Ref]
  • Winn D, Walrath J, Blot W, Rogot E. Chewing tobacco and snuff in relation to cause of death in a large prospective cohort [Abstract] Am J Epidemiol. 1982;116:567.
  • Putnam SD, Cerhan JR, Parker AS, Bianchi GD, Wallace RB, Cantor KP, Lynch CF. Lifestyle and anthropometric risk factors for prostate cancer in a cohort of Iowa men. Ann Epidemiol. 2000;10:361–369. doi: 10.1016/S1047-2797(00)00057-0. [PubMed] [Cross Ref]
  • Accortt NA, Waterbor JW, Beall C, Howard G. Chronic disease mortality in a cohort of smokeless tobacco users. Am J Epidemiol. 2002;156:730–737. doi: 10.1093/aje/kwf106. [PubMed] [Cross Ref]
  • Accortt NA, Waterbor JW, Beall C, Howard G. Cancer incidence among a cohort of smokeless tobacco users (United States) Cancer Causes Control. 2005;16:1107–1115. doi: 10.1007/s10552-005-0247-0. [PubMed] [Cross Ref]
  • Henley SJ, Thun MJ, Connell C, Calle EE. Two large prospective studies of mortality among men who use snuff or chewing tobacco (United States) Cancer Causes Control. 2005;16:347–358. doi: 10.1007/s10552-004-5519-6. [PubMed] [Cross Ref]
  • Chao A, Thun MJ, Henley SJ, Jacobs EJ, McCullough ML, Calle EE. Cigarette smoking, use of other tobacco products and stomach cancer mortality in US adults: The Cancer Prevention Study II. Int J Cancer. 2002;101:380–389. doi: 10.1002/ijc.10614. [PubMed] [Cross Ref]
  • Henley SJ, Connell CJ, Richter P, Husten C, Pechacek T, Calle EE, Thun MJ. Tobacco-related disease mortality among men who switched from cigarettes to spit tobacco. Tob Control. 2007;16:22–28. doi: 10.1136/tc.2006.018069. [PMC free article] [PubMed] [Cross Ref]
  • Boffetta P, Aagnes B, Weiderpass E, Andersen A. Smokeless tobacco use and risk of cancer of the pancreas and other organs. Int J Cancer. 2005;114:992–995. doi: 10.1002/ijc.20811. [PubMed] [Cross Ref]
  • Heuch I, Kvåle G, Jacobsen BK, Bjelke E. Use of alcohol, tobacco and coffee, and risk of pancreatic cancer. Br J Cancer. 1983;48:637–643. [PMC free article] [PubMed]
  • Bolinder G, Alfredsson L, Englund A, de Faire U. Smokeless tobacco use and increased cardiovascular mortality among Swedish construction workers. Am J Public Health. 1994;84:399–404. doi: 10.2105/AJPH.84.3.399. [PMC free article] [PubMed] [Cross Ref]
  • Odenbro Å, Bellocco R, Boffetta P, Lindelöf B, Adami J. Tobacco smoking, snuff dipping and the risk of cutaneous squamous cell carcinoma: a nationwide cohort study in Sweden. Br J Cancer. 2005;92:1326–1328. doi: 10.1038/sj.bjc.6602475. [PMC free article] [PubMed] [Cross Ref]
  • Fernberg P, Odenbro A, Bellocco R, Boffetta P, Yudi Pawitan Y, Adami J. Tobacco use, body mass index and the risk of malignant lymphomas: a nationwide cohort study in Sweden. Int J Cancer. 2006;118:2298–2302. doi: 10.1002/ijc.21617. [PubMed] [Cross Ref]
  • Fernberg P, Odenbro A, Bellocco R, Boffetta P, Pawitan Y, Zendehdel K, Adami J. Tobacco use, body mass index, and the risk of leukemia and multiple myeloma: a nationwide cohort study in Sweden. Cancer Res. 2007;67:5983–5986. doi: 10.1158/0008-5472.CAN-07-0274. [PubMed] [Cross Ref]
  • Luo J, Ye W, Zendehdel K, Adami J, Adami H-O, Boffetta P, Nyrén O. Oral use of Swedish moist snuff (snus) and risk of cancer of the mouth, lung, and pancreas in male construction workers: a retrospective cohort study. Lancet. 2007;369:2015–2020. doi: 10.1016/S0140-6736(07)60678-3. [PubMed] [Cross Ref]
  • Odenbro Å, Gillgren P, Bellocco R, Boffetta P, Håkansson N, Adami J. The risk for cutaneous malignant melanoma, melanoma in situ and intraocular malignant melanoma in relation to tobacco use and body mass index. Br J Dermatol. 2007;156:99–105. doi: 10.1111/j.1365-2133.2006.07537.x. [PubMed] [Cross Ref]
  • Zendehdel K, Nyrén O, Luo J, Dickman PW, Boffetta P, Englund A, Ye W. Risk of gastroesophageal cancer among smokers and users of Scandinavian moist snuff. Int J Cancer. 2008;122:1095–1099. doi: 10.1002/ijc.23076. [PubMed] [Cross Ref]
  • Roosaar A, Johansson AL, Sandborgh-Englund G, Axéll T, Nyrén O. Cancer and mortality among users and nonusers of snus. Int J Cancer. 2008;123:168–173. doi: 10.1002/ijc.23469. [PubMed] [Cross Ref]
  • Vogler WR, Lloyd JW, Milmore BK. A retrospective study of etiological factors in cancer of the mouth, pharynx, and larynx. Cancer. 1962;15:246–258. doi: 10.1002/1097-0142(196203/04)15:2<246::AID-CNCR2820150206>3.0.CO;2-5. [PubMed] [Cross Ref]
  • Broders AC. Squamous-cell epithelioma of the lip. A study of five hundred and thirty-seven cases. JAMA. 1920;74:656–664. http://jama.ama-assn.org/content/vol74/issue10/index.dtl
  • Doll R, Hill AB. A study of the aetiology of carcinoma of the lung. Br Med J. 1952;2:1271–1286. doi: 10.1136/bmj.2.4797.1271. [PMC free article] [PubMed] [Cross Ref]
  • Moore GE, Bissinger LL, Proehl EC. Intraoral cancer and the use of chewing tobacco. J Am Geriatr Soc. 1953;1:497–506. [PubMed]
  • Wynder EL, Hultberg S, Jacobsson F, Bross IJ. Environmental factors in cancer of the upper alimentary tract. A Swedish study with special reference to Plummer-Vinson (Paterson-Kelly) syndrome. Cancer. 1957;10:470–487. doi: 10.1002/1097-0142(195705/06)10:3<470::AID-CNCR2820100309>3.0.CO;2-7. [PubMed] [Cross Ref]
  • Wynder EL, Bross IJ. Aetiological factors in mouth cancer: an approach to its prevention. Br Med J. 1957;May 18:1137–1143. doi: 10.1136/bmj.1.5028.1137. [PMC free article] [PubMed] [Cross Ref]
  • Peacock EE Jr, Greenberg BG, Brawley BW. The effect of snuff and tobacco on the production of oral carcinoma: An experimental and epidemiological study. Ann Surg. 1960;151:542–550. doi: 10.1097/00000658-196004000-00014. [PMC free article] [PubMed] [Cross Ref]
  • Lockwood K. On the etiology of bladder tumors in København-Frederiksberg: an inquiry of 369 patients and 369 controls. Acta Pathol Microbiol Scand. 1961;51(Suppl 145):1–166. [PubMed]
  • Wynder EL, Bross IJ. A study of etiological factors in cancer of the oesophagus. Cancer. 1961;14:389–413. doi: 10.1002/1097-0142(196103/04)14:2<389::AID-CNCR2820140220>3.0.CO;2-E. [PubMed] [Cross Ref]
  • Vincent RG, Marchetta F. The relationship of the use of tobacco and alcohol to cancer of the oral cavity, pharynx or larynx. Am J Surg. 1963;106:501–505. doi: 10.1016/0002-9610(63)90137-5. [PubMed] [Cross Ref]
  • Wynder EL, Onderdonk J, Mantel N. An epidemiological investigation of cancer of the bladder. Cancer. 1963;16:1388–1407. doi: 10.1002/1097-0142(196311)16:11<1388::AID-CNCR2820161104>3.0.CO;2-8. [PubMed] [Cross Ref]
  • Bennington JL, Laubscher FA. Epidemiologic studies on carcinoma of the kidney. I. Association of renal adenocarcinoma with smoking. Cancer. 1968;21:1069–1071. doi: 10.1002/1097-0142(196806)21:6<1069::AID-CNCR2820210607>3.0.CO;2-J. [PubMed] [Cross Ref]
  • Dunham LJ, Rabson SA, Stewart HL, Frank AS, Young JL Jr. Rates, interview, and pathology study of cancer of the urinary bladder in New Orleans, Louisiana. J Natl Cancer Inst. 1968;41:683–709. [PubMed]
  • Martínez I. Factors associated with cancer of the esophagus, mouth, and pharynx in Puerto Rico. J Natl Cancer Inst. 1969;42:1069–1094. [PubMed]
  • Keller AZ. Cellular types, survival, race, nativity, occupations, habits and associated diseases in the pathogenesis of lip cancers. Am J Epidemiol. 1970;91:486–499. [PubMed]
  • Cole P, Monson RR, Haning H, Friedell GH. Smoking and cancer of the lower urinary tract. N Engl J Med. 1971;284:129–134. [PubMed]
  • Bjelke EO. Epidemiologic studies of cancer of the stomach, colon, and rectum; with special emphasis on the role of diet. Diss Abstr Int. 1974;34/08–3:266–272.
  • Armstrong B, Garrod A, Doll R. A retrospective study of renal cancer with special reference to coffee and animal protein consumption. Br J Cancer. 1976;33:127–136. [PMC free article] [PubMed]
  • Browne RM, Camsey MC, Waterhouse JAH, Manning GL. Etiological factors in oral squamous cell carcinoma. Community Dent Oral Epidemiol. 1977;5:301–306. doi: 10.1111/j.1600-0528.1977.tb01018.x. [PubMed] [Cross Ref]
  • Williams RR, Horm JW. Association of cancer sites with tobacco and alcohol consumption and socioeconomic status of patients: interview study from the Third National Cancer Survey. J Natl Cancer Inst. 1977;58:525–547. [PubMed]
  • Wynder EL, Stellman SD. Comparative epidemiology of tobacco-related cancers. Cancer Res. 1977;37:4608–4622. [PubMed]
  • Engzell U, Englund A, Westerholm P. Nasal cancer associated with occupational exposure to organic dust. Acta Otolaryngol. 1978;86:437–442. [PubMed]
  • Howe GR, Burch JD, Miller AB, Cook GM, Esteve J, Morrison B, Gordon P, Chambers LW, Fodor G, Winsor GM. Tobacco use, occupation, coffee, various nutrients, and bladder cancer. J Natl Cancer Inst. 1980;64:701–713. [PubMed]
  • Westbrook KC, Suen JY, Hawkins JM, McKinney DC. In: Prevention and Detection of Cancer. Nieburg HE, editor. New York: Marcel Dekker; 1980. Snuff dipper's carcinoma: Fact or fiction? pp. 1367–1371.
  • Pottern LM, Morris LE, Blot WJ, Ziegler RG, Fraumeni JF Jr. Esophageal cancer among black men in Washington DC. I. Alcohol, tobacco and other risk factors. J Natl Cancer Inst. 1981;67:777–783. [PubMed]
  • Winn DM, Blot WJ, Shy CM, Pickle LW, Toledo A, Fraumeni JF Jr. Snuff dipping and oral cancer among women in the southern United States. N Engl J Med. 1981;304:745–749. [PubMed]
  • Mommsen S, Aagaard J. Tobacco as a risk factor in bladder cancer. Carcinogenesis. 1983;4:335–338. doi: 10.1093/carcin/4.3.335. [PubMed] [Cross Ref]
  • Wynder EL, Kabat G, Rosenberg S, Levenstein M. Oral cancer and mouthwash use. J Natl Cancer Inst. 1983;70:255–260. [PubMed]
  • Brinton LA, Blot WJ, Becker JA, Winn DM, Patterson Browder J, Farmer JC Jr, Fraumeni JF Jr. A case-control study of cancers of the nasal cavity and paranasal sinuses. Am J Epidemiol. 1984;119:896–906. [PubMed]
  • McLaughlin JK, Mandel JS, Blot WJ, Schuman LM, Mehl ES, Fraumeni JF Jr. A population-based case-control study of renal cell carcinoma. J Natl Cancer Inst. 1984;72:275–284. [PubMed]
  • Hartge P, Hoover R, Kantor A. Bladder cancer risk and pipes, cigars and smokeless tobacco. Cancer. 1985;55:901–906. doi: 10.1002/1097-0142(19850215)55:4<901::AID-CNCR2820550432>3.0.CO;2-Q. [PubMed] [Cross Ref]
  • Weinberg GB, Kuller LH, Stehr PA. A case-control study of stomach cancer in a coal mining region of Pennsylvania. Cancer. 1985;56:703–713. doi: 10.1002/1097-0142(19850801)56:3<703::AID-CNCR2820560344>3.0.CO;2-K. [PubMed] [Cross Ref]
  • Goodman MT, Morgenstern H, Wynder EL. A case-control study of factors affecting the development of renal cell cancer. Am J Epidemiol. 1986;124:926–941. [PubMed]
  • Kabat GC, Dieck GS, Wynder EL. Bladder cancer in nonsmokers. Cancer. 1986;57:362–367. doi: 10.1002/1097-0142(19860115)57:2<362::AID-CNCR2820570229>3.0.CO;2-F. [PubMed] [Cross Ref]
  • Stockwell HG, Lyman GH. Impact of smoking and smokeless tobacco on the risk of cancer of the head and neck. Head Neck Surg. 1986;9:104–110. doi: 10.1002/hed.2890090206. [PubMed] [Cross Ref]
  • Young TB, Ford CN, Brandenburg JH. An epidemiologic study of oral cancer in a statewide network. Am J Otolaryngol. 1986;7:200–208. doi: 10.1016/S0196-0709(86)80007-2. [PubMed] [Cross Ref]
  • Lindquist R, Nilsson B, Eklund G, Gahrton G. Increased risk of developing acute leukemia after employment as a painter. Cancer. 1987;60:1378–1384. doi: 10.1002/1097-0142(19870915)60:6<1378::AID-CNCR2820600636>3.0.CO;2-D. [PubMed] [Cross Ref]
  • Asal NR, Risser DR, Kadamani S, Geyer JR, Lee ET, Cherng N. Risk factors in renal cell carcinoma: I. Methodology, demographics, tobacco, beverage use, and obesity. Cancer Detect Prev. 1988;11:359–377. [PubMed]
  • Blot WJ, McLaughlin JK, Winn DM, Austin DF, Greenberg RS, Preston-Martin S, Bernstein L, Schoenberg JB, Stemhagen A, Fraumeni JF Jr. Smoking and drinking in relation to oral and pharyngeal cancer. Cancer Res. 1988;48:3282–3287. [PubMed]
  • Falk RT, Pickle LW, Fontham ET, Correa P, Fraumeni JF Jr. Life-style risk factors for pancreatic cancer in Louisiana: a case-control study. Am J Epidemiol. 1988;128:324–336. [PubMed]
  • Morris Brown L, Blot WJ, Schuman SH, Smith VM, Ershow AG, Marks RD, Fraumeni JF Jr. Environmental factors and high risk of esophageal cancer among men in coastal South Carolina. J Natl Cancer Inst. 1988;80:1620–1625. doi: 10.1093/jnci/80.20.1620. [PubMed] [Cross Ref]
  • Slattery ML, Schumacher MC, West DW, Robison LM. Smoking and bladder cancer: the modifying effect of cigarettes on other factors. Cancer. 1988;61:402–408. doi: 10.1002/1097-0142(19880115)61:2<402::AID-CNCR2820610233>3.0.CO;2-U. [PubMed] [Cross Ref]
  • Spitz MR, Fueger JJ, Goepfert H, Hong WK, Newell GR. Squamous cell carcinoma of the upper aerodigestive tract: a case comparison analysis. Cancer. 1988;61:203–208. doi: 10.1002/1097-0142(19880101)61:1<203::AID-CNCR2820610134>3.0.CO;2-6. [PubMed] [Cross Ref]
  • Burch JD, Rohan TE, Howe GR, Risch HA, Hill GB, Steele R, Miller AB. Risk of bladder cancer by source and type of tobacco exposure: a case-control study. Int J Cancer. 1989;44:622–628. doi: 10.1002/ijc.2910440411. [PubMed] [Cross Ref]
  • Franco EL, Kowalski LP, Oliveira BV, Curado MP, Pereira RN, Silva ME, Fava AS, Torloni H. Risk factors for oral cancer in Brazil: A case-control study. Int J Cancer. 1989;43:992–1000. doi: 10.1002/ijc.2910430607. [PubMed] [Cross Ref]
  • Hoar Zahm S, Blair A, Holmes FF, Boysen CD, Robel RJ, Fraumeni JF Jr. A case-control study of soft-tissue sarcoma. Am J Epidemiol. 1989;130:665–674. [PubMed]
  • Farrow DC, Davis S. Risk of pancreatic cancer in relation to medical history and the use of tobacco, alcohol and coffee. Int J Cancer. 1990;45:816–820. doi: 10.1002/ijc.2910450504. [PubMed] [Cross Ref]
  • Blomqvist G, Hirsch J-M, Alberius P. Association between development of lower lip cancer and tobacco habits. J Oral Maxillofac Surg. 1991;49:1044–1047. doi: 10.1016/0278-2391(91)90134-8. [PubMed] [Cross Ref]
  • Ghadirian P, Simard A, Baillargeon J. Tobacco, alcohol and coffee and cancer of the pancreas. Cancer. 1991;67:2664–2670. doi: 10.1002/1097-0142(19910515)67:10<2664::AID-CNCR2820671043>3.0.CO;2-K. [PubMed] [Cross Ref]
  • Maden C, Beckmann AM, Thomas DB, McKnight B, Sherman KJ, Ashley RL, Corey L, Daling JR. Human papillomaviruses, herpes simplex viruses, and the risk of oral cancer in men. Am J Epidemiol. 1992;135:1093–1102. [PubMed]
  • Marshall JR, Graham S, Haughey BP, Shedd D, O'Shea R, Brasure J, Wilkinson GS, West D. Smoking, alcohol, dentition and diet in the epidemiology of oral cancer. Eur J Cancer B Oral Oncol. 1992;28B:9–15. doi: 10.1016/0964-1955(92)90005-L. [PubMed] [Cross Ref]
  • Morris Brown L, Gibson R, Blair A, Burmeister LF, Schuman LM, Cantor KP, Fraumeni JF Jr. Smoking and risk of leukemia. Am J Epidemiol. 1992;135:763–768. [PubMed]
  • Morris Brown L, Everett GD, Gibson R, Burmeister LF, Schuman LM, Blair A. Smoking and risk of non-Hodgkin's lymphoma and multiple myeloma. Cancer Causes Control. 1992;3:49–55. doi: 10.1007/BF00051912. [PubMed] [Cross Ref]
  • Sterling TD, Rosenbaum WL, Weinkam JJ. Analysis of the relationship between smokeless tobacco and cancer based on data from the national mortality followback survey. J Clin Epidemiol. 1992;45:223–231. doi: 10.1016/0895-4356(92)90082-X. [PubMed] [Cross Ref]
  • Mashberg A, Boffetta P, Winkelman R, Garfinkel L. Tobacco smoking, alcohol drinking, and cancer of the oral cavity and oropharynx among U.S. veterans. Cancer. 1993;72:1369–1375. doi: 10.1002/1097-0142(19930815)72:4<1369::AID-CNCR2820720436>3.0.CO;2-L. [PubMed] [Cross Ref]
  • Gross AJ, Lackland DT, Tu DS. Oral cancer and smokeless tobacco: literature review and meta-analysis. Environ Int. 1995;21:381–394. doi: 10.1016/0160-4120(95)00040-R. [Cross Ref]
  • Spitz MR, Fueger JJ, Halabi S, Schantz SP, Sample D, Hsu TC. Mutagen sensitivity in upper aerodigestive tract cancer: a case-control analysis. Cancer Epidemiol Biomarkers Prev. 1993;2:329–333. [PubMed]
  • Chow W-H, McLaughlin JK, Menck HR, Mack TM. Risk factors for extrahepatic bile duct cancers: Los Angeles County, California (USA) Cancer Causes Control. 1994;5:267–272. doi: 10.1007/BF01830247. [PubMed] [Cross Ref]
  • Hansson L-E, Baron J, Nyrén O, Bergström R, Wolk A, Adami H-O. Tobacco, alcohol and the risk of gastric cancer. A population-based case-control study in Sweden. Int J Cancer. 1994;57:26–31. doi: 10.1002/ijc.2910570106. [PubMed] [Cross Ref]
  • Hardell L, Eriksson M, Degerman A. Exposure to phenoxyacetic acids, chlorophenols, or organic solvents in relation to histopathology, stage, and anatomical localization of non-Hodgkin's lymphoma. Cancer Res. 1994;54:2386–2389. [PubMed]
  • Hayes RB, Pottern LM, Swanson GM, Liff JM, Schoenberg JB, Greenberg RS, Schwartz AG, Brown LM, Silverman DT, Hoover RN. Tobacco use and prostate cancer in Blacks and Whites in the United States. Cancer Causes Control. 1994;5:221–226. doi: 10.1007/BF01830240. [PubMed] [Cross Ref]
  • Kabat GC, Chang CJ, Wynder EL. The role of tobacco, alcohol use, and body mass index in oral and pharyngeal cancer. Int J Epidemiol. 1994;23:1137–1144. doi: 10.1093/ije/23.6.1137. [PubMed] [Cross Ref]
  • Bundgaard T, Wildt J, Frydenberg M, Elbrønd O, Nielsen JE. Case-control study of squamous cell cancer of the oral cavity in Denmark. Cancer Causes Control. 1995;6:57–67. doi: 10.1007/BF00051681. [PubMed] [Cross Ref]
  • McLaughlin JK, Lindblad P, Mellemgaard A, McCredie M, Mandel JS, Schlehofer B, Pommer W, Adami H-O. International Renal-cell Cancer Study. I. Tobacco use. Int J Cancer. 1995;60:194–198. doi: 10.1002/ijc.2910600211. [PubMed] [Cross Ref]
  • Muscat JE, Hoffmann D, Wynder EL. The epidemiology of renal cell carcinoma. A second look. Cancer. 1995;75:2552–2557. doi: 10.1002/1097-0142(19950515)75:10<2552::AID-CNCR2820751023>3.0.CO;2-1. [PubMed] [Cross Ref]
  • Muscat JE, Stellman SD, Hoffmann D, Wynder EL. Smoking and pancreatic cancer in men and women. Cancer Epidemiol Biomarkers Prev. 1997;6:15–19. [PubMed]
  • Lewin F, Norell SE, Johansson H, Gustavsson P, Wennerberg J, Biörklund A, Rutqvist LE. Smoking tobacco, oral snuff, and alcohol in the etiology of squamous cell carcinoma of the head and neck: a population-based case-referent study in Sweden. Cancer. 1998;82:1367–1375. doi: 10.1002/(SICI)1097-0142(19980401)82:7<1367::AID-CNCR21>3.0.CO;2-3. [PubMed] [Cross Ref]
  • Muscat JE, Wynder EL. A case/control study of risk factors for major salivary gland cancer. Otolaryngol Head Neck Surg. 1998;118:195–198. doi: 10.1016/S0194-5998(98)80013-2. [PubMed] [Cross Ref]
  • Schildt E-B, Eriksson M, Hardell L, Magnuson A. Oral snuff, smoking habits and alcohol consumption in relation to oral cancer in a Swedish case-control study. Int J Cancer. 1998;77:341–346. doi: 10.1002/(SICI)1097-0215(19980729)77:3<341::AID-IJC6>3.0.CO;2-O. [PubMed] [Cross Ref]
  • Schwartz SM, Daling JR, Doody DR, Wipf GC, Carter JJ, Madeleine MM, Mao E-J, Fitzgibbons ED, Huang S, Beckmann AM, McDougall JK, Galloway DA. Oral cancer risk in relation to sexual history and evidence of human papillomavirus infection. J Natl Cancer Inst. 1998;90:1626–1636. doi: 10.1093/jnci/90.21.1626. [PubMed] [Cross Ref]
  • Yuan J-M, Esteban Castelao J, Gago-Dominguez M, Yu MC, Ross RK. Tobacco use in relation to renal cell carcinoma. Cancer Epidemiol Biomarkers Prev. 1998;7:429–433. [PubMed]
  • Ye W, Ekström AM, Hansson L-E, Bergström R, Nyrén O. Tobacco, alcohol and the risk of gastric cancer by sub-site and histologic type. Int J Cancer. 1999;83:223–229. doi: 10.1002/(SICI)1097-0215(19991008)83:2<223::AID-IJC13>3.0.CO;2-M. [PubMed] [Cross Ref]
  • Lagergren J, Bergström R, Lindgren A, Nyrén O. The role of tobacco, snuff and alcohol use in the aetiology of cancer of the oesophagus and gastric cardia. Int J Cancer. 2000;85:340–346. doi: 10.1002/(SICI)1097-0215(20000201)85:3<340::AID-IJC8>3.0.CO;2-N. [PubMed] [Cross Ref]
  • Zheng T, Cantor KP, Zhang Y, Chiu BCH, Lynch CF. Risk of brain glioma not associated with cigarette smoking or use of other tobacco products in Iowa. Cancer Epidemiol Biomarkers Prev. 2001;10:413–414. [PubMed]
  • Schroeder JC, Olshan AF, Baric R, Dent GA, Weinberg CR, Yount B, Cerhan JR, Lynch CF, Schuman LM, Tolbert PE, Rothman N, Cantor KP, Blair A. A case-control study of tobacco use and other non-occupational risk factors for t(14;18) subtypes of non-Hodgkin's lymphoma (United States) Cancer Causes Control. 2002;13:159–168. doi: 10.1023/A:1014397920185. [PubMed] [Cross Ref]
  • Alguacil J, Silverman DT. Smokeless and other noncigarette tobacco use and pancreatic cancer: a case-control study based on direct interviews. Cancer Epidemiol Biomarkers Prev. 2004;13:55–58. doi: 10.1158/1055-9965.EPI-03-0033. [PubMed] [Cross Ref]
  • Bracci PM, Holly EA. Tobacco use and non-Hodgkin lymphoma: results from a population-based case-control study in the San Francisco Bay Area, California. Cancer Causes Control. 2005;16:333–346. doi: 10.1007/s10552-004-4324-6. [PubMed] [Cross Ref]
  • Rosenquist K, Wennerberg J, Schildt E-B, Bladström A, Hansson BG, Andersson G. Use of Swedish moist snuff, smoking and alcohol consumption in the aetiology of oral and oropharyngeal squamous cell carcinoma. A population-based case-control study in southern Sweden. Acta Otolaryngol. 2005;125:991–998. doi: 10.1080/00016480510043440. [PubMed] [Cross Ref]
  • Hassan MM, Abbruzzese JL, Bondy ML, Wolff RA, Vauthey J-N, Pisters PW, Evans DB, Khan R, Lenzi R, Jiao L, Li D. Passive smoking and the use of noncigarette tobacco products in association with risk for pancreatic cancer: a case-control study. Cancer. 2007;109:2547–2556. doi: 10.1002/cncr.22724. [PMC free article] [PubMed] [Cross Ref]
  • Breslow NE, Day NE. In: The analysis of case-control studies. [Statistical methods in cancer research.] Davis W, editor. Vol. 1. Lyon: IARC; IARC Scientific Publication No. 32; 1980. [PubMed]
  • Fleiss JL, Gross AJ. Meta-analysis in epidemiology, with special reference to studies of the association between exposure to environmental tobacco smoke and lung cancer: a critique. J Clin Epidemiol. 1991;44:127–139. doi: 10.1016/0895-4356(91)90261-7. [PubMed] [Cross Ref]
  • Greenland S, Longnecker MP. Methods for trend estimation from summarized dose-response data, with applications to meta-analysis. Am J Epidemiol. 1992;135:1301–1309. [PubMed]
  • Hamling J, Lee P, Weitkunat R, Ambühl M. Facilitating meta-analyses by deriving relative effect and precision estimates for alternative comparisons from a set of estimates presented by exposure level or disease category. Stat Med. 2008;27:954–970. doi: 10.1002/sim.3013. [PubMed] [Cross Ref]
  • Armitage P, Berry G. Statistical methods in medical research. 3. Oxford: Blackwell Publishing; 1994.
  • Higgins JPT, Thompson SG, Deeks JJ, Altman DG. Measuring inconsistency in meta-analyses. BMJ. 2003;327:557–560. doi: 10.1136/bmj.327.7414.557. [PMC free article] [PubMed] [Cross Ref]
  • Egger M, Davey Smith G, Schneider M, Minder C. Bias in meta-analysis detected by a simple, graphical test. BMJ. 1997;315:629–634. [PMC free article] [PubMed]
  • US Surgeon General. Reducing the health consequences of smoking. 25 years of progress. A report of the Surgeon General. Rockville, Maryland: US Department of Health and Human Services; Public Health Services; DHHS Publication No. (CDC) 89-8411; 1989. http://profiles.nlm.nih.gov/NN/B/B/X/S/
  • World Health Organization. WHO Mortality Database. http://www3.who.int/whosis
  • Inter-University Consortium for Political and Social Research (ICPSR) National Health Interview Survey, 2005. ICPSR Study No. 4606. Online analysis. U.S. Department of Health and Human Services, National Center for Health Statistics; http://www.icpsr.umich.edu/cocoon/ICPSR/DAS/04606.xml (Accessed October 2008).
  • Spangler JG, Michielutte R, Bell RA, Dignan MB. Association between smokeless tobacco use and breast cancer among Native-American women in North Carolina. Ethn Dis. 2001;11:36–43. [PubMed]
  • Spangler JG, Michielutte R, Bell RA, Dignan MB. Correction to: Association between smokeless tobacco use and breast cancer among native-American women in North Carolina (Ethn.Dis.2001;11:36–43) Ethn Dis. 2002;12:158–159. [PubMed]
  • World Health Organization. International statistical classification of diseases and related health problems. Tenth revision. Vol. 1. Geneva: WHO; 1992.
  • Nilsson R. De minimus non curat lex – virtual thresholds for cancer initiation by tobacco specific nitrosamines – prospects for harm reduction by smokeless tobacco. Int J Occup Environ Health. 2006;19:1–30. doi: 10.2478/v10001-006-0011-z. http://versita.metapress.com/content/r3155663g2025g8t/fulltext.pdf [PubMed] [Cross Ref]
  • Peto R, Lopez AD, Boreham J, Thun M, Heath C. , Jr. Mortality from smoking in developed countries 1950–2000. Indirect estimates from national vital statistics. Oxford, New York, Tokyo: Oxford University Press; 1994.

Articles from BMC Medicine are provided here courtesy of BioMed Central
PubReader format: click here to try


Save items

Related citations in PubMed

See reviews...See all...

Cited by other articles in PMC

See all...


  • Cited in Books
    Cited in Books
    NCBI Bookshelf books that cite the current articles.
  • Compound
    PubChem chemical compound records that cite the current articles. These references are taken from those provided on submitted PubChem chemical substance records. Multiple substance records may contribute to the PubChem compound record.
  • MedGen
    Related information in MedGen
  • PubMed
    PubMed citations for these articles
  • Substance
    PubChem chemical substance records that cite the current articles. These references are taken from those provided on submitted PubChem chemical substance records.

Recent Activity

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...