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Clin Cancer Res. 2015 Feb 1;21(3):514-25. doi: 10.1158/1078-0432.CCR-14-2544. Epub 2015 Jan 8.

Electronic nicotine delivery systems: a policy statement from the American Association for Cancer Research and the American Society of Clinical Oncology.

Author information

1
Moffitt Cancer Center, Tampa, Florida.
2
Roswell Park Cancer Institute, Buffalo, New York.
3
Indiana University Health Simon Cancer Center, Indianapolis, IN.
4
Masonic Cancer Center, Minneapolis, Minnesota.
5
Yale Comprehensive Cancer Center, New Haven, Connecticut. roy.herbst@yale.edu.
6
The American Association for Cancer Research, Philadelphia, Pennsylvania.
7
Memorial Sloan Kettering Cancer Center, New York, New York.
8
The Ohio State University Medical Center, Columbus, Ohio.
9
Yale Comprehensive Cancer Center, New Haven, Connecticut.
10
American Society of Clinical Oncology, Alexandria, Virginia.
11
Dana-Farber Cancer Institute, Boston, Massachusetts.
12
Medical University of South Carolina, Charleston, South Carolina.

Abstract

Combustible tobacco use remains the number one preventable cause of disease, disability, and death in the United States. Electronic nicotine delivery systems (ENDS), which include e-cigarettes, are devices capable of delivering nicotine in an aerosolized form. ENDS use by both adults and youth has increased rapidly, and some have advocated these products could serve as harm-reduction devices and smoking cessation aids. ENDS may be beneficial if they reduce smoking rates or prevent or reduce the known adverse health effects of smoking. However, ENDS may also be harmful, particularly to youth, if they increase the likelihood that nonsmokers or formers smokers will use combustible tobacco products or if they discourage smokers from quitting. The American Association for Cancer Research (AACR) and the American Society of Clinical Oncology (ASCO) recognize the potential ENDS have to alter patterns of tobacco use and affect the public's health; however, definitive data are lacking. AACR and ASCO recommend additional research on these devices, including assessing the health impacts of ENDS, understanding patterns of ENDS use, and determining what role ENDS have in cessation. Key policy recommendations include supporting federal, state, and local regulation of ENDS; requiring manufacturers to register with the FDA and report all product ingredients, requiring childproof caps on ENDS liquids, and including warning labels on products and their advertisements; prohibiting youth-oriented marketing and sales; prohibiting child-friendly ENDS flavors; and prohibiting ENDS use in places where cigarette smoking is prohibited.

PMID:
25573384
DOI:
10.1158/1078-0432.CCR-14-2544
[Indexed for MEDLINE]
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