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Cochrane Database of Systematic Reviews: Plain Language Summaries [Internet]. Chichester, UK: John Wiley & Sons, Ltd; 2003-. doi: 10.1002/14651858.CD008946.pub2

Cochrane Database of Systematic Reviews: Plain Language Summaries [Internet].

Treatments for mycosis fungoides (a malignant condition with blood cells initially affecting the skin)

This version published: 2016; Review content assessed as up-to-date: January 12, 2011.

Link to full article: [Cochrane Library]

Plain language summary

Mycosis fungoides is a chronic, malignant disease causing blood cells responsible for the human immune system to affect the skin. People of all ages and from all ethnic backgrounds can develop this disease. Mycosis fungoides can cause physical symptoms that typically occur in a certain sequence making it possible to classify the disease in different stages. Usually this disease starts with patches on the body and extremities. After some time (often years), these patches develop into plaques, and further progress into solid tumours is possible. Lymph nodes and other organs can also be affected, but progress of the disease in most cases is slow compared to other malignant diseases. Life expectancy in the first stage of the disease is similar to people without mycosis fungoides; whereas, prognosis in the later stages of the disease gets worse.

Several treatment options like local therapy with creams and ointments, localised injections of drugs, application of UV or radioactive radiation, or chemotherapy are used for treatment of this disease. They are not curative but try to ease symptoms like itching or burning of the patches or plaques.

We found 14 studies with a total of 30 publications with 675 participants. Most of the studies (8) had fewer than 50 participants and lasted less than 12 months. None of these studies compared the quality of life of participants with regard to different treatments. Also, no study compared a particular therapy to a "wait and see" strategy.

Most of the studies described adverse effects, from mild symptoms to severe life‐threatening or even lethal complications depending upon the type of treatment. More aggressive treatment options like systemic chemotherapy showed more adverse effects than topical therapies that are applied directly to the skin. None of the trials reported a long‐term benefit (i.e. clearance of all symptoms of disease lasting at least two years). Therefore, the conclusions from these studies should be treated with caution.

Treatment of mycosis fungoides should be based on the stage of progression of the disease with a focus on the limitations of severe adverse effects. There is a great need for extensive and well planned research to find effective ways to manage this disease and to evaluate treatment strategies that might be curative. People with mycosis fungoides are encouraged to participate in such trials.

Abstract

Background: Mycosis fungoides is the most common type of cutaneous T cell lymphoma, a malignant, chronic disease initially affecting the skin. Several therapies are available, which may induce clinical remission for a time.

Objectives: To assess the effects of interventions for mycosis fungoides in all stages of the disease.

Search methods: We searched the following databases up to January 2011: the Cochrane Skin Group Specialised Register, CENTRAL in The Cochrane Library, MEDLINE (from 2005), EMBASE (from 2010), and LILACS (from 1982). We also checked reference lists of included studies for further references to relevant RCTs. We searched online trials registries for further references to unpublished trials and undertook a separate search for adverse effects of interventions for mycosis fungoides in non‐RCTs in MEDLINE in May 2011.

Selection criteria: Randomised controlled trials (RCTs) of interventions for mycosis fungoides in people with any stage of the disease. At least 90% of participants in the trials must have been diagnosed with mycosis fungoides (Alibert‐Bazin‐type).

Data collection and analysis: Two authors independently assessed eligibility and methodological quality for each study and carried out data extraction. We resolved any disagreement by discussion. Primary outcomes were the impact on quality of life and the safety of interventions. When available, we reported on our secondary outcomes, which were the improvement or clearance of skin lesions, disease‐free intervals, survival rates, relapse rates, and rare adverse effects. When possible, we combined homogeneous studies for meta‐analysis. We used The Cochrane Collaboration's 'Risk of bias' tool to assess the internal validity of all included studies in six different domains.

Main results: The review included 14 RCTs involving 675 participants, covering a wide range of interventions. Eleven of the included trials assessed participants in clinical stages IA to IIB only.

Internal validity was considerably low in studies with a high or unclear risk of bias. The main reasons for this were low methodological quality or missing data, even after we contacted the study authors, and a mean dropout rate of 26% (0% to 72%). Study size was generally small with a minimum of 4 and a maximum of 103 participants. Only one study provided a long enough follow‐up for reliable survival analysis.

Included studies assessed topical treatments, such as imiquimod, peldesine, hypericin, nitrogen mustard, as well as intralesional injections of interferon‐α (IFN‐α). The light therapies investigated included psoralen plus ultraviolet A light (PUVA), extracorporeal photopheresis (photochemotherapy), and visible light. Oral treatments included acitretin, bexarotene, and methotrexate. Treatment with parenteral systemic agents consisted of denileukin diftitox; a combination of chemotherapy and electron beam radiation; and intramuscular injections of active transfer factor. Nine studies evaluated therapies by using an active comparator; five were placebo‐controlled RCTs.

Twelve studies reported on common adverse effects, while only two assessed quality of life. None of these studies compared the health‐related quality of life of participants undergoing different treatments. Most of the reported adverse effects were attributed to the interventions. Systemic treatments, and here in particular a combined therapeutic regimen of chemotherapy and electron beam, bexarotene, or denileukin diftitox, showed more adverse effects than topical or skin‐directed treatments.

In the included studies, clearance rates ranged from 0% to 83%, and improvement ranged from 0% to 88%. The meta‐analysis combining the results of 2 trials comparing the effect of IFN‐α and PUVA versus PUVA alone showed no significant difference in the relative risk of clearance: 1.07 (95% confidence interval 0.87 to 1.31). None of the included studies demonstrated a significant increase in disease‐free intervals, relapse, or overall survival.

Authors' conclusions: This review identified trial evidence for a range of different topical and systemic interventions for mycosis fungoides. Because of substantial heterogeneity in design, small sample sizes, and low methodological quality, the comparative safety and efficacy of these interventions cannot be established on the basis of the included RCTs. Taking into account the possible serious adverse effects and the limited availability of efficacy data, topical and skin‐directed treatments are recommended first, especially in the early stages of disease. More aggressive therapeutic regimens may show improvement or clearance of lesions, but they also result in more adverse effects; therefore, they are to be considered with caution. Larger studies with comparable, clearly‐defined end points for all stages of mycosis fungoides, and a focus on safety, quality of life, and duration of remission as part of the outcome measures, are necessary.

Editorial Group: Cochrane Skin Group.

Publication status: Edited (no change to conclusions).

Citation: Weberschock T, Strametz R, Lorenz M, Röllig C, Bunch C, Bauer A, Schmitt J. Interventions for mycosis fungoides. Cochrane Database of Systematic Reviews 2012, Issue 9. Art. No.: CD008946. DOI: 10.1002/14651858.CD008946.pub2. Link to Cochrane Library. [PubMed: 22972128]

Copyright © 2016 The Cochrane Collaboration. Published by John Wiley & Sons, Ltd.

PMID: 22972128

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