Double-blind, placebo-controlled, randomized study of eicosapentaenoic acid diester in patients with cancer cachexia

被引:207
|
作者
Fearon, Kenneth C. H.
Barber, Matthew D.
Moses, Alastair G.
Ahmedzai, Sam H.
Taylor, Gillian S.
Tisdale, Michael J.
Murray, Gordon D.
机构
[1] Royal Infirm, Dept Clin & Surg Sci Surg, Edinburgh EH16 4SA, Midlothian, Scotland
[2] Univ Edinburgh, Sch Med, Edinburgh, Midlothian, Scotland
[3] Univ Sheffield, Royal Hallamshire Hosp, Acad Unit Support Care, Sheffield S10 2JF, S Yorkshire, England
[4] Aston Univ, Inst Pharmaceut Sci, CRC Nutr Biochem Res Grp, Birmingham B4 7ET, W Midlands, England
关键词
D O I
10.1200/JCO.2005.04.5724
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose Eicosapentaenoic acid (EPA) has been proposed to have specific anticachectic effects. This trial compared EPA diethyl ester with placebo in cachectic cancer patients for effects on weight and lean body mass. Patients and Methods Five hundred eighteen weight-losing patients with advanced gastrointestinal or lung cancer were studied in a multicenter, double-blind, placebo controlled trial. Patients were randomly assigned to receive a novel preparation of pure EPA at a dose of 2 g or 4 g daily or placebo (2g EPA, in = 175; 4 g EPA, n = 172; placebo, n = 171). Patients were assessed at 4 weeks and 8 weeks. Results The groups were well balanced at baseline. Mean weight loss at baseline was 18% (n = 518). Over the 8-week treatment period, both intention-to-treat analysis and per protocol analysis revealed no statistically significant improvements in survival, weight, or other nutritional variables. There was, however, a trend in favor of EPA with analysis of the primary end point, weight, at 8 weeks showing a borderline, nonsignificant treatment effect (P=.066). Relative to placebo, mean weight increased by 1.2 kg with 2 g EPA (95% Cl, 0 kg to 2.3 <g) and by 0.3 kg with 4g EPA (-0.9 kg to 1.5 kg). Conclusion The results indicate no statistically significant benefit from single agent EPA in the treatment of cancer cachexia. Future studies should concentrate on other agents or combination regimens.
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收藏
页码:3401 / 3407
页数:7
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