Evaluation of soy phytoestrogens for the treatment of hot flashes in breast cancer survivors: A North Central Cancer Treatment Group trial

被引:261
作者
Quella, SK
Loprinzi, CL
Barton, DL
Knost, JA
Sloan, JA
LaVasseur, BI
Swan, D
Krupp, KR
Miller, KD
Novotny, PJ
机构
[1] Mayo Clin & Mayo Fdn, Rochester, MN 55905 USA
[2] Duluth Community Clin Oncol Program, Duluth, MN USA
[3] Carle Canc Ctr, Community Clin Oncol Program, Urbana, IL USA
[4] Illinois Oncol Res Assoc, Community Clin Oncol Program, Peoria, IL USA
[5] Ann Arbor Reg Community Clin Oncol Program, Ann Arbor, MI USA
[6] Toledo Community Hosp, Oncol Program, Community Clin Oncol Program, Toledo, OH USA
[7] Meritcare Hosp, Community Clin Oncol Program, Fargo, ND USA
关键词
D O I
10.1200/JCO.2000.18.5.1068
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Hot flashes represent a significant clinical problem for some breast cancer survivors. Safe, effective treatment is needed for this prominent clinical problem. Although it has been shown that estrogen or progesterone replacement therapy can alleviate this problem, there are continued safety concerns regarding the use of hormonal therapies in these women. Based on anecdotal information, we hypothesized that soy-derived phytoestrogens, weak estrogen-like substances in the soybean that demonstrate estrogen agonist and/or antagonist effects when they bind to estrogen receptors, could alleviate hot flashes. This current trial was designed to investigate this hypothesis, Patients and Methods: This double-blind clinical trial involved breast cancer survivors with substantial hot flashes, After randomization, patients underwent a I-week baseline period with no therapy, This was followed by 4 weeks of either say tablets or placebo. The patients then crossed over to the opposite arm in a double-blind manner for the last 4 weeks. patients completed ct daily questionnaire documenting hot flash frequency, intensity, and perceived side effects. Results: Of the 177 women who were randomized and started the study substance, 155 (88%) provided useable data over the first 5 weeks; 149 provided usable data over the entire 9 weeks, There was no suggestion that the say product was more effective in reducing hot flashes than the placebo, At study completion, patients preferred the say product 33% of the time, the placebo 37% of the time, and neither substance 31% of the time. No toxicity was observed. Conclusion: The say product did not alleviate hot flashes in breast cancer survivors. J Clin Oncol 18:1068-1074, (C) 2000 by American Society of Clinical Oncology.
引用
收藏
页码:1068 / 1074
页数:7
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