A double-blind placebo-controlled randomized study of Chinese herbal medicine as complementary therapy for reduction of chemotherapy-induced toxicity

被引:62
作者
Mok, T. S. K. [1 ]
Yeo, W.
Johnson, P. J.
Hui, P.
Ho, W. M.
Lam, K. C.
Xu, M.
Chak, K.
Chan, A.
Wong, H.
Mo, F.
Zee, B.
机构
[1] Chinese Univ Hong Kong, Prince Wales Hosp, Inst Chinese Med, Hong Kong Canc Inst,Dept Clin Oncol, Shatin, Hong Kong, Peoples R China
[2] Univ Birmingham, Dept Oncol, Birmingham, W Midlands, England
[3] Baptist Hosp, Sch Chinese Med, Hong Kong, Hong Kong, Peoples R China
[4] Chinese Univ Hong Kong, Sch Publ Hlth, Ctr Clin Trials, Sha Tin 100083, Hong Kong, Peoples R China
关键词
alternative and complementary medicine; chemotherapy; Chinese herbal medicine; colonic neoplasms; emesis; toxicity;
D O I
10.1093/annonc/mdl465
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Background: Chinese herbal medicine (CHM) is a common complementary therapy used by patients with cancer for reduction of chemotherapy-induced toxic effects. This study applied the highest standard of clinical trial methodology to examine the role of CHM in reducing chemotherapy-induced toxicity, while maintaining a tailored approach to therapy. Patients and methods: Patients with early-stage breast or colon cancer who required postoperative adjuvant chemotherapy were eligible for the study. Enrolled patients were randomly assigned to one of three Chinese herbalists who evaluated and prescribed a combination of single-item packaged herbal extract granules. Patients received either CHM or placebo packages with a corresponding serial number. The placebo package contained nontherapeutic herbs with an artificial smell and taste similar to a typical herbal tea. The primary end points were hematologic and non-hematologic toxicity according to the National Cancer Institute Common Toxicity Criteria Version 2. Results: One hundred and twenty patients were accrued at the time of premature study termination. Patient characteristics of the two groups were similar. The incidence of grade 3/4 anemia, leukopenia, neutropenia, and thrombocytopenia for the CHM and placebo groups were 5.4%, 47.3%, 52.7%, and 1.8% and 1.8%, 32.2%, 44.7%, and 3.6%, respectively (P = 0.27, 0.37, 0.63, and 0.13, respectively). Incidence of grade 2 nausea was the only non-hematologic toxicity that was significantly reduced in the CHM group (14.6% versus 35.7%, P = 0.04). Conclusions: Traditional CHM does not reduce the hematologic toxicity associated with chemotherapy. CHM, however, does have a significant impact on control of nausea.
引用
收藏
页码:768 / 774
页数:7
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