Efficacy of taxanes as adjuvant treatment of breast cancer: a review and meta-analysis of randomised clinical trials

被引:23
作者
Gines, Jordi [1 ]
Sabater, Eliazar [2 ]
Martorell, Clara [1 ]
Grau, Maria [2 ]
Monroy, Marta [1 ]
Casado, Miguel A. [2 ]
机构
[1] Hosp Univ Son Espases, Serv Farm, ES-07010 Palma De Mallorca, Baleares, Spain
[2] Pharmacoecon & Outcomes Res Iberia, Madrid, Spain
关键词
Taxanes; Docetaxel; Paclitaxel; Meta-analysis; Adjuvant treatment; Breast cancer; DOXORUBICIN PLUS CYCLOPHOSPHAMIDE; PHASE-III TRIAL; FOLLOW-UP; DOSE-DENSE; SURVIVAL BENEFIT; HIGH-RISK; CHEMOTHERAPY; PACLITAXEL; DOCETAXEL; EPIRUBICIN;
D O I
10.1007/s12094-011-0686-x
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
To evaluate the magnitude of benefit obtained by taxanes as adjuvant treatment of breast cancer and to assess the best method for their administration. We performed a systematic search of phase III randomised clinical trials that included patients with non-metastatic breast cancer in whom comparisons were chemotherapy (CT) containing a taxane (docetaxel or paclitaxel) vs. CT without taxanes (first-generation trials), or CT with taxane in both treatment arms (second-generation trials), administered after surgery. The parameters of efficacy evaluated were disease-free survival (DFS) and overall survival (OS). The data obtained in the first-generation trials (number of relapses and deaths) were submitted to a meta-analysis. The odds ratio (OR) combined with DerSimonian and Laird (OR DL) and 95% confidence interval (95%CI) were calculated. Further, an analysis was performed of those trials that included only patients with nodal involvement (N+). In both cases, the results were also analysed as a function of the taxane used, and with indirect comparisons between the two. The second-generation trials were analysed to assess the optimum method of administration. A total of 17 trials were selected for the metaanalysis (30,672 patients). The OR DL was 0.82 (95%CI: 0.76=2-0.88) for DFS and 0.83 (95%CI: 0.75-0.91) for OS. In N+ patients the results were 0.80 (95%CI: 0.74-0.86) and 0.79 (95%CI: 0.69-0.89), respectively. Docetaxel and paclitaxel significantly increased the DFS and OS. In our indirect comparison, the benefit of docetaxel on OS was significantly superior to that obtained with paclitaxel in N+ patients (OR: 0.79; 95%CI: 0.63-0.98). The administration of adjuvant CT-based taxanes reduces the risk of relapse and death. This reduction is superior in clinical trials that included only N+ patients. With the available evidence, it would appear that the best method of administering paclitaxel is weekly and for docetaxel tri-weekly.
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收藏
页码:485 / 498
页数:14
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