Estrogen receptor expression and efficacy of docetaxel-containing adjuvant chemotherapy in patients with node-positive breast cancer: Results from a pooled analysis

被引:47
作者
Andre, Fabrice
Broglio, Kristine
Roche, Henri
Martin, Miguel
Mackey, John R.
Penault-Llorca, Frederique
Hortobagyi, Gabriel N.
Pusztai, Lajos
机构
[1] Univ Texas Houston, MD Anderson Canc Ctr, Div Quantitat Sci, Houston, TX 77030 USA
[2] Univ Paris Sud, Breast Canc Unit, Dept Med Oncol, Inst Gustave Roussy, Villejuif, France
[3] Univ Paris Sud, Inst Gustave Roussy, Translat Res Unit, UPRES EA03535, Villejuif, France
[4] Inst Claudius Regault, Dept Med Oncol, Toulouse, France
[5] Ctr Claude Perrin, Dept Pathol, Clermont Ferrand, France
[6] Hosp Univ San Carlos, Dept Oncol, Madrid, Spain
[7] Univ Alberta, Dept Oncol, Edmonton, AB, Canada
关键词
D O I
10.1200/JCO.2007.14.9146
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose Several adjuvant chemotherapy trials suggested that cytotoxic treatment is less effective in patients with estrogen receptor ( ER) - positive breast cancers. The aim of the present study was to assess the efficacy of adjuvant docetaxel and anthracycline therapy according to ER expression in two randomized clinical trials. Patients and Methods Pooled data from two randomized trials, BCIRG001 and PACS01, were examined. Hazard ratios for recurrence and survival were estimated by Cox proportional hazards models and were adjusted for clinical variables. Interaction between docetaxel and ER expression was tested. Results ER status was available for 3,329 patients (95% of all randomly assigned patients), of whom 75% (n = 2,493) were ER positive. Docetaxel therapy was associated with a 30% reduction in the risk of death ( hazard ratio [HR] = 0.70; 95% CI, 0.54 to 0.91) in ER-positive patients and a 31% reduction ( HR = 0.69; 95% CI, 0.52 to 0.94) in ER-negative patients. Docetaxel therapy was associated with a 21% reduction in the risk of recurrence ( HR = 0.79; 95% CI, 0.66 to 0.93) in ER-positive patients and a 31% reduction ( HR = 0.69; 95% CI, 0.54 to 0.97) in ER-negative patients. The interaction between docetaxel therapy and ER status was not statistically significant for either overall survival ( P = .87) or disease-free survival ( P = .30). ER expression was also not predictive for docetaxel efficacy when it was analyzed as a semi-continuous variable based on percent of positive cells by immunohistochemistry ( test for heterogeneity, P =.56 and .86 for overall survival and disease-free survival, respectively). Conclusion In the pooled analysis of these two trials, docetaxel did not have a statistically significantly different effect on the risk of recurrence or death in ER-positive and ER-negative patients.
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页码:2636 / 2643
页数:8
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