多西紫杉醇
医学
紫杉醇
转移性乳腺癌
内科学
养生
化疗
肿瘤科
紫杉烷
危险系数
乳腺癌
人口
癌症
置信区间
环境卫生
作者
Stephen E. Jones,John K. Erban,Beth Overmoyer,G. T. Budd,Laura F. Hutchins,EE Lower,Leslie Rodgers Laufman,S. Sundaram,W J Urba,Kathleen I. Pritchard,Robert Mennel,Donald Richards,Steven R. Olsen,Marlene Meyers,Peter M. Ravdin
标识
DOI:10.1200/jco.2005.02.027
摘要
PURPOSE: This randomized, controlled, multicenter, open-label, phase III study compared docetaxel versus paclitaxel in patients with advanced breast cancer that had progressed after an anthracycline-containing chemotherapy regimen. PATIENTS AND METHODS: Patients (n = 449) were randomly assigned to receive either docetaxel 100 mg/m2 (n = 225) or paclitaxel 175 mg/m2 (n = 224) on day 1, every 21 days until tumor progression, unacceptable toxicity, or withdrawal of consent. RESULTS: In the intent-to-treat population, both the median overall survival (OS, 15.4 v 12.7 months; hazard ratio [HR], 1.41; 95% CI, 1.15 to 1.73; P = .03) and the median time to progression (TTP, 5.7 months v 3.6 months; HR, 1.64; 95% CI, 1.33 to 2.02; P < .0001) for docetaxel were significantly longer than for paclitaxel, and the overall response rate (ORR, 32% v 25%; P = .10) was higher for docetaxel. These results were confirmed by multivariate analyses. The incidence of treatment-related hematologic and nonhematologic toxicities was greater for docetaxel than for paclitaxel; however, quality-of-life scores were not statistically different between treatment groups over time. CONCLUSION: Docetaxel was superior to paclitaxel in terms of OS and TTP. ORR was higher for docetaxel. Hematologic and nonhematologic toxicities occurred more frequently in the docetaxel group. The global quality-of-life scores were similar for both agents over time.
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