首页> 外文期刊>Journal of Clinical Oncology >Phase III trial of observation versus six courses of paclitaxel in patients with advanced epithelial ovarian cancer in complete response after six courses of paclitaxel/platinum-based chemotherapy: final results of the After-6 protocol 1.
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Phase III trial of observation versus six courses of paclitaxel in patients with advanced epithelial ovarian cancer in complete response after six courses of paclitaxel/platinum-based chemotherapy: final results of the After-6 protocol 1.

机译:对晚期上皮性卵巢癌患者进行6疗程紫杉醇/铂基化疗后完全反应的观察与6疗程紫杉醇的III期观察试验:After-6方案的最终结果1。

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PURPOSE: To assess whether six courses of paclitaxel are effective as consolidation treatment in patients with advanced epithelial ovarian cancer who are in complete response after first-line paclitaxel/platinum-based chemotherapy. PATIENTS AND METHODS: Patients with stages IIb to IV disease in clinical or pathologic complete response after six courses of paclitaxel/platinum-based chemotherapy were randomly allocated to either observation (ie, control) or six courses of paclitaxel 175 mg/m(2) every 3 weeks (ie, maintenance). RESULTS: Two hundred patients were randomly assigned from March 1999 to July 2006. Because of the low accrual rate, an unplanned interim analysis of futility according to the Bayesian approach was performed. Grade 2 or greater motor neurotoxicity and sensory neurotoxicity were reported in 11.3% and 28.0% of the paclitaxel-arm patients, respectively. After a median follow-up of 43.5 months, 107 patients (53%) had experienced relapse, and 48 patients (24%) had died. Two-year progression-free survival rates were 54% (95% CI, 43% to 64%) and 59% (95% CI, 49% to 69%; P = not significant) in the control and maintenance arms, respectively. Corresponding 2-year overall survival rates were 90% (95% CI, 84% to 97%) and 87% (95% CI, 80% to 94%; P = not significant), respectively. The Cox model showed that residual disease after initial surgery (macroscopic v no macroscopic residuum; hazard ratio [HR], 1.91; 95%CI, 1.21 to 3.03) and stage (IIIc to IV v others; HR, 3.10; 95% CI, 1.13 to 8.48) were independent prognostic factors for progression-free survival, whereas the treatment arm (maintenance v control) had no prognostic relevance. CONCLUSION: A consolidation treatment with six cycles of paclitaxel does not prolong progression-free survival or overall survival in patients in complete response after first-line paclitaxel/platinum-based regimens.
机译:目的:评估一线紫杉醇/铂类一线化疗后完全缓解的晚期上皮性卵巢癌患者是否有六个疗程的紫杉醇作为巩固治疗有效。患者与方法:将六疗程紫杉醇/铂类化疗后临床或病理完全缓解的IIb至IV期疾病患者随机分配至观察(即对照)或六疗程紫杉醇175 mg / m(2)每3周一次(即维护)。结果:从1999年3月至2006年7月,随机分配了200名患者。由于应计率低,根据贝叶斯方法进行了无计划的无用期中期分析。紫杉醇组患者分别报告有2级或以上的运动神经毒性和感觉神经毒性,分别为11.3%和28.0%。中位随访43.5个月后,有107例患者(53%)经历了复发,48例患者(24%)死亡。对照组和维持组的两年无进展生存率分别为54%(95%CI,43%至64%)和59%(95%CI,49%至69%; P =不显着)。相应的2年总生存率分别为90%(95%CI,84%至97%)和87%(95%CI,80%至94%; P =不显着)。 Cox模型显示,初次手术后残余疾病(宏观观察无宏观残留;危险比[HR]为1.91; 95%CI为1.21至3.03)和分期(IIIc至IV为其他; HR为3.10; 95%CI为1.13至8.48)是无进展生存的独立预后因素,而治疗组(维持与对照)无预后相关性。结论:以紫杉醇/铂为一线一线治疗方案的患者,在六个疗程的紫杉醇巩固治疗不能延长无进展生存期或总生存期。

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