首页> 外文期刊>Cancer chemotherapy and pharmacology. >The Breast Avastin Trial: phase II study of bevacizumab maintenance therapy after induction chemotherapy with docetaxel and capecitabine for the first-line treatment of patients with locally recurrent or metastatic breast cancer.
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The Breast Avastin Trial: phase II study of bevacizumab maintenance therapy after induction chemotherapy with docetaxel and capecitabine for the first-line treatment of patients with locally recurrent or metastatic breast cancer.

机译:乳腺Avastin试验:II期贝伐单抗维持治疗诱导化疗后的多西紫杉醇和Capecitabine进行局部复发性或转移性乳腺癌患者的一线治疗。

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Therapeutic approach for patients with metastatic breast cancer (MBC) is still controversial. This study was conducted to assess the efficacy and safety of bevacizumab in combination with docetaxel plus capecitabine as first-line treatment for MBC. The feasibility of bevacizumab maintenance therapy in this setting was also evaluated.In this single-arm, multicenter phase II study, patients received bevacizumab 15 mg/kg and docetaxel 60 mg/m(2) on day 1, plus capecitabine 900 mg/m(2) twice daily on days 1-14 every 21 days. Treatment was administered for up to 6 cycles, then bevacizumab continued until progressive disease. The primary end point was progression-free survival (PFS); secondary end points were tumor response rate, overall survival, and toxicity.Seventy-nine eligible patients were treated with bevacizumab in combination with docetaxel plus capecitabine. The overall response rate was 61 %, with a complete response rate of 8 % and a median duration of response of 10 months. At a median follow-up of 28 months, the median PFS was 11 months. Fifty-two (65 %) patients received bevacizumab maintenance therapy for a median duration of 7 months (range 1 to 33+). Neutropenia was the most common grade 3-4 toxicity (28.1 % of patients), and two fatal adverse events occurred (septic shock and gastrointestinal perforation).Bevacizumab in combination with docetaxel and capecitabine demonstrates significant activity and quite acceptable toxicity profile as first-line treatment of MBC. Subsequent maintenance therapy with bevacizumab is feasible for a long period of stable disease. Results deserve confirmation.
机译:转移乳腺癌患者的治疗方法(MBC)仍然存在争议。进行了本研究以评估Bevacizumab与多西紫杉醇加己二津的疗效和安全性作为MBC的一线治疗。还评估了Bevacizumab维护治疗的可行性。在第1天,患者在第1天,患者接受了贝伐单抗15mg / kg和多西紫杉醇60mg / m(2)的单臂,患者60 mg / m(2)。 (2)每天每天每天两次每21天。施用治疗最多6个循环,然后贝伐单抗持续直至进行渐进疾病。主要终点是无进展的存活率(PFS);次要终点是肿瘤反应率,总体存活和毒性。将九岁符合条件的患者与Docetaxel Plus Capecitabine组合使用Bevacizumab治疗。整体反应率为61%,响应率较为8%,中位数持续时间为10个月。在28个月的中位随访,中位数PFS为11个月。五十二(65%)患者接受贝伐单抗维持治疗,中位持续时间为7个月(范围1至33 +)。中性粒细胞蛋白是最常见的3-4级毒性(28.1%的患者),并且发生了两个致命的不良事件(脓肌休克和胃肠穿孔).Bevacizumab与Docetaxel和Capecitabine相结合,证明了重要的活动和相当可接受的毒性概况作为一线治疗MBC。随后的维持治疗贝伐单抗是可行的长期稳定的疾病。结果值得确认。

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