ASCO 2014:辅助化疗+贝伐珠单抗未使HER2阴性乳腺癌患者获益

2014-06-06 CMT肿瘤 中国医学论坛报

HER2阴性乳腺癌化疗基础上增加贝伐珠单抗辅助治疗无获益 题目:贝伐珠单抗在HER2阴性乳腺癌辅助治疗中的应用:ECOG一E5103研究的最终结果(Bevacizumab (Bv) in the adjuvant treatment of HER2-negative breast cancer: Final results from Eastern Cooperative Oncology Gr

HER2阴性乳腺癌化疗基础上增加贝伐珠单抗辅助治疗无获益

题目:贝伐珠单抗在HER2阴性乳腺癌辅助治疗中的应用:ECOG一E5103研究的最终结果(Bevacizumab (Bv) in the adjuvant treatment of HER2-negative breast cancer: Final results from Eastern Cooperative Oncology Group E5103.)

摘要号:# 500

报告时间2014年5月31日

报告者:美国印第安纳大学Melvin and Bren Simon癌症中心 Kathy Miller

Session Title:Breast Cancer -HER2/ER

Session Type:Oral Abstract Session

背景:贝伐珠单抗(Bv)可延长转移性乳腺癌的PFS,但对OS无益。E5103 研究将Bv应用于HER2阴性乳腺癌的辅助治疗中。

方法:患者按1:2:2随机分为三组:A组(AC→T)即多柔比星联合环磷酰胺继之紫杉醇周疗方案+安慰剂;B组(BvAC→BvT),上述化疗期间联合Bv;C组(BvAC→BvT→Bv),化疗期间联合贝伐单抗,继之10个周期的贝伐单抗单药治疗。根据随化疗方案而调整的Bv剂量进行随机分层。C组中放疗和激素治疗与贝伐单抗同步进行。主要研究终点为无浸润性疾病生存率(IDFS)。HR为0.75,效力80%,采用log rank检验,单侧P值0.025,双侧P值0.05要求下需达到426例IDFS事件。

结果:共入组4994例患者。中位年龄52岁,ER+者64%,淋巴结阴性者27%,80%的患者接受了ddAC。化疗相关的毒副反应:骨髓抑制(4度粒细胞减低分别为17%、20%、21%),神经毒性(>3级分别为8%、8%、9%),三组之间相似。贝伐单抗治疗的患者中观察到3度以上的高血压,血小板减少,蛋白尿和出血,发生率分别为8%,3%,<1%,<1%。15个月时临床累积心衰发生率分别为1.0%、1.9%、3.0%。紧急揭盲发生率低,三组之间相似(分别为3%、4%、4% )。贝伐单抗治疗的完成情况低于预期,B组有24%,C组有55%的患者在治疗计划完成前提前终止了贝伐单抗治疗。中位随访时间47.5个月。共有430例IDFS事件,5年的IDFS率分别为77%(70.9%-81.2%)、76%(71.5%-79.8%)、80%(77%-82.5%)。

结论:对于高危的HER2阴性乳腺癌患者,在蒽环和紫杉类辅助化疗的基础上增加Bv不能改善IDFS和OS。Bv增加了治疗的毒副反应,但均在可预期范围内。鉴于各种原因导致的早期治疗终止的发生率较高,长时间治疗治疗方案似乎并不可取。

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    2015-01-23 quxin068
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