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贝伐单抗联合节拍化疗用于蒽环类和紫杉类难治性乳腺癌患者的治疗

Bevacizumab in combination with metronomic chemotherapy in patients with anthracycline- and taxane-refractory breast cancer.

作者信息

García-Sáenz J A, Martín M, Calles A, Bueno C, Rodríguez L, Bobokova J, Custodio A, Casado A, Díaz-Rubio E

机构信息

Service de Oncología Médica, Hospital Clínico San Carlos, Madrid, Spain.

出版信息

J Chemother. 2008 Oct;20(5):632-9. doi: 10.1179/joc.2008.20.5.632.

Abstract

A vascular endothelial growth factor (VEGF) inhibitor might enhance metronomic chemotherapy in previously treated metastatic breast cancer (MBC) patients. Anthracycline and taxane refractory MBC patients were given cyclophosphamide 50 mg p.o. daily, methotrexate 1 mg/kg i.v. every 14 days, and bevacizumab 10 mg/kg i.v. every 14 days. Trastuzumab was added in HER2-overexpressing tumors. 24 patients were enrolled and 22 were evaluable. All tumors had histologic grade II-III and most patients had > or =2 metastatic sites. After a median follow-up of 7.7 months the response rates were: complete response (CR) 0%, partial response (PR) 31.8% (95% CI 13.9- 54.9%), stable disease for >or =24 weeks (SD) 31.8% (95% CI 13.9-54.9%). Clinical benefit (CB= CR + PR + SD>24w) 63.6% (95% CI 40.7-82.8%). Median progression-free survival (PFS) was 7.5 months; overall survival (OS) was 13.6 months. HER2-overexpressing or high proliferative-index tumors had better 6-month PFS (75% vs. 34% in HER-negative tumors, P = 0.043; 67% vs. 0% in Ki-67 > or =20% tumors, P = 0.015). Adverse effects were mild. The combination of bevacizumab and a metronomic-based chemotherapy was effective, well tolerated and provided clinical benefit in heavilytreated MBC patients.

摘要

血管内皮生长因子(VEGF)抑制剂可能会增强节拍化疗对既往接受过治疗的转移性乳腺癌(MBC)患者的疗效。对蒽环类和紫杉类难治性MBC患者,给予口服环磷酰胺50mg/日,静脉注射甲氨蝶呤1mg/kg,每14天一次,以及静脉注射贝伐单抗10mg/kg,每14天一次。HER2过表达的肿瘤患者加用曲妥珠单抗。共纳入24例患者,22例可评估。所有肿瘤组织学分级为II - III级,大多数患者有≥2个转移部位。中位随访7.7个月后,缓解率为:完全缓解(CR)0%,部分缓解(PR)31.8%(95%CI 13.9 - 54.9%),疾病稳定≥24周(SD)31.8%(95%CI 13.9 - 54.9%)。临床获益(CB = CR + PR + SD>24周)63.6%(95%CI 40.7 - 82.8%)。中位无进展生存期(PFS)为7.5个月;总生存期(OS)为13.6个月。HER2过表达或高增殖指数的肿瘤患者6个月PFS较好(HER阴性肿瘤中为75% vs. 34%,P = 0.043;Ki-67≥20%的肿瘤中为67% vs. 0%,P = 0.015)。不良反应轻微。贝伐单抗与基于节拍化疗的联合方案有效,耐受性良好,为重度治疗的MBC患者提供了临床获益。

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