Dieras Veronique, Pop Simona, Berger Frederique, Dujaric Marie-Eglantine, Beuzeboc Philippe, Escalup Laurence, Bidard François Clement, Cottu Paul Henri, LE Tourneau Christophe, Piperno-Neumann Sophie, Laurence Valerie, Robain Mathieu, Asselain Bernard, Pierga Jean-Yves
Department of Medical Oncology, Curie Institute, PSL Research University, Paris, France
Department of Medical Oncology, Curie Institute, PSL Research University, Paris, France.
Anticancer Res. 2017 Mar;37(3):1403-1407. doi: 10.21873/anticanres.11462.
To assess outcomes in patients treated with first-line bevacizumab-containing therapy for human epidermal growth factor receptor (HER)2-negative metastatic breast cancer (mBC) at a single centre with a homogenous standard-of-care.
Information on patient and disease characteristics, efficacy, and safety was extracted from computer-based records of all patients receiving first-line bevacizumab-paclitaxel at the Curie Institute, Paris, France, between 2008 and 2011.
Median progression-free survival in the 116 treated patients was 13.2 months; median overall survival was 38.4 months. Corresponding values were 9.0 and 18.8 months, respectively, in patients with triple-negative mBC, and 19.4 and 58.8 months, respectively, in patients receiving maintenance endocrine therapy. No new safety signals were seen.
Outcomes in patients treated with bevacizumab-paclitaxel at our center were consistent with efficacy in prospective clinical trials, with notable activity in poor-prognosis disease. Maintenance endocrine or oral therapy with bevacizumab after paclitaxel discontinuation was associated with long-term disease control.
在单一中心采用统一标准治疗方案,评估一线含贝伐单抗治疗人表皮生长因子受体(HER)2阴性转移性乳腺癌(mBC)患者的疗效。
从2008年至2011年在法国巴黎居里研究所接受一线贝伐单抗联合紫杉醇治疗的所有患者的计算机记录中提取患者及疾病特征、疗效和安全性信息。
116例接受治疗的患者的中位无进展生存期为13.2个月;中位总生存期为38.4个月。三阴性mBC患者的相应数值分别为9.0个月和18.8个月,接受维持内分泌治疗的患者分别为19.4个月和58.8个月。未发现新的安全信号。
在我们中心接受贝伐单抗联合紫杉醇治疗的患者疗效与前瞻性临床试验一致,对预后不良疾病有显著活性。紫杉醇停药后采用维持内分泌治疗或口服贝伐单抗与长期疾病控制相关。