Division of Integrated Oncology, Institute of Biomedical Research and Innovation, 2-2, Minatojima-minamimachi, Chuo-ku, Kobe, Japan.
Anticancer Res. 2014 Jan;34(1):275-81.
The aim of this retrospective study was to evaluate bevacizumab combined with weekly paclitaxel with and without carboplatin in pre-treated patients with non-squamous non-small cell lung cancer (NSCLC).
Between November 2009 and October 2011, 43 pre-treated patients with non-squamous NSCLC received bevacizumab (15 mg/kg, day 1) plus weekly paclitaxel (60-80 mg/m(2), days 1, 8, 15) with carboplatin (area under the curve=4-5, day 1) (n=36), or bevacizumab plus weekly paclitaxel (n=7) alone every four weeks.
The response rate and disease control rates were 48.8% (21/43) and 86.0% (37/43), respectively. Median progression-free survival was 5.7 months, and overall survival was 14.5 months. Grade 3/4 neutropenia was observed in 37.2% of patients and peripheral neurotoxicity in 0%. No bevacizumab-related death was observed.
Even for heavily pre-treated patients, bevacizumab plus weekly paclitaxel with or without carboplatin was effective and tolerable in non-squamous NSCLC.
本回顾性研究旨在评估贝伐珠单抗联合每周紫杉醇联合或不联合卡铂治疗经治的非鳞状非小细胞肺癌(NSCLC)患者的疗效。
2009 年 11 月至 2011 年 10 月,43 例经治的非鳞状 NSCLC 患者接受贝伐珠单抗(15mg/kg,第 1 天)联合每周紫杉醇(60-80mg/m²,第 1、8、15 天)联合卡铂(曲线下面积=4-5,第 1 天)(n=36)或贝伐珠单抗联合每周紫杉醇(n=7)单独治疗,每 4 周一次。
客观缓解率和疾病控制率分别为 48.8%(21/43)和 86.0%(37/43)。中位无进展生存期为 5.7 个月,总生存期为 14.5 个月。37.2%的患者发生 3/4 级中性粒细胞减少症,0%的患者发生周围神经毒性。无贝伐珠单抗相关死亡。
即使是经过大量治疗的患者,贝伐珠单抗联合每周紫杉醇联合或不联合卡铂治疗非鳞状 NSCLC 仍然有效且耐受良好。