Division of Hematology/Oncology, Perelman School of Medicine at the University of Pennsylvania, and.
Abramson Cancer Center, Philadelphia, Pennsylvania.
J Natl Compr Canc Netw. 2019 May 1;17(5):469-477. doi: 10.6004/jnccn.2018.7102.
Despite recent advances in targeted therapy and immunotherapy for advanced non-small cell lung cancer (NSCLC), carboplatin/pemetrexed/bevacizumab remains a commonly used first-line regimen. However, it is unknown whether the addition of bevacizumab to carboplatin/pemetrexed improves overall survival (OS).
Using nationally representative curated electronic health record data from Flatiron Health, we performed a retrospective cohort study of patients diagnosed with advanced nonsquamous NSCLC who received ≥1 cycle of carboplatin/pemetrexed ± bevacizumab as initial systemic therapy for stage IV or metastatic/recurrent disease. The OS impact of adding bevacizumab to carboplatin/pemetrexed was assessed using a Cox proportional hazards model to adjust for age, sex, race, original tumor stage, time between diagnosis of metastatic disease and start of chemotherapy, and performance status. In a secondary analysis of patients at a single academic institution, we also adjusted for the presence of brain metastases, hemoptysis, and anticoagulation.
A total of 4,724 patients were included, of which 2,759 patients (58%) received carboplatin/pemetrexed and 1,965 (42%) received carboplatin/pemetrexed/bevacizumab. Median OS was 12.1 months (95% CI, 11.2-12.9 months) in the carboplatin/pemetrexed/bevacizumab group compared with 8.6 months (95% CI, 8.1-9.1 months) in the carboplatin/pemetrexed group (P<.001). Bevacizumab use remained associated with improved OS in a multivariate model (hazard ratio, 0.80; 95% CI, 0.75-0.86; P<.001). In the secondary, institutional analysis (N=539), the effect of bevacizumab was unchanged (hazard ratio, 0.75; 95% CI, 0.59-0.96; P=.02).
In this large, real-world dataset, the addition of bevacizumab to first-line carboplatin/pemetrexed for metastatic nonsquamous NSCLC was associated with improved OS.
尽管针对晚期非小细胞肺癌(NSCLC)的靶向治疗和免疫治疗取得了最近的进展,但卡铂/培美曲塞/贝伐珠单抗仍然是常用的一线治疗方案。然而,尚不清楚贝伐珠单抗联合卡铂/培美曲塞是否能改善总生存期(OS)。
我们使用来自 Flatiron Health 的具有代表性的、经过整理的电子健康记录数据,对接受至少 1 个周期卡铂/培美曲塞联合±贝伐珠单抗作为 IV 期或转移性/复发性疾病初始全身治疗的晚期非鳞状 NSCLC 患者进行了回顾性队列研究。使用 Cox 比例风险模型评估添加贝伐珠单抗对卡铂/培美曲塞的 OS 影响,以调整年龄、性别、种族、原始肿瘤分期、转移性疾病诊断和化疗开始之间的时间以及表现状态。在单一学术机构的患者的二次分析中,我们还调整了脑转移、咯血和抗凝的存在。
共纳入 4724 例患者,其中 2759 例(58%)接受卡铂/培美曲塞治疗,1965 例(42%)接受卡铂/培美曲塞/贝伐珠单抗治疗。卡铂/培美曲塞/贝伐珠单抗组的中位 OS 为 12.1 个月(95%CI,11.2-12.9 个月),而卡铂/培美曲塞组为 8.6 个月(95%CI,8.1-9.1 个月)(P<.001)。在多变量模型中,贝伐珠单抗的使用仍与改善的 OS 相关(风险比,0.80;95%CI,0.75-0.86;P<.001)。在二次机构分析(N=539)中,贝伐珠单抗的作用保持不变(风险比,0.75;95%CI,0.59-0.96;P=.02)。
在这个大型真实世界数据集中,转移性非鳞状 NSCLC 一线治疗中添加贝伐珠单抗联合卡铂/培美曲塞可改善 OS。