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卡铂/培美曲塞联合或不联合贝伐珠单抗治疗晚期非鳞状非小细胞肺癌的疗效比较。

Comparative Effectiveness of Carboplatin/Pemetrexed With Versus Without Bevacizumab for Advanced Nonsquamous Non-Small Cell Lung Cancer.

机构信息

Division of Hematology/Oncology, Perelman School of Medicine at the University of Pennsylvania, and.

Abramson Cancer Center, Philadelphia, Pennsylvania.

出版信息

J Natl Compr Canc Netw. 2019 May 1;17(5):469-477. doi: 10.6004/jnccn.2018.7102.

Abstract

BACKGROUND

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).

MATERIALS AND METHODS

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.

RESULTS

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).

CONCLUSIONS

In this large, real-world dataset, the addition of bevacizumab to first-line carboplatin/pemetrexed for metastatic nonsquamous NSCLC was associated with improved OS.

摘要

背景

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)。

材料和方法

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。

结果

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)。

结论

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f5b/6661525/d154cbfc37b1/nihms-1038400-f0001.jpg

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