First-line treatment for driver gene–negative metastatic lung adenocarcinoma with malignant pleural effusion: Should chemotherapy be combined with an immune checkpoint inhibitor or bevacizumab?

Author:

Zhao Yuanyuan1,Mei Ting2,Na Feifei1,Tian Xiaoman3,Ao Rui4,Long Xiangyu5,Luo Qiang6,Duan Ping7,Zhu Jiang8,Wang Yongsheng1,Huang Meijuan1,Liu Yongmei1,Gong Youling1

Affiliation:

1. West China Hospital of Sichuan University

2. West China Tianfu Hospital, Sichuan University

3. Chengdu Jinniu District People's Hospital

4. Sichuan Academy of Medical Sciences & Sichuan Provincial People's Hospital

5. Sichuan Provincial Guang'An People's Hospital

6. Chengdu Xinjin District Hospital of Traditional Chinese Medicine

7. Chengdu First People's Hospital

8. West China Shangjin Hospital, Sichuan University

Abstract

Abstract Introduction: Patients with metastatic lung adenocarcinoma (MLA) and malignant pleural effusion (MPE) without driver gene mutations have a poor prognosis. None of the standard treatment strategies are recommended for such patients. We retrospectively analyzed the efficacy of the first-line treatment for this specific population: standard platinum-based doublet chemotherapy (CT), CT plus an immune checkpoint inhibitor (CT + ICI) and CT plus antiangiogenic agents (CT + Bev). Methods A total of 369 eligible patients were enrolled: CT alone (n = 201), CT + Bev (n = 83), and CT + ICI (n = 85). Treatment efficacy assessments were performed every two cycles according to the RECIST guidelines. The endpoints were overall survival (OS) and progression-free survival (PFS). Kaplan‒Meier curves and the log-rank test were used to compare OS and PFS. p < 0.05 was the threshold of significance (statistical software: SPSS). Results The median follow-up was 11.4 months (range of 2.1–49.6 months). PFS and OS in the CT + ICI/CT + Bev cohort were significantly longer than those in the CT group (PFS: 7.7/7.4/4.6 months, p = 0.001; OS: 18.5/17.8/10.9 months, p < 0.001, respectively). CT + Bev had better PFS and OS than CT + ICI/CT in PD-L1 < 1% patients (PFS: 8.4/4.8/4.8 months, p = 0.029; OS: 15.5/12.9/9.8 months, p = 0.002). Among patients with PD-L1 1–49%, CT + ICI led to a longer PFS and OS (PFS: 8.8/6.4/4.2 months, p = 0.002; OS: 34.1/21.0/11.5 months, p = 0.049). In the cohort with PD-L1 ≥ 50%, CT + ICI was still the best first-line treatment (PFS: 19.9/9.4/8.0 months, p = 0.029; OS: 30.2/15.5/13.0 months, p = 0.034). Conclusion In driver gene–negative MLA with MPE, CT + Bev or ICI better controlled MPE and significantly prolonged survival compared to chemotherapy alone. PD-L1 expression (negative/positive) might be a key factor influencing the choice of CT plus Bev or ICI.

Publisher

Research Square Platform LLC

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