贝伐单抗
阿替唑单抗
医学
卡铂
依托泊苷
肿瘤科
内科学
化疗
单克隆抗体
血管内皮生长因子
肺癌
血管内皮生长因子受体
顺铂
抗体
癌症
免疫学
免疫疗法
无容量
作者
G. Lamberti,K. Rihawi,F. Riccardi,F. Mazzoni,A. Follador,A. Bonetti,D. Giardina,C. Genova,Federica Bertolini,A. Frassoldati,M. Brighenti,I. Colantonio,G. Pasello,C. Ficorella,S. Cinieri,M. Tiseo,S. Fancelli,E. Andrini,Giada Targato,M. Tognetto,Luca Boni,A. Ardizzoni
标识
DOI:10.1016/j.jtho.2023.09.250
摘要
The addition of programmed-death ligand 1 (PD-L1) inhibition to platinum-etoposide improved survival in extensive stage small-cell lung cancer (ES-SCLC). Vascular endothelial growth factor (VEGF) has immunosuppressive effects in SCLC tumor micro-environment. We have previously demonstrated safety and signals of activity of adding bevacizumab, an anti-VEGF monoclonal antibody, to platinum-etoposide chemotherapy in the phase III FARM6PMFJM trial. Because combining PD-L1 and VEGF inhibition has synergistic antitumor effect in SCLC models, we hypothesized that adding bevacizumab to atezolizumab, carboplatin and etoposide would improve survival in patients with ES-SCLC.
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