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118P Role of PD-L1 and pathological complete response (pCR) with neoadjuvant (NEO) or perioperative (PERIOP) immune-checkpoint inhibitors (ICI) and platinum-based chemotherapy (PCT) in resectable non-small cell lung cancer (NSCLC): A systematic review and metanalysis

医学 化疗 免疫检查点 PD-L1 围手术期 肿瘤科 肺癌 阿替唑单抗 病态的 新辅助治疗 顺铂 完全响应 癌症研究 内科学 彭布罗利珠单抗 癌症 免疫疗法 外科 乳腺癌
作者
Antonio Nuccio,Giuseppe Viscardi,Robert Bruce Cameron,Fabio Salomone,A. Servetto,Francesco Maria Venanzi,S.T. Riva,Sara Oresti,F.R. Ogliari,Alessandra Bulotta,Biagio Ricciuti,Daniele Marinelli,M. Ferrara,Fabiana Vitiello,Tina Cascone,Marina Chiara Garassino,Giulia Veronesi,Valter Torri,Michela Cinquini,Roberto Ferrara
出处
期刊:ESMO open [Elsevier BV]
卷期号:9: 102697-102697 被引量:1
标识
DOI:10.1016/j.esmoop.2024.102697
摘要

A previous metanalysis showed no significant subgroup interaction between PD-L1 and pCR, while both PD-L1 status and pCR significantly correlated with better event free survival (EFS). Overall, no difference in EFS between NEO and PERIOP strategies was reported by indirect comparison (Nuccio et al). Additional RCTs and updated results of previous studies could help to define the role of PD-L1 and pCR and the best treatment strategy according to these variables. PubMed, Embase and Cochrane were searched until 11/2023 for RCTs comparing NEO or PERIOP ICI + PCT with NEO PCT in patients (pts) with resectable NSCLC. Association between PD-L1 tumor proportional score (TPS) and pCR and correlation between PD-L1, pCR and EFS was assessed. Indirect comparison between PERIOP and NEO strategies was performed in PD-L1 and pCR subgroups. 8 RCTs (n=3407) were included. PERIOP/NEO significantly improved both pCR (χ2 = 10.45, p < 0.00001, I2= 33%) and EFS (χ2 = 6.33, p < 0.00001, I2= 5%).There was a significant subgroup interaction for pCR by PD-L1 TPS (<1%, 1-49% and ≥50%: χ2 = 6.44, p = 0.04, I2=68.9%). EFS significantly correlated with PD-L1 status (TPS <1% vs 1-49% vs ≥50%: χ2 = 13.28, p = 0.001, I2=84.9%) and pCR (χ2 =18.96, p < 0.0001, I2=94.7%). No difference in EFS between PERIOP and NEO strategies was observed either according to PDL1 status [TPS <1%: HR 1.03 (95% CI 0.68-1.56); 1-49%: HR 1.85 (95% CI 0.96-3.58); ≥50%: HR 1.54 (95% CI 0.77-3.05)] or according to pCR [pCR: HR 2.36 (95% CI 0.72-7.68); no-pCR: HR 0.86; (95% CI 0.60-1.23)]. Table: 118PpCR (RR)χ2p valueEFS (HR)χ2p valueOverall5.65 [4.09, 7.82]10.45< 0.000010.59[0.52, 0.67]6.33< 0.00001Pathological responseno-pCRNot applicable0.75 [0.64, 0.87]18.96< 0.0001pCR0.19 [0.11, 0.35]PD-L1<1%3.70 [2.41, 5.71]6.440.040.75 [0.62, 0.914.20.041-49%5.42 [2.66, 11.04]0.56 [0.42, 0.75]≥50%8.25 [5.30, 12.83]0.38 [0.28, 0.56] Open table in a new tab Updated results of previous studies and additional RCTs showed that PD-L1 status significantly correlates both with pCR and EFS and confirmed the achievement of pCR as a predictor of EFS benefit. NEO and PERIOP are equivalent strategies in all different PD-L1 and pCR categories.

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