医学
肺癌
腺癌
相关性
免疫组织化学
活检
内科学
克隆(Java方法)
癌
肿瘤科
肺
癌症
病理
胃肠病学
基因
生物
几何学
生物化学
数学
作者
Marius Ilié,Véronique Hofman,Christophe Bontoux,Samantha Goffinet,Jonathan Benzaquen,Simon Heeke,Jacques Boutros,Sandra Lassalle,Élodie Long-Mira,Katia Zahaf,Salomé Lalvée,Virginie Lespinet-Fabre,Olivier Bordone,Virginie Tanga,Abel Gómez-Caro,Charlotte Cohen,Jean‐Philippe Berthet,Charles‐Hugo Marquette,Paul Hofman
出处
期刊:Lung Cancer
[Elsevier]
日期:2023-07-01
卷期号:181: 107230-107230
被引量:3
标识
DOI:10.1016/j.lungcan.2023.107230
摘要
Both MET expression and the PD-L1 tumor proportion score (TPS) are companion diagnostics for treatment of advanced non-small cell lung carcinoma (aNSCLC) patients. We evaluated the rate of correlation between MET expression and the PD-L1 TPS in matched biopsies and surgically resected specimens from NSCLC patients.This retrospective analysis assessed the prevalence and correlation between MET expression (SP44 clone) and the PD-L1 TPS (22C3 clone) by immunohistochemistry together with molecular alterations determined by targeted next-generation sequencing in matched lung biopsy and surgically lung resected specimens from 70 patients with NSCLC.The study found a significant correlation between the MET H-score in surgical samples and matched biopsies (P-value < 0.0001), as well as between the PD-L1 TPS in paired biopsies and surgical samples (P-value < 0.0001). However, there was no significant correlation between the MET H-score or expression subgroups and the PD-L1 TPS in both types of paired samples (P-value = 0.47, and P-value = 0.90). The MET H-score was significantly higher in adenocarcinoma compared to squamous cell carcinoma (P-value < 0.0001). A mutational analysis showed that the MET H-score was significantly higher in NSCLC cases with targetable molecular alterations (P-value = 0.0095), while no significant correlation was found for the PD-L1 TPS.Our study found no significant correlation between PD-L1 and MET expression in samples from NSCLC patients, highlighting the importance of personalized treatment strategies based on individual expression profiles. These findings provide valuable insight into the development of effective immunotherapy and targeted therapy for NSCLC patients.
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