西妥昔单抗
伊立替康
结直肠癌
阿维鲁单抗
微卫星不稳定性
医学
免疫系统
癌症研究
肿瘤科
内科学
癌症
免疫学
免疫疗法
生物
无容量
微卫星
等位基因
基因
生物化学
作者
Nicolas D. Huyghe,Elena Benidovskaya,Tariq Masoodi,Isabelle Sinapi,Astrid De Cuyper,Fazulur Rehaman Vempalli,Simon P. Beyaert,Caroline Bouzin,Finoula Maestre Osorio,Luigi Ferraro,Nicolas van Baren,Raphaël Helaers,Pierre Goffette,Benoît Ghaye,Aline van Maanen,Marie-Laure Castella,Michele Ceccarelli,Davide Bedognetti,Jérôme Galon,Wouter Hendrickx
标识
DOI:10.1016/j.xcrm.2025.102201
摘要
The treatment of patients with microsatellite-stable (MSS) metastatic colorectal cancer (mCRC) remains a significant clinical challenge. Cetuximab, an anti-epidermal growth factor receptor (EGFR) monoclonal antibody (mAb), induces immunogenic cell death, potentially synergizing with immune checkpoint inhibitors. The phase 2, proof-of-concept, single-arm AVETUXIRI trial (ClinicalTrials.gov: NCT03608046) evaluates the safety and efficacy of cetuximab, irinotecan (a topoisomerase I inhibitor), and avelumab (an anti-programmed cell death ligand 1 [PD-L1]) in 57 patients with RAS wild-type or mutated MSS mCRC refractory to chemotherapy and anti-EGFR mAbs. Exploratory objectives include investigating the tumor immune microenvironment within mCRC biopsies performed during the trial and correlating it with treatment activity. A manageable safety profile is observed. Although the overall efficacy endpoints are not met, biomarkers associated with clinical efficacy are identified. Patients exhibiting a high Immunoscore, strong cytotoxic and T cell proximity to tumor cells, and a high genetic immunoediting score within mCRC biopsies before treatment demonstrate significant therapeutic survival benefit, independent of RAS tumor mutation status.
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