{"title":"非小细胞肺癌术后免疫治疗:当前标准与前景","authors":"J. Slomka , G. Eberst , V. Westeel , M. Wislez","doi":"10.1016/S1877-1203(25)00066-7","DOIUrl":null,"url":null,"abstract":"<div><div>Surgical resection is the cornerstone of the management of resectable stage I to III nonsmall cell lung cancer (NSCLC). Platinum-based chemotherapy, whether neoadjuvant or adjuvant, has long been combined with surgery for patients with resectable stage II-III disease, although the benefits are modest, with an overall survival gain of approximately 5 %. Recently, immunotherapy has been incorporated into neoadjuvant, adjuvant, and perioperative treatment regimens based on data showing improvements in event-free survival (EFS), disease-free survival (DFS), and overall survival in patients with localized or locally advanced, resectable NSCLC without oncogenic driver mutations. Two phase 3 trials demonstrated a benefit of adjuvant immunotherapy, leading to European approval, although these are not currently reimbursed in France. Six phase 3 trials CheckMate-816, AEGEAN, CheckMate-77T, NeoTORCH, KEYNOTE-671, and RATIONALE-315 have shown a benefit from adding an immune checkpoint inhibitor to chemotherapy in the neoadjuvant or perioperative setting. Based on the results of CheckMate-816, neoadjuvant nivolumab has been approved in combination with platinum-based chemotherapy for adult patients with resectable NSCLC at high risk of recurrence, whose tumors express PD-L1 > 1 % and are negative for <em>EGFR</em> mutations and <em>ALK</em> rearrangements.</div></div>","PeriodicalId":53645,"journal":{"name":"Revue des Maladies Respiratoires Actualites","volume":"17 2","pages":"Pages 2S98-2S105"},"PeriodicalIF":0.0000,"publicationDate":"2025-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"L'immunothérapie péri-opératoire des cancers bronchiques non à petites cellules (CBNPC) : standards actuels et perspectives\",\"authors\":\"J. Slomka , G. Eberst , V. Westeel , M. Wislez\",\"doi\":\"10.1016/S1877-1203(25)00066-7\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Surgical resection is the cornerstone of the management of resectable stage I to III nonsmall cell lung cancer (NSCLC). Platinum-based chemotherapy, whether neoadjuvant or adjuvant, has long been combined with surgery for patients with resectable stage II-III disease, although the benefits are modest, with an overall survival gain of approximately 5 %. Recently, immunotherapy has been incorporated into neoadjuvant, adjuvant, and perioperative treatment regimens based on data showing improvements in event-free survival (EFS), disease-free survival (DFS), and overall survival in patients with localized or locally advanced, resectable NSCLC without oncogenic driver mutations. Two phase 3 trials demonstrated a benefit of adjuvant immunotherapy, leading to European approval, although these are not currently reimbursed in France. Six phase 3 trials CheckMate-816, AEGEAN, CheckMate-77T, NeoTORCH, KEYNOTE-671, and RATIONALE-315 have shown a benefit from adding an immune checkpoint inhibitor to chemotherapy in the neoadjuvant or perioperative setting. Based on the results of CheckMate-816, neoadjuvant nivolumab has been approved in combination with platinum-based chemotherapy for adult patients with resectable NSCLC at high risk of recurrence, whose tumors express PD-L1 > 1 % and are negative for <em>EGFR</em> mutations and <em>ALK</em> rearrangements.</div></div>\",\"PeriodicalId\":53645,\"journal\":{\"name\":\"Revue des Maladies Respiratoires Actualites\",\"volume\":\"17 2\",\"pages\":\"Pages 2S98-2S105\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2025-10-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Revue des Maladies Respiratoires Actualites\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1877120325000667\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"Medicine\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Revue des Maladies Respiratoires Actualites","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1877120325000667","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"Medicine","Score":null,"Total":0}
L'immunothérapie péri-opératoire des cancers bronchiques non à petites cellules (CBNPC) : standards actuels et perspectives
Surgical resection is the cornerstone of the management of resectable stage I to III nonsmall cell lung cancer (NSCLC). Platinum-based chemotherapy, whether neoadjuvant or adjuvant, has long been combined with surgery for patients with resectable stage II-III disease, although the benefits are modest, with an overall survival gain of approximately 5 %. Recently, immunotherapy has been incorporated into neoadjuvant, adjuvant, and perioperative treatment regimens based on data showing improvements in event-free survival (EFS), disease-free survival (DFS), and overall survival in patients with localized or locally advanced, resectable NSCLC without oncogenic driver mutations. Two phase 3 trials demonstrated a benefit of adjuvant immunotherapy, leading to European approval, although these are not currently reimbursed in France. Six phase 3 trials CheckMate-816, AEGEAN, CheckMate-77T, NeoTORCH, KEYNOTE-671, and RATIONALE-315 have shown a benefit from adding an immune checkpoint inhibitor to chemotherapy in the neoadjuvant or perioperative setting. Based on the results of CheckMate-816, neoadjuvant nivolumab has been approved in combination with platinum-based chemotherapy for adult patients with resectable NSCLC at high risk of recurrence, whose tumors express PD-L1 > 1 % and are negative for EGFR mutations and ALK rearrangements.