基于分子分型的广泛期小细胞肺癌免疫治疗专家共识OA
Expert Consensus on Immunotherapy for Extensive-stage Small Cell Lung Cancer Based on Molecular Subtyping
免疫检查点抑制剂联合铂类-依托泊苷化疗已成为广泛期小细胞肺癌(extensive-stage small cell lung cancer,ES-SCLC)的一线标准治疗方案.然而患者的治疗获益差异显著,长期生存率仍然有限.近年来,基于ASCL1、NEUROD1和POU2F3转录因子的表达特征以及免疫炎症状态建立的SCLC-A、SCLC-N、SCLC-P和SCLC-I分型体系,为解释ES-SCLC免疫治疗异质性和开展精准分层治疗提供新的依据.为规范分子分型在ES-SCLC免疫治疗中的临床转化,本共识组织呼吸内科、肿瘤内科、病理科、放疗科及基础医学等多学科专家,基于国内外循证医学证据和临床经验,围绕ES-SCLC一线免疫治疗现状、分子分型体系及免疫微环境特征、检测实施路径、免疫治疗相关生物标志物、分型治疗策略关键问题形成推荐意见.本共识强调,分子分型现阶段应定位为标准治疗基础上的生物学和临床研究分层工具,不宜作为独立治疗决策依据;免疫组化可作为具备条件中心开展分型探索和转化研究的重要方法之一;SCLC-I亚型可作为免疫治疗潜在获益人群的重要生物标志物之一;针对不同分型,delta样配体3(delta-like ligand 3,DLL3)靶向治疗、表观遗传调控、MYC/AURKA轴以及聚腺苷二磷酸核糖聚合酶(poly(ADP-ribose)polymerase,PARP)抑制剂可作为后续治疗优化的重要探索方向.本共识旨在推动ES-SCLC分子分型病理检测与临床应用的规范化,促进基于分子分型的免疫治疗分层管理和个体化治疗策略优化,为构建ES-SCLC精准免疫治疗体系提供依据.
Immune checkpoint inhibitors combined with Platinum-based Etopositde chemotherapy have become the first-line standard treatment for extensive-stage small cell lung cancer(ES-SCLC).However,treatment benefit varies sub-stantially among patients,and the proportion of long-term survivors remains limited.In recent years,the molecular classifica-tion framework comprising SCLC-A,SCLC-N,SCLC-P and SCLC-I,based on the expression patterns of ASCL1,NEUROD1 and POU2F3 as well as immune-inflammatory status,has provided a new basis for understanding the heterogeneity of im-munotherapy response and for developing precision stratified treatment in ES-SCLC.To standardize the clinical translation of molecular subtyping in ES-SCLC immunotherapy,this consensus was developed by multidisciplinary experts from respiratory medicine,oncology,pathology,radiation oncology,and basic medical sciences.Based on domestic and international evidence and clinical experience,the consensus provides recommendations on key issues,including first-line immunotherapy for ES-SCLC,molecular subtyping systems and immune microenvironment characteristics,testing and implementation pathways,immunotherapy-related biomarkers,subtype-informed treatment strategies,and dynamic monitoring.This consensus empha-sizes that molecular subtyping should currently be positioned as a tool for biological and clinical research stratification based on standard treatment,and should not be used as an independent basis for treatment decisions.Immunohistochemistry can serve as an important method for qualified centers to conduct subtyping exploration and translational research.The SCLC-I subtype may provide a useful reference for biomarker-based stratification and immunotherapy benefit prediction.For different subtypes,delta-like ligand 3(DLL3)-targeted therapy,epigenetic regulation,the MYC/AURKAaxis,and poly(ADP-ribose)polymerase(PARP)inhibitors can be important choices for subsequent treatment optimization.This consensus aims to stan-dardize pathological testing and clinical application of molecular subtyping in ES-SCLC,facilitate stratified management and individualized treatment optimization based on molecular subtypes,and provide a foundation for building a precision immu-notherapy system.
中国临床肿瘤学会肿瘤生物标志物专家委员会;浙江省抗癌协会肿瘤呼吸病学专业委员会;周建娅
肺肿瘤分子分型免疫治疗病理检测专家共识
Lung neoplasmsMolecular subtypingImmunotherapyPathological testingExpert consensus
《中国肺癌杂志》 2026 (7)
475-490,16
本文受浙江省科学技术厅"尖兵领雁+X"科技计划项目(No.2025C02094、No.2023C03069)、国家自然科学基金项目(No.82573076)及非传染性慢性疾病-国家科技重大专项(No.2026ZD0555906)资助 This paper was supported by the grants from the Key Research and Development Program of Zhejiang Province(No.2025C02094,to Jingjing QUNo.2023C03069,to Jianya ZHOU),National Natural Science Foundation of China(No.82573076,to Jingjing QU)and Noncommunicable Chronic Diseases-National Science and Technology Major Project(No.2026ZD0555906,to Jianya ZHOU).
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