首页|期刊导航|中国肺癌杂志|免疫衰老背景下老年晚期NSCLC患者对PD-1/PD-L1抑制剂反应的异质性及干预策略

免疫衰老背景下老年晚期NSCLC患者对PD-1/PD-L1抑制剂反应的异质性及干预策略OA

Heterogeneity of Response to PD-1/PD-L1 Inhibitors in Elderly Patients with Advanced NSCLC under the Background of Immunosenescence and Intervention Strategies

中文摘要英文摘要

老年晚期非小细胞肺癌(non-small cell lung cancer,NSCLC)患者的比例逐年上升,尽管程序性死亡受体-1(programmed death protein 1,PD-1)/程序性死亡配体1(programmed death ligand 1,PD-L1)抑制剂彻底改变了晚期NSCLC的治疗格局,为患者带来生存获益,但老年人群因存在免疫衰老特征,衰老引发的胸腺退化、T细胞库多样性降低、慢性炎症削弱了免疫治疗的应答效率;加之临床试验中高龄患者入组不足、循证医学证据匮乏,导致其对PD-1/PD-L1抑制剂的治疗应答呈现显著异质性.临床研究发现,65-74岁患者从PD-1/PD-L1抑制剂单药或联合治疗中获益较明显,而≥75岁高龄人群疗效减弱,且免疫相关不良事件发生率升高.为优化老年患者治疗,基于综合老年评估结果制定个体化干预策略,主要包括低剂量免疫单药治疗、选择性联合治疗模式及靶向免疫衰老的新型疗法.未来研究应填补高龄患者临床证据空白,并推动基于免疫衰老程度和老年生理变化的精准治疗方案,以改善这一特殊人群的治疗结局.

The proportion of elderly patients with advanced non-small cell lung cancer(NSCLC)is on the rise.While programmed death protein 1(PD-1)/programmed death ligand 1(PD-L1)inhibitors have revolutionized the management of advanced NSCLC and improved patient survival,but the elderly display prominent immunosenescence features.Age-associated thymic involution,diminished T-cell repertoire diversity,and chronic inflammation directly compromise the efficacy of immu-notherapy.Furthermore,the underrepresentation of elderly patients in clinical trials and the paucity of high-quality evidence-based data jointly contribute to significant heterogeneity in their therapeutic responses to PD-1/PD-L1 inhibitors.While patients aged 65-74 years maintain significant survival benefits from immunotherapy-whether as monotherapy or combined regimens-those aged≥75 years exhibit attenuated efficacy and heightened susceptibility to immune-related adverse events.To address these challenges,Comprehensive Geriatric Assessment(CGA)enables risk-adapted therapeutic strategies,guiding interventions such as adjusted-dose immunotherapy,selective combination therapies,and emerging approaches targeting senescence-associated im-mune dysfunction.Closing current evidence gaps,particularly for underrepresented octogenarians,remains imperative,as does advancing precision immunotherapy models founded on biological aging metrics rather than chronological age alone.Bridging these knowledge gaps will permit tailored treatment algorithms to optimize outcomes in this clinically complex population.

黄玉蓉;王媛;魏澳娇;熊雨露;段明智;许彤瑶;何文杰

650500 昆明,昆明医科大学||650118 昆明,昆明医科大学第三附属医院,云南省肿瘤医院,北京大学肿瘤医院云南医院老年肿瘤科650118 昆明,昆明医科大学第三附属医院,云南省肿瘤医院,北京大学肿瘤医院云南医院生物治疗中心650500 昆明,昆明医科大学||650118 昆明,昆明医科大学第三附属医院,云南省肿瘤医院,北京大学肿瘤医院云南医院老年肿瘤科650500 昆明,昆明医科大学||650118 昆明,昆明医科大学第三附属医院,云南省肿瘤医院,北京大学肿瘤医院云南医院老年肿瘤科650500 昆明,昆明医科大学||650118 昆明,昆明医科大学第三附属医院,云南省肿瘤医院,北京大学肿瘤医院云南医院中西医结合科650500 昆明,昆明医科大学||650118 昆明,昆明医科大学第三附属医院,云南省肿瘤医院,北京大学肿瘤医院云南医院老年肿瘤科650118 昆明,昆明医科大学第三附属医院,云南省肿瘤医院,北京大学肿瘤医院云南医院老年肿瘤科

免疫衰老肺肿瘤PD-1/PD-L1抑制剂个体化治疗

ImmunosenescenceLung neoplasmsPD-1/PD-L1 inhibitorsIndividualized treatment

《中国肺癌杂志》 2026 (3)

190-199,10

This paper was supported by the grant from Hengru Rescarch Fund of Kunming Medical University(No.YQHR-2025-M20,to Wenjie HE). 本文受昆明医科大学恒瑞科研基金项目(No.YQHR-2025-M20)资助

10.3779/j.issn.1009-3419.2026.101.05

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