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可切除及IIIA-N2期非小细胞肺癌围手术期免疫治疗与酪氨酸激酶抑制剂治疗策略综述

A review of perioperative treatment strategies with immunotherapy and tyrosine kinase inhibitors in resectable and stage IIIA-N2 non-small cell lung cancer.

作者信息

Hopson Madeleine B, Rashdan Sawsan

机构信息

Division of Hematology and Oncology, Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, TX, United States.

Harold C. Simmons Comprehensive Cancer Center, University of Texas Southwestern Medical Center, Dallas, TX, United States.

出版信息

Front Oncol. 2024 Mar 27;14:1373388. doi: 10.3389/fonc.2024.1373388. eCollection 2024.

Abstract

Stage IIIA-N2 non-small cell lung cancer (NSCLC) is a heterogeneous group with different potential therapeutic approaches. Treatment is typically multimodal with either surgical resection after neoadjuvant chemotherapy and/or radiation or concurrent chemotherapy and radiation if unresectable. Despite the multimodal treatment and early stage, cure rates have traditionally been low. The introduction of immunotherapy changed the treatment landscape for NSCLC in all stages, and the introduction of immunotherapy in early-stage lung cancer has improved event free survival and overall survival. Tyrosine Kinase inhibitors (TKIs) have also improved outcomes in early-stage mutation-driven NSCLC. Optimal treatment choice and sequence is increasingly becoming based upon personalized factors including clinical characteristics, comorbidities, programmed death-ligand 1 (PD-L1) score, and the presence of targetable mutations. Despite encouraging data from multiple trials, the optimal multimodal sequence of stage IIIA-N2 NSCLC treatment remains unresolved and warrants further investigation. This review article summarizes recent major clinical trials of neoadjuvant and adjuvant treatment including stage IIIA-N2 NSCLC with a focus on immunotherapy and TKIs.

摘要

IIIA-N2期非小细胞肺癌(NSCLC)是一组具有不同潜在治疗方法的异质性疾病。治疗通常采用多模式,对于可切除的患者,在新辅助化疗和/或放疗后进行手术切除;对于不可切除的患者,则采用同步放化疗。尽管采用了多模式治疗且处于早期阶段,但传统上治愈率一直较低。免疫疗法的引入改变了NSCLC各阶段的治疗格局,早期肺癌中免疫疗法的引入提高了无事件生存期和总生存期。酪氨酸激酶抑制剂(TKIs)也改善了早期突变驱动的NSCLC的治疗效果。最佳治疗选择和顺序越来越基于个性化因素,包括临床特征、合并症、程序性死亡配体1(PD-L1)评分以及可靶向突变的存在。尽管多项试验取得了令人鼓舞的数据,但IIIA-N2期NSCLC治疗的最佳多模式顺序仍未解决,值得进一步研究。这篇综述文章总结了近期新辅助和辅助治疗的主要临床试验,包括IIIA-N2期NSCLC,重点关注免疫疗法和TKIs。

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