Difficult Decisions in the Multidisciplinary Treatment of Resectable Non-small Cell Lung Cancer.

IF 3.4 2区 医学 Q2 ONCOLOGY
Annals of Surgical Oncology Pub Date : 2025-07-01 Epub Date: 2025-04-28 DOI:10.1245/s10434-025-17345-2
Wara Naeem, Arsalan A Khan, Oluwamuyiwa W Adebayo, Minha Ansari, Nicole Geissen, Gillian Alex, Michael J Liptay, Mary Jo Fidler, Gaurav Marwaha, Christopher W Seder
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引用次数: 0

Abstract

The management of resectable non-small cell lung cancer (NSCLC) has evolved dramatically over the past three decades. Once limited to surgery, treatment strategies now include chemotherapy, immunotherapy, radiation, and targeted therapies. Despite advances in clinical trials and updated guidelines, several gray areas persist in practice. This review highlights two commonly encountered dilemmas, framed by recent trial data. The first dilemma is centered on the question: for a patient with a 4.1 cm node-negative tumor, is the optimal approach neoadjuvant, adjuvant, or perioperative chemoimmunotherapy? CheckMate 816 demonstrated improved pathological complete response and event-free survival with neoadjuvant chemoimmunotherapy. Perioperative approaches, combining neoadjuvant and adjuvant immunotherapy, showed promising outcomes in KEYNOTE-671, AEGEAN, and CheckMate 77T, whereas IMpower010 and KEYNOTE-091 demonstrated benefit with adjuvant therapy. Moreover, for patients with EGFR or ALK mutations, targeted therapies have shifted the treatment paradigm, as shown in the ADAURA and ALINA trials. However, no head-to-head comparisons among these strategies exist, limiting decision-making. The second dilemma involves a hypothetical scenario of a patient a with biopsy-proven T1cN2 disease: should treatment involve neoadjuvant chemoimmunotherapy followed by surgery, or chemoradiation followed by consolidation immunotherapy (durvalumab) or targeted agents (such as osimertinib)? The PACIFIC and LAURA trials support the latter approach for unresectable disease, while CheckMate 816 supports surgery for resectable N2 cases. Yet defining resectability remains subjective, especially with multistation or bulky N2 disease. While the upcoming AJCC 9th edition proposes a subdivision of N2 into N2a (single-station) and N2b (multi-station), offering a potential step forward, this refinement has yet to translate into clear clinical guidance. These scenarios highlight the need for prospective, stage stratified trials, designed to address these pertinent questions so that improved guidelines may help clinical decision making in borderline cases.

可切除非小细胞肺癌多学科治疗中的困难抉择。
在过去的三十年中,可切除的非小细胞肺癌(NSCLC)的治疗发生了巨大的变化。曾经仅限于手术,现在的治疗策略包括化疗、免疫疗法、放疗和靶向治疗。尽管在临床试验和最新指南方面取得了进展,但实践中仍存在一些灰色地带。根据最近的试验数据,这篇综述强调了两个经常遇到的困境。第一个困境集中在这样一个问题上:对于一个4.1 cm淋巴结阴性肿瘤患者,新辅助、辅助还是围手术期化疗免疫治疗是最佳方法?CheckMate 816在新辅助化疗免疫治疗下表现出改善的病理完全缓解和无事件生存期。在KEYNOTE-671、AEGEAN和CheckMate 77T中,围手术期方法联合新辅助和辅助免疫治疗显示出良好的结果,而IMpower010和KEYNOTE-091显示出辅助治疗的益处。此外,如ADAURA和ALINA试验所示,对于EGFR或ALK突变患者,靶向治疗已经改变了治疗模式。然而,这些策略之间不存在正面比较,限制了决策。第二个困境涉及一个假设的情况,患者a活检证实T1cN2疾病:治疗是否包括新辅助化疗免疫治疗后手术,或化疗放疗后巩固免疫治疗(杜伐单抗)或靶向药物(如奥西替尼)?PACIFIC和LAURA试验支持后一种方法治疗不可切除的疾病,而CheckMate 816则支持手术治疗可切除的N2病例。然而,对于可切除性的定义仍然是主观的,特别是对于多站点或大体积N2疾病。虽然即将到来的AJCC第9版提出将N2细分为N2a(单站)和N2b(多站),提供了潜在的进步,但这种改进尚未转化为明确的临床指导。这些情况强调了前瞻性、分期分层试验的必要性,旨在解决这些相关问题,以便改进指南可以帮助边缘病例的临床决策。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
5.90
自引率
10.80%
发文量
1698
审稿时长
2.8 months
期刊介绍: The Annals of Surgical Oncology is the official journal of The Society of Surgical Oncology and is published for the Society by Springer. The Annals publishes original and educational manuscripts about oncology for surgeons from all specialities in academic and community settings.
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