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表皮生长因子受体(EGFR)突变的早期非小细胞肺癌围手术期治疗:当前证据与未来展望

Perioperative Treatment in EGFR-Mutant Early-Stage Non-Small Cell Lung Cancer: Current Evidence and Future Perspectives.

作者信息

Guo Xiaobei, Liu Xiaoyan, Guo Chao, Miao Qian, Cheng Xinghua, Hong Xuan, Li Hongru, Qiu Xiaoming, Xiang Yi, Zheng Di, Zhou Jian, Jiang Liyan, Xu Yan, Wang Mengzhao

机构信息

Department of Respiratory and Critical Care Medicine, Peking Union Medical College Hospital, Chinese Academy of Medical Science and Peking Union Medical College, Beijing, China.

Department of Thoracic Surgery, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.

出版信息

Thorac Cancer. 2025 Feb;16(4):e70018. doi: 10.1111/1759-7714.70018.

Abstract

Adjuvant osimertinib administered over a 3-year period in patients diagnosed with stage IB-IIIA non-small cell lung cancer (NSCLC) and epidermal growth factor receptor (EGFR) mutations has not only shown improvement in event-free survival but also demonstrated a prolonged overall survival (OS), leading to its approval as a standard treatment in this context. Meanwhile, no targeted studies have been conducted on the efficacy of adjuvant immune checkpoint inhibitors in these patients. Although studies such as IMPOWER-010 and KEYNOTE-091 have included a small number of patients with positive driver genes, no definitive conclusions regarding the OS benefit have been established. Neoadjuvant targeted therapy is not currently recommended because of insufficient evidence, characterized by a low depth of pathological response and no reported improvement in survival outcomes. The same is true for neoadjuvant immunotherapy in patients with EGFR mutations. Although numerous issues such as refining patient population selection, determining appropriate combination therapy regimens, establishing primary endpoints, assessing the influence of perioperative complications, and accurately evaluating the clinical application of circulating tumor DNA in various scenarios exist, several promising ongoing trials, including ADAURA2 and NEOADURA, are expected to provide valuable insights that will help address these questions. Here, we summarize the available evidence and clinical issues that need to be considered to optimize clinical decision-making for patients with EGFR-mutant NSCLC.

摘要

对于诊断为IB-IIIA期非小细胞肺癌(NSCLC)且有表皮生长因子受体(EGFR)突变的患者,给予为期3年的辅助奥希替尼治疗,不仅显示无事件生存期有所改善,而且总生存期(OS)也延长,因此被批准作为这一情况下的标准治疗方法。与此同时,尚未针对这些患者开展辅助免疫检查点抑制剂疗效的针对性研究。尽管IMPOWER-010和KEYNOTE-091等研究纳入了少数驱动基因阳性的患者,但尚未得出关于OS获益的确切结论。由于证据不足,目前不推荐新辅助靶向治疗,其特点是病理反应深度低且未报告生存结局有改善。EGFR突变患者的新辅助免疫治疗情况也是如此。尽管存在诸多问题,如优化患者群体选择、确定合适的联合治疗方案、确立主要终点、评估围手术期并发症的影响以及准确评估循环肿瘤DNA在各种情况下的临床应用等,但包括ADAURA2和NEOADURA在内的一些正在进行的有前景的试验,有望提供有价值的见解,以帮助解决这些问题。在此,我们总结现有证据以及为EGFR突变的NSCLC患者优化临床决策时需要考虑的临床问题。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f27b/11842451/d9ef9bc85b85/TCA-16-e70018-g002.jpg

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