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

IF 2.3 3区 医学 Q3 ONCOLOGY Thoracic Cancer Pub Date : 2025-02-01 DOI:10.1111/1759-7714.70018
Xiaobei Guo, Xiaoyan Liu, Chao Guo, Qian Miao, Xinghua Cheng, Xuan Hong, Hongru Li, Xiaoming Qiu, Yi Xiang, Di Zheng, Jian Zhou, Liyan Jiang, Yan Xu, Mengzhao Wang
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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.

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egfr突变的早期非小细胞肺癌围手术期治疗:目前的证据和未来的展望。
对诊断为IB-IIIA期非小细胞肺癌(NSCLC)和表皮生长因子受体(EGFR)突变的患者进行为期3年的辅助奥希替尼治疗,不仅显示出无事件生存期的改善,而且显示出延长的总生存期(OS),导致其被批准为这种情况下的标准治疗。同时,还没有针对佐剂免疫检查点抑制剂在这些患者中的疗效进行针对性的研究。尽管像IMPOWER-010和KEYNOTE-091这样的研究包括了少数阳性驱动基因的患者,但关于OS的益处还没有明确的结论。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,没有报道改善生存结果。对于EGFR突变患者的新辅助免疫治疗也是如此。尽管存在许多问题,如优化患者群体选择,确定适当的联合治疗方案,建立主要终点,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,但一些有希望的正在进行的试验,包括ADAURA2和NEOADURA,有望提供有价值的见解,有助于解决这些问题。在这里,我们总结了现有的证据和需要考虑的临床问题,以优化egfr突变的非小细胞肺癌患者的临床决策。
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来源期刊
Thoracic Cancer
Thoracic Cancer ONCOLOGY-RESPIRATORY SYSTEM
CiteScore
5.20
自引率
3.40%
发文量
439
审稿时长
2 months
期刊介绍: Thoracic Cancer aims to facilitate international collaboration and exchange of comprehensive and cutting-edge information on basic, translational, and applied clinical research in lung cancer, esophageal cancer, mediastinal cancer, breast cancer and other thoracic malignancies. Prevention, treatment and research relevant to Asia-Pacific is a focus area, but submissions from all regions are welcomed. The editors encourage contributions relevant to prevention, general thoracic surgery, medical oncology, radiology, radiation medicine, pathology, basic cancer research, as well as epidemiological and translational studies in thoracic cancer. Thoracic Cancer is the official publication of the Chinese Society of Lung Cancer, International Chinese Society of Thoracic Surgery and is endorsed by the Korean Association for the Study of Lung Cancer and the Hong Kong Cancer Therapy Society. The Journal publishes a range of article types including: Editorials, Invited Reviews, Mini Reviews, Original Articles, Clinical Guidelines, Technological Notes, Imaging in thoracic cancer, Meeting Reports, Case Reports, Letters to the Editor, Commentaries, and Brief Reports.
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