Barcellini Lucrezia, Nardin Simone, Sacco Gianluca, Ferrante Michele, Rossi Giovanni, Barletta Giulia, Bennicelli Elisa, Dellepiane Chiara, Tagliamento Marco, Ramella Pollone Beatrice, Lucente Luca, Coco Simona, Marconi Silvia, Santamaria Sara, Pariscenti Gian Luca, Genova Carlo
Department of Internal Medicine and Medical Specialties (DiMI), School of Medicine, University of Genoa, 16126 Genoa, Italy.
U.O. Clinica di Oncologia Medica, IRCCS Ospedale Policlinico San Martino, 16132 Genoa, Italy.
Cancers (Basel). 2025 Feb 14;17(4):652. doi: 10.3390/cancers17040652.
: Approximately 25-30% of non-small-cell lung cancer (NSCLC) patients are diagnosed when the disease is still resectable, although the risk of recurrence is significant. Recently, approaches based on targeted agents or immune checkpoint inhibitors (ICIs) have modified the management of such patients. However, some questions remain unanswered. : Our aim is to assess the current evidence on approaches involving targeted agents and ICIs in resectable NSCLC, to provide an up-to-date overview of the subject, and to identify areas of current debate, : We analyzed randomized trials on ICIs and targeted therapies in early-stage NSCLC, published or presented at international oncology meetings throughout the last 5 years. : Osimertinib and alectinib have shown robust results in the adjuvant setting for molecularly identified patient subgroups, while ICIs have achieved robust data in the neoadjuvant/perioperative setting, with less consistent data on the pure adjuvant approach. Circulating tumor DNA levels may offer a possible biomarker for therapeutic decisions, albeit more prospective data are needed. : Targeted agents and ICIs are revolutionizing early-stage NSCLC, similarly to what was observed in advanced disease. Prospective studies designed to compare neoadjuvant, adjuvant, and perioperative approaches and to assess the role of circulating biomarkers are warranted.
大约25%至30%的非小细胞肺癌(NSCLC)患者在疾病仍可切除时被诊断出来,尽管复发风险很大。最近,基于靶向药物或免疫检查点抑制剂(ICI)的方法改变了此类患者的治疗方式。然而,一些问题仍未得到解答。我们的目的是评估目前关于可切除NSCLC中涉及靶向药物和ICI的方法的证据,提供该主题的最新概述,并确定当前存在争议的领域。我们分析了过去5年在国际肿瘤学会议上发表或展示的关于早期NSCLC中ICI和靶向治疗的随机试验。奥希替尼和阿来替尼在分子鉴定的患者亚组的辅助治疗中显示出强劲的结果,而ICI在新辅助/围手术期治疗中取得了可靠的数据,在单纯辅助治疗方法上的数据则不太一致。循环肿瘤DNA水平可能为治疗决策提供一种可能的生物标志物,尽管还需要更多的前瞻性数据。靶向药物和ICI正在彻底改变早期NSCLC的治疗,类似于在晚期疾病中观察到的情况。有必要开展前瞻性研究,以比较新辅助、辅助和围手术期治疗方法,并评估循环生物标志物的作用。