Hsu Robert, Arter Zhaohui Liao, Poei Darin, Benjamin David J
Division of Medical Oncology, University of Southern California Norris Comprehensive Cancer Center, University of Southern California Keck School of Medicine, Los Angeles, CA 90033, USA.
Department of Medicine, Division of Hematology-Oncology, University of California Irvine School of Medicine, Orange, CA 92697, USA.
Explor Target Antitumor Ther. 2024;5(4):931-954. doi: 10.37349/etat.2024.00256. Epub 2024 Jul 26.
Non-small cell lung cancer (NSCLC) that is operable still carries a high risk of recurrence, approaching 50% of all operable cases despite adding adjuvant chemotherapy. However, the utilization of immunotherapy and targeted therapy moving beyond the metastatic NSCLC setting and into early-stage perioperative management has generated tremendous enthusiasm and has been practice-changing. Adjuvant atezolizumab in NSCLC first demonstrated a clinical benefit with an immune checkpoint inhibitor. Then, with studies studying a significant benefit in major pathologic response in surgical patients treated preoperatively with immunotherapy compared to only chemotherapy, neoadjuvant nivolumab and chemotherapy were evaluated and showed significant event-free survival benefit leading to subsequent studies evaluating perioperative immunotherapy and chemotherapy. Meanwhile, with regards to targeted therapies, adjuvant osimertinib in -mutated NSCLC and adjuvant alectinib in -rearranged NSCLC have both received regulatory approvals following demonstrated clinical benefit in clinical trials. With rapidly evolving changes in the field, new combinations such as multiple immunotherapy agents and antibody-drug conjugates in development, perioperative NSCLC management has quickly become complicated with different pathways to perioperative treatment. Furthermore, circulating tumor DNA and studies looking at better tools to prognosticate immunotherapy response will help with decision-making regarding which patients should receive immunotherapy and if so, either only pre-operatively or both pre- and post-operatively. In this review, we look at the evolution of systemic therapy in the perioperative setting from adjuvant chemotherapy to adjuvant immunotherapy to perioperative immunotherapy and look at perioperative targeted therapy while looking ahead to future considerations.
可手术切除的非小细胞肺癌(NSCLC)仍具有较高的复发风险,尽管增加了辅助化疗,所有可手术病例的复发风险仍接近50%。然而,免疫疗法和靶向疗法从转移性NSCLC领域扩展到早期围手术期管理,引发了极大的热情,并改变了临床实践。NSCLC中的辅助阿替利珠单抗首次证明了免疫检查点抑制剂的临床益处。随后,与仅接受化疗相比,研究显示术前接受免疫疗法治疗的手术患者在主要病理反应方面有显著益处,因此对新辅助纳武利尤单抗和化疗进行了评估,结果显示无事件生存有显著益处,从而促使后续研究评估围手术期免疫疗法和化疗。同时,关于靶向疗法,在临床试验中证明有临床益处后,针对表皮生长因子受体(EGFR)突变的NSCLC的辅助奥希替尼和针对间变性淋巴瘤激酶(ALK)重排的NSCLC的辅助阿来替尼均已获得监管批准。随着该领域的快速发展变化,多种免疫治疗药物和抗体药物偶联物等新组合正在研发中,围手术期NSCLC的管理因不同的围手术期治疗途径而迅速变得复杂。此外,循环肿瘤DNA以及寻找更好的预测免疫治疗反应工具的研究,将有助于决定哪些患者应接受免疫治疗,如果接受,是仅在术前还是术前和术后都接受。在本综述中,我们探讨了围手术期全身治疗从辅助化疗到辅助免疫治疗再到围手术期免疫治疗的演变,并展望未来的考虑因素,同时探讨围手术期靶向治疗。