A narrative review on perioperative systemic therapy in non-small cell lung cancer

R. Hsu, Z. Arter, Darin Poei, D.J. Benjamin
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Abstract

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 EGFR-mutated NSCLC and adjuvant alectinib in ALK-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.
非小细胞肺癌围手术期系统疗法综述
可手术的非小细胞肺癌(NSCLC)仍有很高的复发风险,在所有可手术病例中,尽管增加了辅助化疗,复发率仍接近 50%。然而,免疫疗法和靶向疗法的应用已超越了转移性非小细胞肺癌的范畴,进入了早期围手术期管理,这激发了巨大的热情,并改变了实践。NSCLC 阿特珠单抗辅助治疗首先证明了免疫检查点抑制剂的临床获益。随后,有研究表明,术前接受免疫疗法治疗的手术患者与仅接受化疗的患者相比,在主要病理反应方面获益显著,因此对新辅助 nivolumab 和化疗进行了评估,结果显示无事件生存期获益显著,从而引发了对围术期免疫疗法和化疗进行评估的后续研究。与此同时,在靶向疗法方面,表皮生长因子受体突变 NSCLC 的奥希替尼辅助疗法和 ALK 重组 NSCLC 的阿来替尼辅助疗法在临床试验中显示出临床获益后,均获得了监管部门的批准。随着该领域的快速发展变化,多种免疫疗法药物和抗体药物共轭物等新的组合药物正在开发中,NSCLC 的围手术期管理迅速变得复杂起来,围手术期治疗的途径也各不相同。此外,循环肿瘤 DNA 和有关免疫疗法反应预后的更好工具的研究将有助于决定哪些患者应该接受免疫疗法,如果是的话,应该在术前还是术前和术后都接受免疫疗法。在这篇综述中,我们回顾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过程,并展望了围手术期靶向治疗的未来。
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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