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早期非小细胞肺癌患者的辅助免疫治疗及未来方向。

Adjuvant Immunotherapy in Patients with Early-Stage Non-small Cell Lung Cancer and Future Directions.

机构信息

Division of Medical Oncology, National Cancer Centre Singapore, 11 Hospital Crescent, Singapore, 169610, Singapore.

SingHealth Duke-NUS Oncology Academic Clinical Programme, 11 Hospital Crescent, Singapore, 169610, Singapore.

出版信息

Curr Treat Options Oncol. 2022 Dec;23(12):1721-1731. doi: 10.1007/s11864-022-01034-3. Epub 2022 Dec 1.

Abstract

While cisplatin-based adjuvant chemotherapy has been the standard of care for the past two decades, the recent introduction of immunotherapy has heralded an important milestone in the adjuvant landscape of early-stage non-small cell lung cancer (NSCLC). The landmark approval of adjuvant atezolizumab based on disease-free survival (DFS) benefit in IMpower010 was swiftly followed by the recent data for use of adjuvant pembrolizumab in PEARLS/KEYNOTE-091, and similar trials involving other immune checkpoint inhibitors are eagerly anticipated. Although both atezolizumab and pembrolizumab demonstrated a significant DFS benefit in the intention-to-treat population, key subgroup analyses have raised questions about the role of predictive biomarkers such as PD-L1 expression and EGFR-mutation status. In this review, we examine the data from the two important trials (IMpower010 and PEARLS/KEYNOTE-091), discuss the controversies surrounding adjuvant immunotherapy including appropriate endpoints, biomarker selection and highlight key considerations in oncogene-driven NSCLC. Finally, we propose future directions including the impact of neoadjuvant therapy on developments in the adjuvant immunotherapy paradigm and role of minimal residual disease (MRD).

摘要

在过去的二十年中,顺铂为基础的辅助化疗一直是标准的治疗方法,但最近免疫疗法的引入标志着早期非小细胞肺癌(NSCLC)辅助治疗领域的一个重要里程碑。基于无病生存期(DFS)获益的 IMpower010 研究中辅助阿替利珠单抗的里程碑式批准,随后迅速跟进了近期辅助帕博利珠单抗在 PEARLS/KEYNOTE-091 中的数据,以及其他涉及免疫检查点抑制剂的类似试验也备受期待。虽然阿替利珠单抗和帕博利珠单抗在意向治疗人群中均显示出显著的 DFS 获益,但关键亚组分析对预测生物标志物(如 PD-L1 表达和 EGFR 突变状态)的作用提出了质疑。在这篇综述中,我们检查了来自两项重要试验(IMpower010 和 PEARLS/KEYNOTE-091)的数据,讨论了辅助免疫治疗的争议,包括适当的终点、生物标志物选择以及强调驱动基因 NSCLC 的关键考虑因素。最后,我们提出了未来的方向,包括新辅助治疗对辅助免疫治疗范式发展的影响以及微小残留病(MRD)的作用。

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