Department of Pulmonary Oncology, AORN dei Colli Monaldi, 80131 Naples, Italy.
Department of Precision Medicine, University of Campania "Luigi Vanvitelli", 80138 Naples, Italy.
Int J Mol Sci. 2023 Jan 26;24(3):2433. doi: 10.3390/ijms24032433.
RET-selective tyrosine kinase inhibitors (TKIs) selpercatinib and pralsetinib have revolutionized the landscape of RET-positive (RET+) advanced non-small cell lung cancer (NSCLC) treatment, thanks to their efficacy and safety profiles. This class of medications currently represents the standard of care for both naïve and patients that have not received selective RET-TKIs in the first-line setting. However, we presently lack a satisfactory understanding of resistance mechanism developing after selective RET-TKIs usage, as well as a specific treatment for patients progressing on selpercatinib or pralsetinib. Chemotherapy ± immunotherapy is considered as a recommended subsequent second-line regimen in these patients. Therefore, it is of paramount importance to better define and understand the resistance mechanisms triggered by RET-TKIs. With this in mind, the present review article has been conceived to provide a comprehensive overview about RET+ advanced NSCLC, both from a therapeutic and molecular point of view. Besides comparing the clinical outcome achieved in RET+ advanced NSCLC patients after multikinase inhibitors (MKIs) and/or RET-selective TKIs' administration, we focused on the molecular mechanisms accountable for their long-term resistance. Finally, a critical perspective on many of today's most debated issues and concerns is provided, with the purpose of shaping the possible pharmacological approaches for tomorrow's therapies.
RET 选择性酪氨酸激酶抑制剂 (TKI) 塞尔帕替尼和普拉替尼彻底改变了 RET 阳性 (RET+) 晚期非小细胞肺癌 (NSCLC) 的治疗格局,这要归功于它们的疗效和安全性。该类药物目前是初治和一线未接受选择性 RET-TKI 治疗的患者的标准治疗方法。然而,我们目前对选择性 RET-TKI 应用后耐药机制的了解还不够满意,也没有针对接受塞尔帕替尼或普拉替尼治疗后进展的患者的特定治疗方法。化疗±免疫治疗被认为是这些患者的二线推荐方案。因此,更好地定义和理解 RET-TKI 引发的耐药机制至关重要。有鉴于此,本文旨在从治疗和分子角度对 RET+晚期 NSCLC 进行全面概述。除了比较多激酶抑制剂 (MKIs) 和/或 RET 选择性 TKI 治疗后 RET+晚期 NSCLC 患者的临床结果外,我们还重点关注了导致其长期耐药的分子机制。最后,对当今许多备受争议的问题和关注点进行了批判性的探讨,以期为未来的治疗方法制定可能的药物治疗方法。