Management of Adverse Events Associated with MET TKIs in Patients with Advanced NSCLC: A Podcast Discussion.

IF 5.1 3区 医学 Q2 ONCOLOGY
Targeted Oncology Pub Date : 2026-09-01 Epub Date: 2026-09-12 DOI:10.1007/s11523-026-01242-z
Wade T Iams, Narjust Florez
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引用次数: 0

Abstract

MET exon 14 (METex14) skipping is observed in approximately 3-4% of patients with non-small-cell lung cancer (NSCLC). These patients are typically older and may or may not have a history of tobacco use. Several small molecule MET tyrosine kinase inhibitors (TKIs) have been developed, showing clinical efficacy in trials targeting the MET pathway in these patients. Among these MET TKIs, tepotinib and capmatinib are globally approved and have demonstrated robust and durable efficacy in patients with METex14 skipping NSCLC in the VISION and GEOMETRY mono-1 trials. While MET TKIs have provided an important therapeutic option for patients with METex14 skipping NSCLC, they are associated with some challenging treatment-related adverse events (TRAEs). Across studies investigating MET TKIs, peripheral edema (49-68%) was reported as the most frequently observed TRAE and is widely recognized as a class effect of MET TKIs in patients with METex14 skipping NSCLC. Nausea (23-44%) and blood creatinine increase (22-34%) were other commonly reported TRAEs observed with treatments in this class. Effective treatment with MET TKIs relies on early recognition of AEs, regular monitoring, patient and caregiver education, and tailored supportive care interventions to ensure treatment continuity and optimal outcomes. Dose reductions have proven effective in mitigating AEs while preserving efficacy, by allowing patients to continue to receive efficacious targeted therapy. In this podcast article, the authors will discuss safety considerations with MET TKI treatment for patients with METex14 skipping NSCLC. They will also share their perspectives on the current landscape of MET TKIs in METex14 skipping NSCLC, commonly reported TRAEs in clinical practice, management strategies for these TRAEs, and safety considerations when switching one MET TKI to another. In addition, authors will discuss two patient cases to illustrate effective management of TRAEs associated with MET TKIs in patients with METex14 skipping NSCLC.

晚期NSCLC患者MET TKIs相关不良事件的管理:播客讨论
MET外显子14 (METex14)在约3-4%的非小细胞肺癌(NSCLC)患者中观察到跳跃。这些患者通常年龄较大,可能有也可能没有烟草使用史。几种小分子MET酪氨酸激酶抑制剂(TKIs)已经开发出来,在针对这些患者的MET途径的试验中显示出临床疗效。在这些MET TKIs中,替波替尼和卡马替尼已获得全球批准,并在VISION和GEOMETRY单-1试验中对METex14跳过NSCLC患者显示出稳健和持久的疗效。虽然MET TKIs为不使用METex14的非小细胞肺癌患者提供了重要的治疗选择,但它们与一些具有挑战性的治疗相关不良事件(TRAEs)相关。在研究MET TKIs的研究中,外周水肿(49% -68%)被报道为最常见的TRAE,并且被广泛认为是MET TKIs在METex14跳过NSCLC患者中的一类效应。恶心(23-44%)和血肌酐升高(22-34%)是这类治疗中常见的trae。MET TKIs的有效治疗依赖于ae的早期识别、定期监测、患者和护理人员教育以及量身定制的支持性护理干预措施,以确保治疗的连续性和最佳结果。减少剂量已被证明可有效减轻不良反应,同时保持疗效,允许患者继续接受有效的靶向治疗。在这篇播客文章中,作者将讨论MET TKI治疗METex14跳过NSCLC患者的安全性问题。他们还将分享他们对MET TKI在METex14跳过非小细胞肺癌中的现状、临床实践中常见的trae、这些trae的管理策略以及转换MET TKI时的安全性考虑的观点。此外,作者将讨论两个患者病例,以说明METex14跳过NSCLC患者与MET TKIs相关的trae的有效管理。
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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来源期刊
Targeted Oncology
Targeted Oncology 医学-肿瘤学
CiteScore
8.40
自引率
3.70%
发文量
64
审稿时长
>12 weeks
期刊介绍: Targeted Oncology addresses physicians and scientists committed to oncology and cancer research by providing a programme of articles on molecularly targeted pharmacotherapy in oncology. The journal includes: Original Research Articles on all aspects of molecularly targeted agents for the treatment of cancer, including immune checkpoint inhibitors and related approaches. Comprehensive narrative Review Articles and shorter Leading Articles discussing relevant clinically established as well as emerging agents and pathways. Current Opinion articles that place interesting areas in perspective. Therapy in Practice articles that provide a guide to the optimum management of a condition and highlight practical, clinically relevant considerations and recommendations. Systematic Reviews that use explicit, systematic methods as outlined by the PRISMA statement. Adis Drug Reviews of the properties and place in therapy of both newer and established targeted drugs in oncology.
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