Cortot Alexis, Le Xiuning, Smit Egbert, Viteri Santiago, Kato Terufumi, Sakai Hiroshi, Park Keunchil, Camidge D Ross, Berghoff Karin, Vlassak Soetkin, Paik Paul K
Université de Lille, CHU Lille, Thoracic Oncology Department, Centre National de la Recherche Scientifique, INSERM, Institut Pasteur de Lille, UMR9020-UMR-S 1277-Canther, Lille, France.
M.D. Anderson Cancer Center, University of Texas, Houston, TX.
Clin Lung Cancer. 2022 May;23(3):195-207. doi: 10.1016/j.cllc.2022.01.003. Epub 2022 Feb 4.
MET exon 14 (METex14) skipping mutations occur in 3% to 4% of non-small cell lung cancer (NSCLC) cases. Currently, four oral MET tyrosine kinase inhibitors (TKIs) are in use for the treatment of patients with METex14 skipping NSCLC (tepotinib, capmatinib, savolitinib, and crizotinib). To support optimal management of METex14 skipping NSCLC in this typically older patient population, the safety profiles of these treatment options are reviewed here. Published safety data from prospective clinical trials with MET TKIs in patients with METex14 skipping NSCLC were reviewed. Treatment-related adverse events (TRAEs) occurring in ≥ 10% of patients were reported where feasible. Guidance on clinical monitoring and management of key MET TKI TRAEs and drug-drug interactions is provided. Across the clinical trials, safety data for MET TKIs were reported for 442 patients with METex14 skipping. Peripheral edema was the most reported TRAE (50%-63% of patients; grade ≥ 3: 1%-11%), followed by nausea (26%-46% of patients; grade ≥ 3: 0%-1%). TRAEs led to dose reductions in 33% to 38% of patients and to discontinuation in 7% to 14% of patients, across the MET TKIs. Considerations on interpreting available safety data are provided, along with insights into monitoring and managing specific MET TKI TRAEs of interest and drug-drug interactions. Overall, MET TKIs are tolerable treatment options for patients with METex14 skipping NSCLC, an older population for whom chemo- or immuno-therapy may not be an effective nor tolerable option. More data regarding the effectiveness of safety interventions and management strategies are needed.
MET外显子14(METex14)跳跃突变发生在3%至4%的非小细胞肺癌(NSCLC)病例中。目前,有四种口服MET酪氨酸激酶抑制剂(TKIs)用于治疗METex14跳跃型NSCLC患者(特泊替尼、卡马替尼、赛沃替尼和克唑替尼)。为了支持对这一典型老年患者群体中METex14跳跃型NSCLC的最佳管理,本文对这些治疗方案的安全性进行了综述。回顾了MET TKIs用于METex14跳跃型NSCLC患者的前瞻性临床试验的已发表安全性数据。在可行的情况下,报告了≥10%患者发生的与治疗相关的不良事件(TRAEs)。提供了关于关键MET TKI TRAEs的临床监测和管理以及药物相互作用的指导。在各项临床试验中,报告了442例METex14跳跃型患者使用MET TKIs的安全性数据。外周水肿是报告最多的TRAEs(50%-63%的患者;3级及以上:1%-11%),其次是恶心(26%-46%的患者;3级及以上:0%-1%)。在所有MET TKIs中,TRAEs导致33%至38%的患者剂量减少,7%至14%的患者停药。文中提供了对现有安全性数据的解读考量,以及对监测和管理特定MET TKI TRAEs及药物相互作用关注问题的见解。总体而言,MET TKIs对于METex14跳跃型NSCLC患者是可耐受的治疗选择,对于这一老年人群,化疗或免疫治疗可能既不是有效的也不是可耐受的选择。需要更多关于安全干预措施和管理策略有效性的数据。