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Drugs. 2019 Feb;79(2):201-206. doi: 10.1007/s40265-018-1044-x.
Larotrectinib (VITRAKVI) is an orally administered, small molecule, highly-selective, tropomyosin receptor kinase (TRK) inhibitor that was developed by Loxo Oncology in collaboration with Bayer AG as a treatment for adult and paediatric patients whose cancers harbour neurotrophic receptor tyrosine kinase (NTRK) gene fusions. In November 2018 larotrectinib received its first global approval in the USA for the treatment of adult and paediatric patients with solid tumours that have a NTRK gene fusion without a known acquired resistance mutation, are metastatic or where surgical resection is likely to result in severe morbidity, and have no satisfactory alternative treatments or that have progressed following treatment. A registration application for the use of larotrectinib in paediatric and adult patients with locally advanced or metastatic solid tumours with NTRK gene fusion proteins has been submitted in the EU. This article summarizes the milestones in the development of larotrectinib leading to its first approval for the treatment of adult and paediatric patients with solid tumours that have NTRK gene fusion.
拉罗替尼(Vitrakvi)是一种口服小分子、高度选择性的原肌球蛋白受体激酶(TRK)抑制剂,由 Loxo Oncology 与 Bayer AG 合作开发,用于治疗成人和儿科患者,这些患者的癌症具有神经营养受体酪氨酸激酶(NTRK)基因融合。2018 年 11 月,拉罗替尼在美国首次获得全球批准,用于治疗具有 NTRK 基因融合而无已知获得性耐药突变、转移性或手术切除可能导致严重发病率的成人和儿科实体瘤患者,且无满意的替代治疗或在治疗后进展。拉罗替尼在欧盟的注册申请已提交用于治疗具有 NTRK 基因融合蛋白的局部晚期或转移性实体瘤的儿科和成年患者。本文总结了拉罗替尼开发过程中的重要里程碑,导致其首次批准用于治疗具有 NTRK 基因融合的成人和儿科实体瘤患者。