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Drugs. 2021 Apr;81(6):697-708. doi: 10.1007/s40265-021-01503-3. Epub 2021 Apr 19.
Entrectinib (Rozlytrek) is an orally active, CNS-penetrant, small-molecule, selective inhibitor of the tropomyosin receptor tyrosine kinases TRKA/B/C [encoded by the neurotrophic tyrosine receptor kinase (NTRK) genes NTRK1/2/3, respectively], the proto-oncogene tyrosine-protein kinase ROS1 (ROS1) and the anaplastic lymphoma kinase gene (ALK). It is approved for the treatment of adults and paediatric patients aged ≥ 12 years with NTRK fusion-positive (NTRK+) solid tumours and adults with ROS1 fusion-positive (ROS1+) non-small-cell lung cancer (NSCLC). In trials in adults, entrectinib induced clinically meaningful and durable systemic responses in tyrosine kinase inhibitor (TKI)-naïve patients with locally-advanced or metastatic NTRK+ solid tumours or ROS1+ NSCLC, irrespective of the presence or absence of CNS metastases at baseline. Moreover, entrectinib demonstrated substantial intracranial efficacy in patients with baseline CNS metastases. Entrectinb efficacy in paediatric patients was established on the basis of extrapolation of clinical trial data from adults with NTRK+ solid tumours and children and adolescents aged < 21 years with recurrent or refractory NTRK+ CNS/solid tumours. Entrectinib was generally well tolerated, with a manageable safety profile. Thus, entrectinib expands the range of treatment options for advanced NTRK+ solid tumours and ROS1+ NSCLC, and may be of particular value in patients with existing CNS metastases and those who are at risk of developing CNS metastases.
恩曲替尼(Rozlytrek)是一种口服活性、可穿透中枢神经系统的小分子、选择性抑制剂,可抑制原肌球蛋白受体酪氨酸激酶 TRKA/B/C [分别由神经营养受体酪氨酸激酶(NTRK)基因 NTRK1/2/3 编码]、原癌基因酪氨酸蛋白激酶 ROS1(ROS1)和间变性淋巴瘤激酶基因(ALK)。它被批准用于治疗 12 岁及以上 NTRK 融合阳性(NTRK+)实体瘤和 ROS1 融合阳性(ROS1+)非小细胞肺癌(NSCLC)的成人和儿科患者。在成人试验中,恩曲替尼诱导了酪氨酸激酶抑制剂(TKI)初治的局部晚期或转移性 NTRK+实体瘤或 ROS1+ NSCLC 患者具有临床意义且持久的全身反应,无论基线时是否存在中枢神经系统转移。此外,恩曲替尼在基线存在中枢神经系统转移的患者中表现出显著的颅内疗效。在儿科患者中,恩曲替尼的疗效是基于对 NTRK+实体瘤的成人和年龄<21 岁的复发性或难治性 NTRK+中枢神经系统/实体肿瘤的儿童和青少年的临床试验数据进行外推而确立的。恩曲替尼总体耐受性良好,安全性可控。因此,恩曲替尼扩大了晚期 NTRK+实体瘤和 ROS1+ NSCLC 的治疗选择范围,对于存在中枢神经系统转移和有发生中枢神经系统转移风险的患者可能具有特别的价值。