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Drugs. 2020 Nov;80(17):1865-1870. doi: 10.1007/s40265-020-01427-4.
Pralsetinib (GAVRETO™, Blueprint Medicines Corporation) is a selective rearranged during transfection (RET) inhibitor being developed for the treatment of various solid tumours. RET is a well described proto-oncogene present in multiple cancers including non-small cell lung cancer (NSCLC), papillary thyroid cancer, and medullary thyroid carcinoma (MTC). Pralsetinib was recently granted accelerated approval for the treatment of metastatic RET fusion-positive NSCLC in the USA and is under regulatory review in the USA for RET fusion-positive thyroid cancer and RET mutation-positive MTC; pralsetinib is under regulatory review in the EU for RET fusion-positive NSCLC. This article summarizes the milestones in the development of pralsetinib leading to this first approval.
普拉替尼(GAVRETO™,Blueprint Medicines 公司)是一种选择性转染重排(RET)抑制剂,正在开发用于治疗各种实体肿瘤。RET 是一种在多种癌症中都有描述的原癌基因,包括非小细胞肺癌(NSCLC)、甲状腺乳头状癌和甲状腺髓样癌(MTC)。普拉替尼最近在美国获得了治疗转移性 RET 融合阳性 NSCLC 的加速批准,正在美国接受 RET 融合阳性甲状腺癌和 RET 突变阳性 MTC 的监管审查;普拉替尼正在欧盟接受 RET 融合阳性 NSCLC 的监管审查。本文总结了普拉替尼开发过程中的重要里程碑,最终促成了这一首次批准。