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色瑞替尼:首次批准。

Selumetinib: First Approval.

机构信息

Springer Nature, Private Bag 65901, Mairangi Bay, Auckland, 0754, New Zealand.

出版信息

Drugs. 2020 Jun;80(9):931-937. doi: 10.1007/s40265-020-01331-x.

Abstract

Selumetinib (KOSELUGO; AZD6244, ARRY-142886) is a mitogen-activated protein kinase 1 and 2 (MEK1/2) inhibitor being developed by AstraZeneca for the treatment of tumours associated with neurofibromatosis and various cancers. Selumetinib has been granted orphan drug status as adjuvant treatment for thyroid cancer (in the USA) and as treatment for neurofibromatosis type 1 (in the USA and the EU) and, based on the results of the phase II SPRINT trial, was recently approved in the USA in paediatric patients with neurofibromatosis type 1 and symptomatic, inoperable plexiform neurofibromas. This article summarizes the milestones in the development of selumetinib leading to this first approval for the treatment of paediatric patients aged ≥ 2 years with neurofibromatosis type 1 who have symptomatic, inoperable plexiform neurofibromas.

摘要

司美替尼(KOSELUGO;AZD6244,ARRY-142886)是一种丝裂原活化蛋白激酶 1 和 2(MEK1/2)抑制剂,由阿斯利康公司开发,用于治疗与神经纤维瘤病和各种癌症相关的肿瘤。司美替尼已被授予孤儿药地位,作为甲状腺癌的辅助治疗(在美国)和神经纤维瘤病 1 型的治疗(在美国和欧盟),并且基于 II 期 SPRINT 试验的结果,最近在美国批准用于治疗 2 岁及以上患有神经纤维瘤病 1 型且伴有症状性、不可手术性丛状神经纤维瘤的儿科患者。本文总结了司美替尼开发过程中的重要里程碑,从而首次批准用于治疗 2 岁及以上患有神经纤维瘤病 1 型且伴有症状性、不可手术性丛状神经纤维瘤的儿科患者。

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