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[免疫疗法治疗晚期或转移性黑色素瘤:纳武单抗从I期研究到获得欧洲药品管理局批准]

[Immunotherapy in the treatment of advanced or metastatic melanoma: nivolumab from phase I studies to approvement by European Medicines Agency].

作者信息

Queirolo Paola, Tanda Enrica Teresa

出版信息

Recenti Prog Med. 2015 Dec;106(12):608-17. doi: 10.1701/2094.22650.

Abstract

The treatment of advanced melanoma underwent a complete revolution over the last years. Targeted therapy and immunotherapy marked the beginning of a new management model for cancer. Targeted therapies are drugs directed exclusively against specific molecules in order to modulate their action. Immunotherapy, on the other hand, operates through drugs aimed to restoring the normal anti-tumor activity of the immune system. Indeed, in pathological conditions the immune system could be silenced or avoided through several mechanisms of "immunological escape". Since Food and Drug Administration (FDA) approval of ipilimumab in 2011, many other molecules have been investigated. Recently, anti-PD-1 (nivolumab and pembrolizumab) achieved promising results. The aim of this review is to trace the history of nivolumab, through major Phase I, II and III studies until FDA and European Medicines Agency approval.

摘要

在过去几年中,晚期黑色素瘤的治疗经历了彻底的变革。靶向治疗和免疫治疗标志着癌症新管理模式的开端。靶向治疗药物专门针对特定分子,以调节其作用。另一方面,免疫治疗则通过旨在恢复免疫系统正常抗肿瘤活性的药物发挥作用。实际上,在病理状态下,免疫系统可能会通过多种“免疫逃逸”机制被抑制或避开。自2011年美国食品药品监督管理局(FDA)批准伊匹木单抗以来,人们对许多其他分子进行了研究。最近,抗程序性死亡蛋白1(PD-1)药物(纳武单抗和帕博利珠单抗)取得了令人鼓舞的成果。本综述的目的是追溯纳武单抗的历史,涵盖主要的I期、II期和III期研究,直至其获得FDA和欧洲药品管理局的批准。

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