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度伐利尤单抗:全球首次获批。

Durvalumab: First Global Approval.

机构信息

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

出版信息

Drugs. 2017 Aug;77(12):1369-1376. doi: 10.1007/s40265-017-0782-5.

Abstract

Intravenous durvalumab (Imfinzi™; AstraZeneca) is a fully human monoclonal antibody that blocks programmed cell death ligand-1 binding to its receptors (PD-1 and CD80), resulting in enhanced T-cell responses against cancer cells. The US FDA has granted durvalumab accelerated approval for the treatment of patients with locally advanced or metastatic urothelial carcinoma who have disease progression during or following platinum-containing chemotherapy, or within 12 months of neoadjuvant or adjuvant platinum-containing chemotherapy. Durvalumab ± tremelimumab is under phase III clinical trials in urothelial carcinoma, non-small cell lung cancer, small cell lung cancer and head and neck squamous cell carcinoma. The drug is also being evaluated in phase I or II clinical trials in a wide range of solid tumours and haematological malignancies. This article summarizes the milestones in the development of durvalumab leading to this first approval for urothelial carcinoma.

摘要

静脉注射度伐鲁单抗(Imfinzi™;阿斯利康)是一种完全人源化单克隆抗体,可阻断程序性死亡配体-1与其受体(PD-1 和 CD80)的结合,从而增强 T 细胞对癌细胞的反应。美国 FDA 已批准度伐鲁单抗加速批准用于治疗局部晚期或转移性尿路上皮癌患者,这些患者在含铂化疗期间或之后、或在新辅助或辅助含铂化疗后 12 个月内出现疾病进展。度伐鲁单抗联合 Tremelimumab 正在进行尿路上皮癌、非小细胞肺癌、小细胞肺癌和头颈部鳞状细胞癌的 III 期临床试验。该药还在广泛的实体瘤和血液恶性肿瘤的 I 期或 II 期临床试验中进行评估。本文总结了度伐鲁单抗开发过程中的重要里程碑,这些里程碑促成了该药在尿路上皮癌的首次批准。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/052b/5636860/8cc1d73838ed/40265_2017_782_Figa_HTML.jpg

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