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Durvalumab: First Global Approval

机译:Durvalumab:第一个全球批准

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摘要

Intravenous durvalumab (Imfinzi (TM); 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 platinumcontaining 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.
机译:静脉内Durvalumab(Imfinzi(TM); Astrazeneca)是一种完全人单克隆抗体,其阻断编程的细胞死亡配体-1与其受体(PD-1和CD80)结合,导致增强针对癌细胞的T细胞应答。 美国FDA已授予Durvalumab加速批准用于治疗含有疾病进展期间或之后的血压癌化疗,或在Neoadjuvant或含辅助铂的化疗的12个月内进行疾病进展的患者。 Durvalumab +/- Tremelimumab是尿路上皮癌,非小细胞肺癌,小细胞肺癌和头部鳞状细胞癌的III期临床试验。 该药物也在各种固体肿瘤和血液恶性肿瘤中的II或II期临床试验中评估。 本文总结了Durvalumab发展的里程碑,导致这对尿路上皮癌的第一次批准。

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