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贝伐珠单抗:一种叙述性药物评价。

Belzutifan: A Narrative Drug Review.

机构信息

Department of Medical Oncology, Amrita Institute of Medical Sciences and Research Centre, Amrita Vishwa Vidyapeetham, Kochi, Kerala, India, 682041.

出版信息

Curr Drug Res Rev. 2022;14(2):88-95. doi: 10.2174/2589977514666220401094724.

Abstract

Von Hippel-Lindau disease is an autosomal dominant disorder characterised by renal cell carcinomas, pancreatic neuroendocrine tumours, central nervous system hemangioblastomas, retinoblastomas, and tumours of the reproductive tract. This disease results from loss of function mutations in the tumour suppressor gene known as the Von Hippel-Lindau gene, located on chromosome 3. Loss of function mutation in the Von Hippel-Lindau gene results in the accumulation of a protein known as a hypoxia-inducible factor, which promotes cellular proliferation and angiogenesis, leading to cancer. Belzutifan inhibits the hypoxia-inducible factor by binding to the Per-ARNT -Sim-B binding pocket on the hypoxia-inducible factor -2α, inhibiting cellular proliferation and angiogenesis. In our thorough literature review, we identified 37 relevant articles. Belzutifan showed clinically meaningful response rates for both Von Hippel-Lindau disease-associated renal cell carcinomas and non-renal cell cancers. The pharmacokinetic profile of belzutifan was much better than its congener molecules due to the optimisation of its dihalide groups from germinal to vicinal. The pharmacodynamic effect of belzutifan was confirmed by its ability to decrease serum erythropoietin, which is a direct result of hypoxia-inducible factor- 2α inhibition. The significant side effects observed were anaemia, hypoxia, fatigue, hypertension, visual impairment and weight gain. Multiple clinical trials are currently underway to determine the role of beluztifan as part of combination regimens in treating Von Hippel-Lindau diseaseassociated malignancies.

摘要

希佩尔-林道病是一种常染色体显性遗传疾病,其特征是肾细胞癌、胰腺神经内分泌肿瘤、中枢神经系统血管母细胞瘤、视网膜母细胞瘤和生殖系统肿瘤。这种疾病是由于肿瘤抑制基因希佩尔-林道基因的功能丧失突变引起的,该基因位于 3 号染色体上。希佩尔-林道基因的功能丧失突变导致一种称为缺氧诱导因子的蛋白质积累,从而促进细胞增殖和血管生成,导致癌症。贝伐单抗通过与缺氧诱导因子-2α上的 Per-ARNT-Sim-B 结合口袋结合来抑制缺氧诱导因子,从而抑制细胞增殖和血管生成。在我们全面的文献综述中,我们确定了 37 篇相关文章。贝伐单抗在希佩尔-林道病相关肾细胞癌和非肾细胞癌中均显示出有临床意义的反应率。贝伐单抗的药代动力学特征由于其二卤代物从生殖位优化为顺位,因此明显优于其同类分子。贝伐单抗的药效学作用通过其降低血清促红细胞生成素的能力得到证实,这是缺氧诱导因子-2α抑制的直接结果。观察到的显著副作用包括贫血、缺氧、疲劳、高血压、视力障碍和体重增加。目前正在进行多项临床试验,以确定贝伐单抗作为治疗希佩尔-林道病相关恶性肿瘤联合治疗方案一部分的作用。

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