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靶向缺氧诱导因子-2α:贝佐替凡在透明细胞肾细胞癌治疗中的作用

Targeting HIF-2α: the role of belzutifan in clear cell renal carcinoma management.

作者信息

Valdés Alejandro, Pizarro Gonzalo, González-Montero Jaime, Rojas Carlos, Burotto Mauricio

机构信息

Department of Medical Oncology, Bradford Hill Clinical Research Center, Santiago, Chile.

Department of Medical Oncology, Instituto Nacional del Cáncer, Santiago, Chile.

出版信息

Expert Rev Clin Pharmacol. 2025 Jan-Feb;18(1-2):17-27. doi: 10.1080/17512433.2024.2436433. Epub 2024 Dec 13.

DOI:10.1080/17512433.2024.2436433
PMID:39670660
Abstract

INTRODUCTION

Belzutifan is a first-in-class hypoxia-inducible factor-2 alpha (HIF-2α) inhibitor. It targets the von Hippel-Lindau protein (pVHL)-HIF-vascular endothelial growth factor (VEGF) pathway, which is crucial in cellular responses to hypoxia. By inhibiting HIF-2α, belzutifan disrupts the transcription of genes involved in tumor growth and angiogenesis.

AREAS COVERED

In this review, we describe the pVHL-HIF-VEGF pathway and how it led to the development of HIF inhibitors, including belzutifan. A search was conducted for trials involving Belzutifan, including phase I-III trials. We describe the relevant toxicity, with emphasis on hypoxia and anemia.

EXPERT OPINION

Belzutifan is a relatively safe drug, with manageable adverse events, including anemia and hypoxia as on-target toxicity. Ongoing trials are studying its benefit in overall survival for RCC in first-line treatment and its potential in other malignancies. The LITESPARK-005 trial reported the benefit of belzutifan in progression-free survival (PFS) compared to everolimus in later lines of treatment, with improvement in quality-of-life outcomes. Given its different mechanism of action to currently available treatments, belzutifan is expected to play a prominent role in the treatment of clear cell renal carcinoma and other cancers.

摘要

简介

贝佐替凡(Belzutifan)是首个同类的缺氧诱导因子-2α(HIF-2α)抑制剂。它作用于希佩尔-林道蛋白(pVHL)-HIF-血管内皮生长因子(VEGF)通路,该通路在细胞对缺氧的反应中起关键作用。通过抑制HIF-2α,贝佐替凡破坏参与肿瘤生长和血管生成的基因转录。

涵盖领域

在本综述中,我们描述了pVHL-HIF-VEGF通路以及它如何促成了包括贝佐替凡在内的HIF抑制剂的研发。我们检索了涉及贝佐替凡的试验,包括I-III期试验。我们描述了相关毒性,重点是缺氧和贫血。

专家观点

贝佐替凡是一种相对安全的药物,不良事件可控,包括贫血和缺氧作为靶向毒性。正在进行的试验正在研究其在一线治疗中对肾细胞癌总生存期的益处以及在其他恶性肿瘤中的潜力。LITESPARK-005试验报告了与依维莫司相比,贝佐替凡在后续治疗线中对无进展生存期(PFS)的益处,以及生活质量结果的改善。鉴于其与现有治疗方法不同的作用机制,贝佐替凡有望在透明细胞肾细胞癌和其他癌症的治疗中发挥重要作用。

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