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转移性肾细胞癌中HIF-2α靶向治疗的新方法

Novel Approaches with HIF-2α Targeted Therapies in Metastatic Renal Cell Carcinoma.

作者信息

Nguyen Charles B, Oh Eugene, Bahar Piroz, Vaishampayan Ulka N, Else Tobias, Alva Ajjai S

机构信息

Rogel Comprehensive Cancer Center, University of Michigan, Ann Arbor, MI 48109, USA.

Division of Hematology and Oncology, Department of Internal Medicine, University of Michigan, Ann Arbor, MI 48109, USA.

出版信息

Cancers (Basel). 2024 Jan 31;16(3):601. doi: 10.3390/cancers16030601.

Abstract

Germline inactivation of the Von Hippel-Lindau () tumor suppressor is the defining hallmark in hereditary VHL disease and VHL-associated renal cell carcinoma (RCC). However, somatic mutations are also observed in patients with sporadic RCC. Loss of function mutations result in constitutive activation of hypoxia-inducible factor-2 alpha (HIF-2α), which leads to increased expression of HIF target genes that promote angiogenesis and tumor growth. As of 2023, belzutifan is currently the only approved HIF-2α inhibitor for both VHL-associated and sporadic metastatic RCC (mRCC). However, there is potential for resistance with HIF-2α inhibitors which warrants novel HIF-2α-targeting strategies. In this review, we discuss the potential resistance mechanisms with belzutifan and current clinical trials evaluating novel combinations of belzutifan with other targeted therapies and immune checkpoint inhibitors which may enhance the efficacy of HIF-2α targeting. Lastly, we also discuss newer generation HIF-2α inhibitors that are currently under early investigation and outline future directions and challenges with HIF-2α inhibitors for mRCC.

摘要

冯·希佩尔-林道(VHL)肿瘤抑制基因的种系失活是遗传性VHL病和VHL相关肾细胞癌(RCC)的决定性标志。然而,散发性RCC患者中也观察到体细胞突变。功能丧失性突变导致缺氧诱导因子-2α(HIF-2α)的组成性激活,这会导致促进血管生成和肿瘤生长的HIF靶基因表达增加。截至2023年,贝佐蒂凡(belzutifan)是目前唯一被批准用于VHL相关和散发性转移性RCC(mRCC)的HIF-2α抑制剂。然而,HIF-2α抑制剂存在耐药的可能性,这就需要新的HIF-2α靶向策略。在本综述中,我们讨论了贝佐蒂凡的潜在耐药机制,以及目前评估贝佐蒂凡与其他靶向治疗和免疫检查点抑制剂联合使用的临床试验,这些联合使用可能会提高HIF-2α靶向治疗的疗效。最后,我们还讨论了目前正在早期研究中的新一代HIF-2α抑制剂,并概述了mRCC的HIF-2α抑制剂的未来方向和挑战。

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