医学
神经内分泌肿瘤
无症状的
疾病
癌症研究
内科学
缺氧(环境)
胰腺癌
进行性疾病
肿瘤科
病理
癌症
有机化学
化学
氧气
作者
Eleonora Pellè,Taymeyah Al‐Toubah,Brian Morse,Jonathan R. Strosberg
出处
期刊:PubMed
日期:2022-12-01
卷期号:20 (12): 1285-1287
被引量:2
标识
DOI:10.6004/jnccn.2022.7047
摘要
von Hippel-Lindau (VHL) disease is a rare autosomal-dominant hereditary disease characterized by mutation of the VHL gene. This gene encodes for the VHL protein, which regulates the activity of HIF-α, a transcription factor involved in the cellular response to hypoxia. Mutations in VHL lead to the accumulation of HIF-α and, consequently, the engagement of hypoxia-sensitive genes with tumorigenic effects. VHL disease is associated with the development of tumors in multiple organs, including pancreatic neuroendocrine tumors (pNETs). Belzutifan is an HIF-α inhibitor; however, it has not been previously evaluated in patients with metastatic or treatment-refractory pNETs. This report presents a 43-year-old woman with VHL-associated metastatic pNET treated with belzutifan after progression on multiple systemic therapies. She began treatment with belzutifan and experienced partial radiographic response within 1 month of treatment. Other than asymptomatic anemia, no adverse effects developed during 5 months of ongoing therapy. Belzutifan is an inhibitor of HIF-2α that targets the underlying pathophysiology of VHL-associated pNETs. Our case report describes exceptional activity in a metastatic pNET arising from VHL.
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