Pediatric patients with von Hippel–Lindau and hemangioblastomas treated successfully with belzutifan
Year: 2024
Type: article
Study design: Case Report
Abstract: Hemangioblastoma is the most common tumor associated with von Hippel-Lindau (VHL), and are a leading cause of mortality. We present five pediatric patients with VHL-associated hemangioblastomas treated with belzutifan, a hypoxia-inducible factor 2a (HIF2a) inhibitor. Three patients were started on belzutifan due to vision loss from progressive retinal hemangioblastomas. Within one year of treatment, all three patients had improvement in hemangioblastoma size and visual acuity. For patients with intracranial lesions, belzutifan resulted in an improvement in neurologic symptoms and hemangioblastoma size. Four patients experienced grade 1-2 anemia and two patients required a dose reduction. Our report suggests that belzutifan can be an effective therapy for pediatric, adolescent, and young adult patients with VHL-associated hemangioblastomas.
Source: Pediatric Blood & Cancer
DOI: 10.1002/pbc.31371
Authors: Emily Duan, Michael Robinson, Charles Davis, Sumit Pruthi, Christina Shin, Marisa Lewis, Julian A. Martinez‐Agosto, Michael B. Gorin, Brian M. Shuch, Debra L. Friedman, Vivian Y. Chang
Language: English
Topic: Ear and Head Tumors
Subfield: Oncology
Field: Medicine
Domain: Health Sciences
Open Access status: hybrid
Estimated APC paid: $4,550
OpenAlex ID: W4403501889
