Early molecular diagnosis of BRAF status drives the neurosurgical management in BRAF V600E-mutant pediatric low-grade gliomas: a case report

BMC Pediatr. 2022 Nov 29;22(1):685. doi: 10.1186/s12887-022-03711-6.

Abstract

Background: To date, this is the only report showing with close and consecutive magnetic resonance images the extremely rapid response of two types of pediatric low-grade gliomas (PLGG) to vemurafenib and its impact on the surgical approach.

Cases presentation: We report two cases of symptomatic PLGG treated with vemurafenib, a BRAF inhibitor: in a 12-year-old girl it was used as first-line medical treatment, reducing the tumor by 45% within a month and stabilizing to 76% after a year; in a 3-year-old boy with no improvement after SIOP LGG 2004 Protocol, vemurafenib induced in only one week a 34% shrinkage and solved the hydrocephalus, avoiding surgical operation. DISCUSSION AND CONCLUSIONS: Our cases demonstrate how an early molecular diagnosis of BRAF mutations through the neurosurgical biopsy is essential to promptly start targeted therapies., whose effect can influence both therapeutic and surgical decisions, hopefully reducing the occurrence of second neurosurgery with associated risks of neurological sequelae.

Keywords: BRAF; Brain tumors; Case report; Neurosurgery; Vemurafenib.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biopsy
  • Child
  • Child, Preschool
  • Early Diagnosis
  • Female
  • Glioma* / drug therapy
  • Glioma* / genetics
  • Glioma* / surgery
  • Humans
  • Male
  • Proto-Oncogene Proteins B-raf* / genetics
  • Vemurafenib / therapeutic use

Substances

  • Proto-Oncogene Proteins B-raf
  • Vemurafenib
  • BRAF protein, human