Targeted therapy with anlotinib for a H3K27M mutation diffuse midline glioma patient with PDGFR-α mutation: a case report

Acta Neurochir (Wien). 2022 Aug;164(8):2063-2066. doi: 10.1007/s00701-021-05061-1. Epub 2021 Nov 23.

Abstract

H3K27M-mutant diffuse midline glioma (H3K27M-mt DMG) was a novel entity, which was defined by K27M mutations in H3F3A or HIST1H3B/C in the 2016 WHO updated fourth edition of the central nervous system (CNS) tumor classification. There is an urgent need for effective therapeutic strategies. Anlotinib is a multitarget tyrosine kinase inhibitor, which has not been reported for H3K27M-mt DMG treatment. Here, we firstly reported an adult multifocal H3K27M-mt DMG patient benefiting from anlotinib. This report provides a promising treatment option for H3K27M-mt DMG patients.

Keywords: Anlotinib; Diffuse midline gliomas; H3K27M mutation; Multitarget tyrosine kinase inhibitor.

Publication types

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

MeSH terms

  • Adult
  • Brain Neoplasms* / drug therapy
  • Brain Neoplasms* / genetics
  • Glioma* / drug therapy
  • Glioma* / genetics
  • Histones* / genetics
  • Humans
  • Indoles* / therapeutic use
  • Molecular Targeted Therapy
  • Mutation*
  • Protein-Tyrosine Kinases / antagonists & inhibitors
  • Quinolines* / therapeutic use
  • Receptor, Platelet-Derived Growth Factor alpha* / genetics

Substances

  • Histones
  • Indoles
  • Quinolines
  • anlotinib
  • Protein-Tyrosine Kinases
  • Receptor, Platelet-Derived Growth Factor alpha