Malignant meningioma mTOR mutated and precision medicine

Neurol Sci. 2023 Mar;44(3):1073-1075. doi: 10.1007/s10072-022-06575-x. Epub 2022 Dec 26.

Abstract

Background: WHO grade II and III meningiomas are more invasive than grade I malignancies and determine patients' shorter overall survival. Their tendency to recur after treatment has represented an important therapeutic challenge because of the limited treatment strategies at recurrence. Angiogenesis and mechanistic target of rapamycin (mTOR) activation are two of the main features of higher grade meningiomas, determining invasiveness and tendency to relapse. While these options prove promising, available clinical data on mTOR inhibitors' efficacy are somewhat limited.

Case study: We report a case of a 25-year-old female patient diagnosed with a right parasagittal occipital anaplastic meningioma (grade III WHO) in 2013. The patient underwent multiple treatments and, in 2019, a further recurrence occurred. The patient reported an mTOR mutation, and it is for this reason that the MTB approved treatment with everolimus and bevacizumab. Therapy was administered in May 2019, and partial response and prolonged disease control was obtained in November 2021, when progression took place. The patient's death occurred in March 2022.

Conclusions: This case report provides evidence on the efficacy of mTOR inhibitors as a treatment option in recurrent meningiomas. Furthermore, it highlights the importance of performing a molecular analysis as a preliminary step towards targeting the mTOR pathway.

Keywords: Bevacizumab; Everolimus; Malignant meningioma; mTOR mutation.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Female
  • Humans
  • MTOR Inhibitors
  • Meningeal Neoplasms* / drug therapy
  • Meningeal Neoplasms* / genetics
  • Meningeal Neoplasms* / pathology
  • Meningioma* / drug therapy
  • Meningioma* / genetics
  • Meningioma* / pathology
  • Neoplasm Recurrence, Local / drug therapy
  • Neoplasm Recurrence, Local / pathology
  • Precision Medicine
  • TOR Serine-Threonine Kinases / genetics
  • TOR Serine-Threonine Kinases / therapeutic use

Substances

  • MTOR Inhibitors
  • TOR Serine-Threonine Kinases
  • MTOR protein, human