Immune checkpoint inhibitor therapy for recurrent meningiomas: a retrospective chart review

Priya Nidamanuri1, Jan Drappatz2

  • 1Department of Neurology, Division of Hematology-Oncology, University of Pittsburgh Medical Center, 5115 Centre Avenue, Pittsburgh, PA, 15232, USA. nidamanurip2@upmc.edu.

Abstract

Insights

Immunotherapy with anti-PD-1 inhibitors shows promise for recurrent meningiomas, particularly for high-grade tumors. This treatment offers a manageable safety profile and improved progression-free survival (PFS) and overall survival (OS) in select patients.

Area of Science:

  • Neuro-oncology
  • Immunotherapy
  • Meningioma Research

Background:

  • Meningiomas progressing after surgery and radiotherapy present a significant clinical challenge.
  • PD-1 and PD-L1 expression correlates with meningioma grade, indicating potential therapeutic targets.
  • Investigating immunotherapy is crucial for managing recurrent meningiomas.

Purpose of the Study:

  • To evaluate the efficacy and safety of anti-PD-1 inhibitor therapy in patients with recurrent meningiomas.
  • To describe progression-free survival (PFS) and overall survival (OS) in this patient cohort.
  • To identify potential predictive markers for treatment response.

Main Methods:

  • Retrospective chart review of patients treated with PD-1 inhibitors at UPMC Hillman Cancer Center.
  • Inclusion criteria: patients over 18 with meningioma receiving immunotherapy.
  • Treatment continued until disease progression, toxicity, death, or physician decision; radiographic assessments every 3-6 months.

Main Results:

  • Eight patients received anti-PD-1 therapy between January 2015 and November 2021.
  • Median PFS was 7 months and median OS was 1.75 years.
  • Patients with positive PD-1/PD-L1 expression showed improved outcomes: median PFS of 2 years and median OS of 3 years.

Conclusions:

  • Anti-PD-1 therapy demonstrates a manageable safety profile in recurrent meningioma patients.
  • WHO Grade III tumors and positive PD-1/PD-L1 expression are associated with enhanced PFS and OS.
  • Further research with larger cohorts is warranted to confirm immunotherapy's role in meningioma treatment.

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