Publication

High-risk Meningioma: Initial Outcomes From NRG Oncology/RTOG 0539

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Last modified
  • 08/19/2025
Type of Material
Authors
    Leland C Rogers, St. Joseph’s Hospital and Medical CenterMinhee Won, American College of RadiologyMichael A Vogelbaum, Moffitt Cancer Center, Tampa, FloridaHui-Kuo Shu, Emory UniversityArie Perry, University of California San FranciscoLynn S Ashby, St. Joseph’s Hospital and Medical CenterJignesh M Modi, Yale New Haven HospitalAnthony M Alleman, University of OklahomaJames Galvin, Imaging & Radiat Oncol Core PhiladelphiaShannon E Fogh, University of California San FranciscoEmad Youssef, St. Joseph’s Hospital and Medical CenterNimisha Deb, St. Luke’s University Health NetworkYoung Kwok, University of MarylandClifford G Robinson, Washington UniversityBarbara J Fisher, London Regional Cancer ProgramValerie Panet-Raymond, McGill UniversityWilliam G McMillan, McMaster UniversityJohn F de Groot, Univ Texas MD Anderson Canc CtrPeixin Zhang, American College of RadiologyMinesh P Mehta, Baptist Health, Miami
Language
  • English
Date
  • 2020-03-15
Publisher
  • ELSEVIER SCIENCE INC
Publication Version
Copyright Statement
  • © 2019 Elsevier Inc. All rights reserved.
License
Final Published Version (URL)
Title of Journal or Parent Work
Volume
  • 106
Issue
  • 4
Start Page
  • 790
End Page
  • 799
Grant/Funding Information
  • This study was supported by National Cancer Institute grants U10CA180868 and U10CA180822
Abstract
  • Background: Phase 2 cooperative group meningioma trial assessing the safety and efficacy of risk-adaptive management strategies. This is the initial analysis of the high-risk cohort. Methods and Materials: High-risk patients were those with a new or recurrent World Health Organization (WHO) grade III meningioma of any resection extent, recurrent WHO grade II of any resection extent, or new WHO grade II after subtotal resection. Patients received intensity-modulated radiotherapy (IMRT) using a simultaneous integrated boost technique (60 Gy high dose and 54 Gy low dose in 30 fractions). Three-year progression-free survival (PFS) was the primary endpoint. Adverse events (AEs) were scored per NCI Common Terminology Criteria for Adverse Events version 3. Results: Of 57 enrolled patients, 53 received protocol treatment. Median follow-up was 4.0 years (4.8 years for living patients). Two patients withdrew without progression before year 3; for the remaining 51 patients, 3-year PFS was 58.8%. Among all 53 protocol-treated patients, 3-year PFS was 59.2%. Three-year local control was 68.9%, and overall survival was 78.6%. Of 51 patients, 1 patient (1.9%) experienced a late grade-5 necrosis-related AE. All other acute (23 of 53 patients) and late (21 of 51 patients) AEs were grades 1 to 3. Conclusions: Patients with high-risk meningioma treated with IMRT (60 Gy/30) experienced 3-year PFS of 58.8%. Combined acute and late AEs were limited to grades 1 to 3, except for a single necrosis-related grade 5 event. These results support postoperative IMRT for high-risk meningioma and invite ongoing investigations to improve outcomes further.
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