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Feasibility and Safety of High-Dose Proton Re-Irradiation in Recurrent Pediatric Central Nervous System Tumors: A Single-Institution Retrospective Study

  • Jin Ho Song
  • , Jonathan Baron
  • , Carlos Chavez Perez
  • , Sidharth Ramesh
  • , Jane Minturn
  • , Kavita A. Desai
  • , Amish C. Shah
  • , Jean M. Belasco
  • , Kristina A. Cole
  • , Michael J. Fisher
  • , Phillip B. Storm
  • , Peter M. Madsen
  • , Goldie Kurtz
  • , Robert A. Lustig
  • , Christine Hill-Kayser
  • , Michael J. LaRiviere
  • University of Pennsylvania
  • The Children's Hospital of Philadelphia

Research output: Contribution to journalArticlepeer-review

Abstract

Purpose: Pediatric central nervous system (CNS) tumors often recur despite multimodality therapy. Although re-irradiation (re-RT) has historically been limited by concerns for severe late toxicities, modern techniques have renewed interest in this approach. Proton therapy provides dosimetric advantages that may enable curative re-treatment with reduced normal tissue exposure. Methods: We retrospectively reviewed 54 pediatric patients who underwent proton re-RT for recurrent CNS tumors at our institution (2010–2024). Eligible patients had received prior CNS-directed RT at ≤20 years of age. Toxicities were graded per Common Terminology Criteria for Adverse Events (CTCAE) v5.0 as acute (<3 months) or late (≥3 months). Cumulative dosimetry was assessed by registering RT1 and RT2 plans and converting doses to EQD2 (α/β = 2 Gy). Overall survival (OS) and progression-free survival (PFS) were estimated using Kaplan–Meier methods. Results: Median age at re-RT was 11 years, with a median interval of 28.5 months between RT courses. The median prescribed re-RT dose was 54 Gy (range, 25–60), yielding a cumulative EQD2 of 102.6 Gy (range, 46.8–112.9). Median OS and PFS were 46.0 and 16.5 months, respectively. Among 16 ependymoma patients, all received full-dose proton re-RT (54–59.4 Gy), yielding a 1-year OS of 91.7% and PFS of 50.0%. Glioma patients had inferior outcomes (1-year OS 55.4%, PFS 41.6%) with a median re-RT EQD2 of 48.1 Gy. An RT interval of ≥12 months was associated with improved OS and PFS. Composite dosimetry in 21 patients showed a median cumulative brain D0.1cc of 109.0 Gy; only one patient developed Grade 3 radiation necrosis (RN). High-grade acute toxicity occurred in 13.0% of patients, all manageable with supportive care. Conclusion: Proton re-RT for pediatric CNS tumors is feasible and associated with encouraging survival and low rates of serious late toxicity.

Original languageEnglish
Article numbere70371
JournalPediatric Blood and Cancer
Volume73
Issue number7
DOIs
StatePublished - Jul 2026

Bibliographical note

Publisher Copyright:
© 2026 The Author(s). Pediatric Blood & Cancer published by Wiley Periodicals LLC.

Keywords

  • neuro-oncology
  • pediatric CNS tumors
  • proton therapy
  • radiation oncology
  • re-irradiation

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