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February 28, 2026Journal of Neuro-Oncology0 citationsOpen Access

Clinical and translational progress in oncolytic virotherapy for pediatric CNS tumors

AEAmr ElgehinyAFAaron E. FanMFMaria Frost

Key Points

  • The aim is to evaluate the current status and future directions of oncolytic virotherapy for pediatric CNS tumors.
  • Summarized findings from pediatric clinical trials of oncolytic viruses.
  • Highlighted HSV-based agents, adenoviral vectors, and other viral platforms.
  • Reviewed limitations of early-phase data and imaging challenges.
  • Discussed preclinical studies and early-phase trials for safety and efficacy.
  • Demonstrated encouraging safety and efficacy signals from early-phase clinical trials.
  • Identified challenges like pseudoprogression that affect treatment outcomes.
  • Highlighted promising innovations in viral engineering and delivery methods.

Abstract

Pediatric central nervous system (CNS) tumors are the leading cause of cancer-related mortality in children. Development of more effective therapies for pediatric CNS tumors has been slow, underscoring an urgent need for novel and innovative approaches. This review summarizes current pediatric clinical trials of oncolytic viruses for pediatric brain tumors including high-grade glioma (HGG), diffuse midline glioma (DMG), medulloblastoma (MDB), atypical teratoid rhabdoid tumors (ATRT), and other high-grade tumors, while highlighting limitations of early-phase data, exploratory biomarkers, imaging challenges, pseudoprogression, and future directions. Key platforms include HSV-based agents (HSV1716, G207, and M032); adenoviral vectors (DNX2401, Ad-TD-nsIL12, and ICOVIR-5); MV-NIS (measles virus); PVS-RIPO (poliovirus); and Reolysin (reovirus). We review trial status, innovations in viral engineering and delivery, combinatorial strategies and translational challenges to establish oncolytic virotherapy as part of the future standard care for pediatric brain tumors. Oncolytic virotherapy or immunovirotherapy offers a promising strategy to selectively kill tumor cells and generate antitumor immune response while minimizing toxicity to healthy cells compared to conventional treatments. Although still emerging in pediatric neuro-oncology, preclinical studies and early-phase clinical trials show encouraging safety and efficacy signals. Not applicable.

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Cite This Study

Elgehiny et al. (2026) studied this question.

synapsesocial.com/papers/69a285da0a974eb0d3c00c6ehttps://doi.org/10.1007/s11060-026-05480-z
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