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Salvage therapies for first relapse of SHH medulloblastoma in early childhood

  • Craig Erker
  • , Martin Mynarek
  • , Marie Simbozel
  • , Brandon T. Craig
  • , Virginia L. Harrod
  • , Andrea M. Cappellano
  • , Kenneth J. Cohen
  • , Vicente Santa Maria Lopez
  • , Andres Morales La Madrid
  • , Chantel Cacciotti
  • , Lorena Baroni
  • , Ralph Salloum
  • , Ashley S. Margol
  • , George Michaiel
  • , Dolly Aguilera
  • , Claire M. Mazewski
  • , Cassie N. Kline
  • , Jonathan L. Finlay
  • , Mohamed S. Abdelbaki
  • , Jeffrey C. Murray
  • Kathleen Dorris, Bruce Crooks, Kevin F. Ginn, Nisreen Amayiri, Stephan Tippelt, Gudrun Fleischhack, Svenja Tonn, Nicolas U. Gerber, Alvaro Lassaletta, Jordan R. Hansford, Sara Khan, Stephen W. Gilheeney, Lindsey M. Hoffman, Michal Zapotocky, Valérie Larouche, Shafqat Shah, Vijay Ramaswamy, Amar Gajjar, Sébastien Perreault, Sabine Mueller, Juliette Hukin, Sylvia Cheng, Zhihong J. Wang, Kara Matheson, Simon Bailey, Eric Bouffet, Steven C. Clifford, Giles Robinson, Christelle Dufour, Stefan Rutkowski, Lucie Lafay-Cousin

Research output: Contribution to journal › Article › peer-review

Abstract

Background Sonic hedgehog (SHH) medulloblastoma is the most common molecular group of infant and early childhood medulloblastoma (iMB) and has no standard of care at relapse. This work aimed to evaluate the post-relapse survival (PRS) and explore prognostic factors of patients with nodular desmoplastic (ND) and/or SHH iMB. Methods This international retrospective study included 147 subjects diagnosed with relapsed ND/SHH iMB between 1995 and 2017, <6 years old at original diagnosis, and treated without initial craniospinal irradiation (CSI). Univariable and multivariable Cox models with propensity score analyses were used to assess PRS for those in the curative intent cohort. Results The 3-year PRS was 61.6% (95% confidence interval [CI], 52.2-69.6). The median age at relapse was 3.4 years (interquartile range [IQR], 2.6-4.1). Those with local relapse (40.8%) more often received salvage treatment with surgery (P<.001), low-dose CSI (≤24 Gy; P<.001), or focal radiotherapy (P=.008). Patients not receiving CSI (40.5%) more often received salvage marrow-ablative chemotherapy (HDC + AuHCR [P<.001]). On multivariable analysis, CSI was associated with improved survival (hazard ratio [HR] 0.33 [95% CI, 0.13-0.86], P=.04). Salvage HDC + AuHCR, while clinically important, did not reach statistical significance (HR 0.24 [95% CI, 0.0054-1.025], P=.065). Conclusions Survival of patients with relapsed SHH iMB is not satisfactory and relies on treatments associated with toxicities including CSI and/or HDC + AuHCR. Cure at initial diagnosis to avoid relapse is crucial. For patients with localized relapse undergoing resection, alternative salvage regimens that avoid high-dose CSI (>24 Gy) can be considered.

Original languageEnglish
Pages (from-to)2158-2169
Number of pages12
JournalNeuro-Oncology
Volume27
Issue number8
DOIs
Publication statusPublished or Issued - 1 Aug 2025
Externally publishedYes

Keywords

  • SHH
  • infant and early childhood
  • medulloblastoma
  • relapse

ASJC Scopus subject areas

  • Oncology
  • Clinical Neurology
  • Cancer Research

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