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MRI and Molecular Characterization of Pediatric High-Grade Midline Thalamic Gliomas: The HERBY Phase II Trial

Rodriguez, Daniel; Calmon, Raphael; Aliaga, Esther Sanchez; Warren, Daniel; Warmuth-Metz, Monika; Jones, Chris; Mackay, Alan; Varlet, Pascale; Le Deley, Marie Cécile; Hargrave, Darren; Cañete, Adela; Massimino, Maura; Azizi, Amedeo A.; Saran, Frank; Zahlmann, Gudrun; Garcia, Josep; Vassal, Gilles; Grill, Jacques; Peet, Andrew; Dineen, Robert A.; Morgan, Paul S.; Jaspan, Timothy

MRI and Molecular Characterization of Pediatric High-Grade Midline Thalamic Gliomas: The HERBY Phase II Trial Thumbnail


Authors

Daniel Rodriguez

Raphael Calmon

Esther Sanchez Aliaga

Daniel Warren

Monika Warmuth-Metz

Chris Jones

Alan Mackay

Pascale Varlet

Marie Cécile Le Deley

Darren Hargrave

Adela Cañete

Maura Massimino

Amedeo A. Azizi

Frank Saran

Gudrun Zahlmann

Josep Garcia

Gilles Vassal

Jacques Grill

Andrew Peet

Paul S. Morgan

Timothy Jaspan



Abstract

Background Diffuse midline gliomas (DMG) are characterized by a high incidence of H3 K27 mutations and poorer outcome. The HERBY trial has provided one of the largest cohorts of pediatric DMGs with available radiologic, histologic-genotypic, and survival data. Purpose To define MRI and molecular characteristics of DMG. Materials and Methods This study is a secondary analysis of a prospective trial (HERBY; ClinicalTrials.gov identifier, NCT01390948) undertaken between October 2011 and February 2016. Among 121 HERBY participants, 50 had midline nonpontine-based tumors. Midline high-grade gliomas were reclassified into DMG H3 K27 mutant, H3 wild type with enhancer of zest homologs inhibitory protein overexpression, epidermal growth factor receptormutant, or not otherwise stated. The epicenter of each tumor and other radiologic characteristics were ascertained from MRI and correlated with the new subtype classification, histopathologic characteristics, surgical extent, and outcome parameters. Kaplan-Meier curves and log-rank tests were applied to determine and describe survival differences between groups. Results There were 42 participants (mean age, 12 years ± 4 [SD]; 23 girls) with radiologically evaluable thalamic-based DMG. Eighteen had partial thalamic involvement (12 thalamopulvinar, six anteromedial), 10 involved a whole thalamus, nine had unithalamic tumors with diffuse contiguous extension, and five had bithalamic tumors (two symmetric, three partial). Twenty-eight participants had DMG H3 K27 mutant tumors; there were no differences in outcome compared with other DMGs (n = 4). Participants who underwent major debulking or total or near-total resection had longer overall survival (OS): 18.5 months vs 11.4 months (P = .02). Enrolled participants who developed leptomeningeal metastatic dissemination before starting treatment had worse outcomes (event-free survival, 2.9 months vs 8.0 months [P = .02]; OS, 11.4 months vs 18.5 months [P = .004]). Conclusion Thalamic involvement of diffuse midline gliomas ranged from localized partial thalamic to holo- or bithalamic with diffuse contiguous spread and had poor outcomes, irrespective of H3 K27 subtype alterations. Leptomeningeal dissemination and less than 50% surgical resection were adverse risk factors for survival. Clinical trial registration no. NCT01390948 © RSNA, 2022 Online supplemental material is available for this article. See also the editorial by Widjaja in this issue.

Citation

Rodriguez, D., Calmon, R., Aliaga, E. S., Warren, D., Warmuth-Metz, M., Jones, C., Mackay, A., Varlet, P., Le Deley, M. C., Hargrave, D., Cañete, A., Massimino, M., Azizi, A. A., Saran, F., Zahlmann, G., Garcia, J., Vassal, G., Grill, J., Peet, A., Dineen, R. A., …Jaspan, T. (2022). MRI and Molecular Characterization of Pediatric High-Grade Midline Thalamic Gliomas: The HERBY Phase II Trial. Radiology, 304(1), 174-182. https://doi.org/10.1148/radiol.211464

Journal Article Type Article
Acceptance Date Nov 3, 2021
Online Publication Date Apr 12, 2022
Publication Date Jul 1, 2022
Deposit Date Dec 17, 2021
Publicly Available Date Oct 13, 2022
Journal Radiology
Print ISSN 0033-8419
Electronic ISSN 1527-1315
Publisher Radiological Society of North America
Peer Reviewed Peer Reviewed
Volume 304
Issue 1
Pages 174-182
DOI https://doi.org/10.1148/radiol.211464
Keywords Radiology, Nuclear Medicine and imaging
Public URL https://nottingham-repository.worktribe.com/output/7022086
Publisher URL https://pubs.rsna.org/doi/10.1148/radiol.211464

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