CTP-11. Biological Medicines for Diffuse Intrinsic Pontine Gliomas (DIPG) Eradication (BIOMEDE). An International Randomized Phase II Biomarker-driven Platform Trial Comparing Three Targeted Therapies in Combination with Radiotherapy

Abstract DIPG is the most aggressive brain cancer. Radiotherapy offers transient palliation but survival could not be improved significantly since 50 years. 233 patients with biopsy-confirmed DIPG harboring H3K27me3 loss were randomized to one of the three drugs (erlotinib, everolimus or dasatinib) in addition to radiotherapy. Immunohistochemical biomarkers were assessed centrally together with whole exome and RNA sequencing. Treatment allocation was designed so that a drug could not be randomized if the corresponding biomarker was absent in the tumor. Toxicity was manageable, everolimus showing significantly less adverse events. With a median follow-up of 5.3 years, median OS from the date of treatment start was 9.0, 11.3 and 9.4 months for erlotinib, everolimus and dasatinib, respectively (p=NS). The presence of TP53 mutations frequently associated with numerous structural chromosomal aberrations was the strongest predictor for poor survival (HR of 2.552; 95% CI = 1.476-3.345; p=0.0002). Mutations in the mTOR pathway or its pathway activation on gene expression analysis were associated with a better response to everolimus. Four long-term survivors all treated with everolimus were alive more than six years from diagnosis.

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Publication Details

Journal
Neuro-Oncology
Published
2025-11-01
DOI
https://doi.org/10.1093/neuonc/noaf201.0583
Primary Topic
Glioma Diagnosis and Treatment
Type
article
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article

CTP-11. Biological Medicines for Diffuse Intrinsic Pontine Gliomas (DIPG) Eradication (BIOMEDE). An International Randomized Phase II Biomarker-driven Platform Trial Comparing Three Targeted Therapies in Combination with Radiotherapy

Gwénaël Le Teuff, Geoffrey McCowage, Patricia Blanc, Darren Hargrave et al.
Neuro-Oncology
Glioma Diagnosis and Treatment
article

CTP-11. Biological Medicines for Diffuse Intrinsic Pontine Gliomas (DIPG) Eradication (BIOMEDE). An International Randomized Phase II Biomarker-driven Platform Trial Comparing Three Targeted Therapies in Combination with Radiotherapy

Gwénaël Le Teuff, Geoffrey McCowage, Patricia Blanc, Darren Hargrave, Marie‐Anne Debily, Klas Blomgren, Stéphanie Bolle, Chris Jones, Dannis G. van Vuurden, Laurent Riffaud, Kévin Beccaria, Raphaël Calmon, David S. Ziegler, Nathalie Boddaert, Anne‐Isabelle Bertozzi, Francisco Bautista, Émilie De Carli, Gilles Vassal, Thomas Kergrohen, David Castel, Kristian Aquilina, Pascale Varlet, Samuel Abbou, Karsten Nysom, E. Barret, Angokai Moussa, Pierre Leblond, Jacques Grill, Stéphanie Puget, Deley Le Marie-Cécile
article en

Abstract

Abstract DIPG is the most aggressive brain cancer. Radiotherapy offers transient palliation but survival could not be improved significantly since 50 years. 233 patients with biopsy-confirmed DIPG harboring H3K27me3 loss were randomized to one of the three drugs (erlotinib, everolimus or dasatinib) in addition to radiotherapy. Immunohistochemical biomarkers were assessed centrally together with whole exome and RNA sequencing. Treatment allocation was designed so that a drug could not be randomized if the corresponding biomarker was absent in the tumor. Toxicity was manageable, everolimus showing significantly less adverse events. With a median follow-up of 5.3 years, median OS from the date of treatment start was 9.0, 11.3 and 9.4 months for erlotinib, everolimus and dasatinib, respectively (p=NS). The presence of TP53 mutations frequently associated with numerous structural chromosomal aberrations was the strongest predictor for poor survival (HR of 2.552; 95% CI = 1.476-3.345; p=0.0002). Mutations in the mTOR pathway or its pathway activation on gene expression analysis were associated with a better response to everolimus. Four long-term survivors all treated with everolimus were alive more than six years from diagnosis.

Neuro-OncologyVol. 27(Supplement_5)
Hôpital Necker-Enfants Malades (FR), Great Ormond Street Hospital (GB), Institut Gustave Roussy (FR), Children's Hospital at Westmead (AU), Copenhagen University Hospital (DK), Rigshospitalet (DK), Karolinska Institutet (SE), Université Rennes 2 (FR), Centre Léon Bérard (FR), Centre Hospitalier Universitaire d'Angers (FR), Centre Hospitalier Sainte-Anne (FR), Sydney Children's Hospital (AU), Princess Máxima Center (NL), Centre Oscar Lambret (FR), Hôpital des Enfants (FR), Centre Hospitalier Universitaire de Rennes (FR), Institut des Maladies Génétiques Imagine (FR), University College London (GB), Université d'Angers (FR), Université de Rennes (FR), Université d'Évry Val-d'Essonne (FR)
Openalex Percentile: Top 51%
Glioma Diagnosis and Treatment
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