HGG-37. CLINICAL AND MOLECULAR FEATURES OF BITHALAMIC GLIOMAS IN CHILDREN AND ADOLESCENTS: MULTICENTRIC STUDY AND META-ANALYSIS (2024)

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Marta Perez-Somarriba

The Royal Marsden NHS Foundation Trust

, London,

United Kingdom

Hospital Infantil Universitario Niño Jesús

, Madrid,

Spain

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,

Anoop Cherungonath

Birmingham Children´s Hospital

, Birmingham,

United Kingdom

The Royal Marsden NHS Foundation Trust

, London,

United Kingdom

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,

Ajla Wasti

University College London Hospital

, London,

United Kingdom

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Erika Pace

The Royal Marsden NHS Foundation Trust

, London,

United Kingdom

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Philip Benjamin

The Royal Marsden NHS Foundation Trust

, London,

United Kingdom

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Guillermo Villacampa

The Institute of Cancer Research

, London,

United Kingdom

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Zita Reisz

King’s College Hospital NHS Foundation Trust

, London,

United Kingdom

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Safa Al-Sarraj

King’s College Hospital NHS Foundation Trust

, London,

United Kingdom

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Leslie Bridges

St George’s Hospital NHS Foundation Trust

, London,

United Kingdom

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Thomas Jacques

Great Ormond Street Hospital for Children NHS Foundation Trust

, London,

United Kingdom

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Nagore Gene

Pediatric Cancer Center Barcelona

, Barcelona,

Spain

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Rita Pereira

The Institute of Cancer Research

, London,

United Kingdom

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Yura Grabovska

The Institute of Cancer Research

, London,

United Kingdom

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Alan Mackay

The Institute of Cancer Research

, London,

United Kingdom

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Ketty Kessler

The Institute of Cancer Research

, London,

United Kingdom

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Matthew Clarke

The Institute of Cancer Research

, London,

United Kingdom

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Vicente Santa-Maria

Pediatric Cancer Center Barcelona

, Barcelona,

Spain

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Ofelia Cruz

Pediatric Cancer Center Barcelona

, Barcelona,

Spain

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Andres Morales La Madrid

Pediatric Cancer Center Barcelona

, Barcelona,

Spain

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Anna Llort

Hospital Universitario Vall d´Hebrón

, Barcelona,

Spain

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Alvaro Lassaletta

Hospital Infantil Universitario Niño Jesús

, Madrid,

Spain

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Felisa Vazquez-Gomez

Hospital Infantil Universitario Niño Jesús

, Madrid,

Spain

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Elena Carceller

Hospital Universitario Gregorio Marañón

, Madrid,

Spain

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Carmen Garrido

Hospital Universitario Gregorio Marañón

, Madrid,

Spain

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Palma Solano-Paez

Hospital Universitario Virgen del Rocío

, Seville,

Spain

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Eduardo Quiroga

Hospital Universitario Virgen del Rocío

, Seville,

Spain

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Bassel Zebian

King’s College Hospital NHS Foundation Trust

, London,

United Kingdom

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Samantha Hettige

St George’s Hospital NHS Foundation Trust

, London,

United Kingdom

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Julia co*ckle

The Royal Marsden NHS Foundation Trust

, London,

United Kingdom

The Institute of Cancer Research

, London,

United Kingdom

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Henry Mandeville

The Royal Marsden NHS Foundation Trust

, London,

United Kingdom

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Paola Angelini

The Royal Marsden NHS Foundation Trust

, London,

United Kingdom

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Kavitha Srivatsa

University College London Hospital

, London,

United Kingdom

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Sucheta Vaidya

The Royal Marsden NHS Foundation Trust

, London,

United Kingdom

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Lynley Marshall

The Royal Marsden NHS Foundation Trust

, London,

United Kingdom

The Institute of Cancer Research

, London,

United Kingdom

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Chris Jones

The Institute of Cancer Research

, London,

United Kingdom

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Fernando Carceller

The Royal Marsden NHS Foundation Trust

, London,

United Kingdom

The Institute of Cancer Research

, London,

United Kingdom

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Neuro-Oncology, Volume 26, Issue Supplement_4, June 2024, Page 0, https://doi.org/10.1093/neuonc/noae064.321

Published:

18 June 2024

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    Marta Perez-Somarriba, Anoop Cherungonath, Ajla Wasti, Erika Pace, Philip Benjamin, Guillermo Villacampa, Zita Reisz, Safa Al-Sarraj, Leslie Bridges, Thomas Jacques, Cinzia Lavarino, Nagore Gene, Rita Pereira, Yura Grabovska, Alan Mackay, Ketty Kessler, Matthew Clarke, Vicente Santa-Maria, Ofelia Cruz, Andres Morales La Madrid, Anna Llort, Alvaro Lassaletta, Felisa Vazquez-Gomez, Elena Carceller, Carmen Garrido, Palma Solano-Paez, Eduardo Quiroga, Bassel Zebian, Samantha Hettige, Julia co*ckle, Henry Mandeville, Paola Angelini, Kavitha Srivatsa, Sucheta Vaidya, Lynley Marshall, Chris Jones, Fernando Carceller, HGG-37. CLINICAL AND MOLECULAR FEATURES OF BITHALAMIC GLIOMAS IN CHILDREN AND ADOLESCENTS: MULTICENTRIC STUDY AND META-ANALYSIS, Neuro-Oncology, Volume 26, Issue Supplement_4, June 2024, Page 0, https://doi.org/10.1093/neuonc/noae064.321

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Abstract

BACKGROUND

Bithalamic gliomas (BTG) are rare brain tumors with dismal prognosis. Optimal management and role of novel therapies have not been established yet. This study aimed to improve our understanding of BTG to guide adapted treatments.

METHODS

Retrospective case series across 6 Pediatric Neuro-Oncology Units (United Kingdom, Spain) of ≤18-year-old patients with BTG between 2000-2022. Clinical, pathological, and molecular data were derived and reviewed. A systematic review of the literature, meta-analysis, and survival analysis were performed.

RESULTS

Overall, 148 BTG cases were evaluated (study=25; literature=123). Of those, 97/148 (65%) had individual survival data. Median overall survival (mOS) (95%CI/range) was 13.2 months (12-16.8/0.6-262.2). mOS stratified by histological grading: 21.0 months (low-grade, n=32) versus 12.0 months (high-grade, n=55); hazard ratio (HR) 0.37 (95%CI 0.20-0.68), p-value=0.001. Molecular analyses (n=70) showed EGFR alterations (56%), TP53 mutations (30%), and H3K27M mutations (23%). mOS of EGFR-altered BTG based on targeted therapy was 13.2 months (no EGFR-inhibitors, n=26) versus 21.6 months (EGFR-inhibitors, n=9); HR 0.36 (95CI% 0.11-1.22). Methylation array data was generated for 4 patients and combined with 10 previously available profiles. Integrated MNP12.8 and mutation information classified 57% as DMG_EGFR and 21% as pedHGG_RTK2B. The remaining cases were classified as DMG_K27M (2/14) or pedHGG_A (1/14). Work is underway to establish a patient-derived EGFR-mutated BTG cell culture and further studies.

CONCLUSIONS

BTG have distinct radiological, and molecular features. EGFR alterations are seen in approximately half of BTG and H3K27M mutations are less frequent than in other midline high-grade gliomas (HGG). Low-grade histology is associated with a survival advantage, although still poor compared to pediatric low-grade gliomas. Therefore, treatment as per HGG guidelines should be considered for all BTG regardless of histological grading. EGFR-altered BTG patients can derive survival benefit from EGFR inhibitors, indicating that these should be considered as part of future treatment protocols.

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© The Author(s) 2024. Published by Oxford University Press on behalf of the Society for Neuro-Oncology.

This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact reprints@oup.com for reprints and translation rights for reprints. All other permissions can be obtained through our RightsLink service via the Permissions link on the article page on our site—for further information please contact journals.permissions@oup.com.

Issue Section:

Final category: High Grade Glioma

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