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Abstract 1201: ALK amplification and rearrangements are recurrent targetable events in congenital and adult glioblastoma

Authors :
Anne-Florence Blandin
Ross Giglio
Maya Srikanth Graham
Guadalupe Garcia
Seth Malinowski
Jared K. Woods
Shakti Ramkissoon
Lori Ramkissoon
Frank Dubois
Kate Schoolcraft
Jessica W. Tsai
Dayle K. Wang
Robert Jones
Jayne Vogelzang
Kristine Pelton
Sarah Becker
Fiona Watkinson
Claire Sinai
Elizabeth Cohen
Matthew Booker
Michael Tolstorukov
Veerle Haemels
Liliana Goumnerova
Karen Wright
Mark Kieran
Katie Fehnel
David Reardon
Arnault Tauziede-Espariat
Rishi Lulla
Benjamin Carcamo
Stanley Chaleff
Alain Charest
Frederik De Smet
Azra H. Ligon
Adrian Dubuc
Melanie Pagès
Pascale Varlet
Patrick Wen
Brian Alexander
Susan Chi
Sanda Alexandrescu
Ralf Kittler
Robert Bachoo
Rameen Beroukhim
Pratiti Bandopadhayay
Keith L. Ligon
Source :
Cancer Research. 83:1201-1201
Publication Year :
2023
Publisher :
American Association for Cancer Research (AACR), 2023.

Abstract

Purpose: Anaplastic Lymphoma Kinase (ALK) aberrations have been identified in pediatric type infant gliomas, but their occurrence across age groups, functional effects, and treatment response have not been broadly established. Experimental Design: We performed a comprehensive analysis of ALK expression and genomic aberrations in both newly-generated and retrospective data from 371 glioblastomas (156 adult, 205 infant/pediatric and 10 congenital) with in vitro and in vivo validation of aberrations. Results: ALK aberrations at the protein or genomic level were detected in 12% of gliomas (45/371) in a wide age range (0-80 years). Recurrent as well as novel ALK fusions (LRRFIP1-ALK, DCTN1-ALK, PRKD3-ALK) were present in 50% (5/10) of congenital/infant, 1.4% (3/205) of pediatric, and 1.9% (3/156) of adult GBMs. ALK fusions were present as the only candidate driver in congenital/infant GBMs, and were sometimes focally amplified. In contrast, adult ALK fusions co-occurred with other oncogenic drivers. No activating ALK mutations were identified in any age group. Novel and recurrent ALK rearrangements promoted STAT3 and ERK1/2 pathways and transformation in vitro and in vivo. ALK-fused GBM cellular and mouse models were responsive to ALK inhibitors, including in patient cells derived from a congenital GBM. Relevant to treatment of infant gliomas, we showed that ALK protein appears minimally expressed in the forebrain at perinatal stages and no gross effects on perinatal brain development was seen in pregnant mice treated with the ALK inhibitor ceritinib. Conclusions: These findings support expanded evaluation of brain-penetrant ALK inhibitors in clinical trials across infant, pediatric, and adult GBMs. Citation Format: Anne-Florence Blandin, Ross Giglio, Maya Srikanth Graham, Guadalupe Garcia, Seth Malinowski, Jared K. Woods, Shakti Ramkissoon, Lori Ramkissoon, Frank Dubois, Kate Schoolcraft, Jessica W. Tsai, Dayle K. Wang, Robert Jones, Jayne Vogelzang, Kristine Pelton, Sarah Becker, Fiona Watkinson, Claire Sinai, Elizabeth Cohen, Matthew Booker, Michael Tolstorukov, Veerle Haemels, Liliana Goumnerova, Karen Wright, Mark Kieran, Katie Fehnel, David Reardon, Arnault Tauziede-Espariat, Rishi Lulla, Benjamin Carcamo, Stanley Chaleff, Alain Charest, Frederik De Smet, Azra H. Ligon, Adrian Dubuc, Melanie Pagès, Pascale Varlet, Patrick Wen, Brian Alexander, Susan Chi, Sanda Alexandrescu, Ralf Kittler, Robert Bachoo, Rameen Beroukhim, Pratiti Bandopadhayay, Keith L. Ligon. ALK amplification and rearrangements are recurrent targetable events in congenital and adult glioblastoma [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2023; Part 1 (Regular and Invited Abstracts); 2023 Apr 14-19; Orlando, FL. Philadelphia (PA): AACR; Cancer Res 2023;83(7_Suppl):Abstract nr 1201.

Subjects

Subjects :
Cancer Research
Oncology

Details

ISSN :
15387445
Volume :
83
Database :
OpenAIRE
Journal :
Cancer Research
Accession number :
edsair.doi...........7476108b30592be9f739f877e0770b64
Full Text :
https://doi.org/10.1158/1538-7445.am2023-1201