Radiation-induced gliomas represent H3-/IDH-wild type pediatric gliomas with recurrent PDGFRA amplification and loss of CDKN2A/B

Author:

Deng Maximilian Y.ORCID,Sturm DominikORCID,Pfaff Elke,Sill Martin,Stichel Damian,Balasubramanian Gnana Prakash,Tippelt Stephan,Kramm Christof,Donson Andrew M.,Green Adam L.ORCID,Jones Chris,Schittenhelm JensORCID,Ebinger MartinORCID,Schuhmann Martin U.,Jones Barbara C.,van Tilburg Cornelis M.,Wittmann Andrea,Golanov Andrey,Ryzhova Marina,Ecker Jonas,Milde TillORCID,Witt Olaf,Sahm FelixORCID,Reuss David,Sumerauer David,Zamecnik Josef,Korshunov Andrey,von Deimling AndreasORCID,Pfister Stefan M.,Jones David T. W.ORCID

Abstract

AbstractLong-term complications such as radiation-induced second malignancies occur in a subset of patients following radiation-therapy, particularly relevant in pediatric patients due to the long follow-up period in case of survival. Radiation-induced gliomas (RIGs) have been reported in patients after treatment with cranial irradiation for various primary malignancies such as acute lymphoblastic leukemia (ALL) and medulloblastoma (MB). We perform comprehensive (epi-) genetic and expression profiling of RIGs arising after cranial irradiation for MB (n = 23) and ALL (n = 9). Our study reveals a unifying molecular signature for the majority of RIGs, with recurrent PDGFRA amplification and loss of CDKN2A/B and an absence of somatic hotspot mutations in genes encoding histone 3 variants or IDH1/2, uncovering diagnostic markers and potentially actionable targets.

Publisher

Springer Science and Business Media LLC

Subject

General Physics and Astronomy,General Biochemistry, Genetics and Molecular Biology,General Chemistry

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