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Integrated genomic analysis reveals actionable targets in pediatric spinal cord low-grade gliomas
M. Adela, V. Ales, B. Petr, V. Katerina, S. David, S. Lucie, S. Lucie, K. Miroslav, Z. Josef, K. Martin, H. Zuzana, L. Petr, T. Jakub, B. Vladimir, P. Ivana, JTW. David, S. Martin, S. Terezia, K. Lenka, Z. Michal
Jazyk angličtina Země Anglie, Velká Británie
Typ dokumentu časopisecké články
Grantová podpora
NU21-07-00419
Ministry of Health of the Czech Republic
PRIMUS/19/MED/06
Charles University Grant Agency
00064203
MH CZ - DRO
GAUK 204220
Univerzita Karlova v Praze
LX22NPO5102
National Institute for Cancer Research (Programme EXCELES)
NLK
BioMedCentral
od 2013-12-01
BioMedCentral Open Access
od 2013
Directory of Open Access Journals
od 2013
Free Medical Journals
od 2013
PubMed Central
od 2013
Europe PubMed Central
od 2013
ProQuest Central
od 2015-01-01
Open Access Digital Library
od 2013-01-01
Open Access Digital Library
od 2013-01-01
Health & Medicine (ProQuest)
od 2015-01-01
ROAD: Directory of Open Access Scholarly Resources
od 2013
Springer Nature OA/Free Journals
od 2013-12-01
- MeSH
- astrocytom * genetika MeSH
- dítě MeSH
- genomika MeSH
- gliom * genetika patologie MeSH
- lidé MeSH
- mitogenem aktivované proteinkinasy kinas MeSH
- mladiství MeSH
- nádory míchy * genetika MeSH
- nádory mozku * genetika MeSH
- protoonkogenní proteiny B-raf genetika MeSH
- Check Tag
- dítě MeSH
- lidé MeSH
- mladiství MeSH
- Publikační typ
- časopisecké články MeSH
Gliomas are the most common central nervous tumors in children and adolescents. However, spinal cord low-grade gliomas (sLGGs) are rare, with scarce information on tumor genomics and epigenomics. To define the molecular landscape of sLGGs, we integrated clinical data, histology, and multi-level genetic and epigenetic analyses on a consecutive cohort of 26 pediatric patients. Driver molecular alteration was found in 92% of patients (24/26). A novel variant of KIAA1549:BRAF fusion (ex10:ex9) was identified using RNA-seq in four cases. Importantly, only one-third of oncogenic drivers could be revealed using standard diagnostic methods, and two-thirds of pediatric patients with sLGGs required extensive molecular examination. The majority (23/24) of detected alterations were potentially druggable targets. Four patients in our cohort received targeted therapy with MEK or NTRK inhibitors. Three of those exhibited clinical improvement (two with trametinib, one with larotrectinib), and two patients achieved partial response. Methylation profiling was implemented to further refine the diagnosis and revealed intertumoral heterogeneity in sLGGs. Although 55% of tumors clustered with pilocytic astrocytoma, other rare entities were identified in this patient population. In particular, diffuse leptomeningeal glioneuronal tumors (n = 3) and high-grade astrocytoma with piloid features (n = 1) and pleomorphic xanthoastrocytoma (n = 1) were present. A proportion of tumors (14%) had no match with the current version of the classifier. Complex molecular genetic sLGGs characterization was invaluable to refine diagnosis, which has proven to be essential in such a rare tumor entity. Moreover, identifying a high proportion of drugable targets in sLGGs opened an opportunity for new treatment modalities.
Division of Biostatistics German Cancer Research Center Heidelberg Germany
Hopp Children's Cancer Center Heidelberg Heidelberg Germany
Pediatric Glioma Research Group German Cancer Research Center Heidelberg Germany
Citace poskytuje Crossref.org
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