Integrated Molecular and Clinical Analysis of 1,000 Pediatric Low-Grade Gliomas
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11130%2F20%3A10410749" target="_blank" >RIV/00216208:11130/20:10410749 - isvavai.cz</a>
Alternative codes found
RIV/00064203:_____/20:10410749
Result on the web
<a href="https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=msLGXoc0dm" target="_blank" >https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=msLGXoc0dm</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1016/j.ccell.2020.03.011" target="_blank" >10.1016/j.ccell.2020.03.011</a>
Alternative languages
Result language
angličtina
Original language name
Integrated Molecular and Clinical Analysis of 1,000 Pediatric Low-Grade Gliomas
Original language description
Pediatric low-grade gliomas (pLGG) are frequently driven by genetic alterations in the RAS-mitogen-activated protein kinase (RAS/MAPK) pathway yet show unexplained variability in their clinical outcome. To address this, we characterized a cohort of >1,000 clinically annotated pLGG. Eighty-four percent of cases harbored a driver alteration, while those without an identified alteration also often exhibited upregulation of the RAS/MAPK pathway. pLGG could be broadly classified based on their alteration type. Rearrangement-driven tumors were diagnosed at a younger age, enriched for WHO grade I histology, infrequently progressed, and rarely resulted in death as compared with SNV-driven tumors. Further sub-classification of clinical-molecular correlates stratified pLGG into risk categories. These data highlight the biological and clinical differences between pLGG subtypes and opens avenues for future treatment refinement.
Czech name
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Czech description
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Classification
Type
J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database
CEP classification
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OECD FORD branch
30204 - Oncology
Result continuities
Project
—
Continuities
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Others
Publication year
2020
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Cancer Cell
ISSN
1535-6108
e-ISSN
—
Volume of the periodical
37
Issue of the periodical within the volume
4
Country of publishing house
US - UNITED STATES
Number of pages
15
Pages from-to
569-583
UT code for WoS article
000526112000015
EID of the result in the Scopus database
2-s2.0-85082748299