Alterations in ALK/ROS1/NTRK/MET drive a group of infantile hemispheric gliomas
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00064203%3A_____%2F19%3A10398552" target="_blank" >RIV/00064203:_____/19:10398552 - isvavai.cz</a>
Alternative codes found
RIV/00216208:11130/19:10398552
Result on the web
<a href="https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=Aeo24fUxCG" target="_blank" >https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=Aeo24fUxCG</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1038/s41467-019-12187-5" target="_blank" >10.1038/s41467-019-12187-5</a>
Alternative languages
Result language
angličtina
Original language name
Alterations in ALK/ROS1/NTRK/MET drive a group of infantile hemispheric gliomas
Original language description
Infant gliomas have paradoxical clinical behavior compared to those in children and adults: low-grade tumors have a higher mortality rate, while high-grade tumors have a better outcome. However, we have little understanding of their biology and therefore cannot explain this behavior nor what constitutes optimal clinical management. Here we report a comprehensive genetic analysis of an international cohort of clinically annotated infant gliomas, revealing 3 clinical subgroups. Group 1 tumors arise in the cerebral hemispheres and harbor alterations in the receptor tyrosine kinases ALK, ROS1, NTRK and MET. These are typically single-events and confer an intermediate outcome. Groups 2 and 3 gliomas harbor RAS/MAPK pathway mutations and arise in the hemispheres and midline, respectively. Group 2 tumors have excellent long-term survival, while group 3 tumors progress rapidly and do not respond well to chemoradiation. We conclude that infant gliomas comprise 3 subgroups, justifying the need for specialized therapeutic strategies.
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
2019
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Nature Communications [online]
ISSN
2041-1723
e-ISSN
—
Volume of the periodical
10
Issue of the periodical within the volume
September
Country of publishing house
GB - UNITED KINGDOM
Number of pages
13
Pages from-to
4343
UT code for WoS article
000487585600004
EID of the result in the Scopus database
2-s2.0-85072668903