Prediction of response to anti-EGFR antibody-based therapies by multigene sequencing in colorectal cancer patients.
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216224%3A14740%2F15%3A00084505" target="_blank" >RIV/00216224:14740/15:00084505 - isvavai.cz</a>
Alternative codes found
RIV/00209805:_____/15:#0000695
Result on the web
<a href="http://bmccancer.biomedcentral.com/articles/10.1186/s12885-015-1752-5" target="_blank" >http://bmccancer.biomedcentral.com/articles/10.1186/s12885-015-1752-5</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1186/s12885-015-1752-5" target="_blank" >10.1186/s12885-015-1752-5</a>
Alternative languages
Result language
angličtina
Original language name
Prediction of response to anti-EGFR antibody-based therapies by multigene sequencing in colorectal cancer patients.
Original language description
Background: The anti-epidermal growth factor receptor (EGFR) monoclonal antibodies (moAbs) cetuximab or panitumumab are administered to colorectal cancer (CRC) patients who harbor wild-type RAS proto-oncogenes. However, a percentage of patients do not respond to this treatment. In addition to mutations in the RAS genes,mutations in other genes, such as BRAF, PI3KCA,or PTEN, could be involved in the resistance to anti-EGFR moAb therapy. Methods: In order to develop a comprehensive approach for the detection of mutations and to eventually identify other genes responsible for resistance to anti-EGFR moAbs, we investigated a panel of 21 genes by parallel sequencing on the Ion Torrent Personal Genome Machine platform. We sequenced 65 CRCs that were treatedwith cetuximab or panitumumab. Among these, 37 samples were responsive and 28 were resistant.
Czech name
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Czech description
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Classification
Type
J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)
CEP classification
FD - Oncology and haematology
OECD FORD branch
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Result continuities
Project
Result was created during the realization of more than one project. More information in the Projects tab.
Continuities
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)
Others
Publication year
2015
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
BMC Cancer
ISSN
1471-2407
e-ISSN
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Volume of the periodical
15
Issue of the periodical within the volume
October
Country of publishing house
GB - UNITED KINGDOM
Number of pages
11
Pages from-to
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UT code for WoS article
000363502400001
EID of the result in the Scopus database
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