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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

  • Czech description

Classification

  • Type

    J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

  • CEP classification

    FD - Oncology and haematology

  • OECD FORD branch

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

  • 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

  • UT code for WoS article

    000363502400001

  • EID of the result in the Scopus database