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Different time-dependent changes of risk for evolution in chronic lymphocytic leukemia with mutated or unmutated antigen B cell receptors

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F65269705%3A_____%2F19%3A00070996" target="_blank" >RIV/65269705:_____/19:00070996 - isvavai.cz</a>

  • Alternative codes found

    RIV/00216224:14740/19:00109738

  • Result on the web

    <a href="https://www.nature.com/articles/s41375-018-0322-7" target="_blank" >https://www.nature.com/articles/s41375-018-0322-7</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1038/s41375-018-0322-7" target="_blank" >10.1038/s41375-018-0322-7</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Different time-dependent changes of risk for evolution in chronic lymphocytic leukemia with mutated or unmutated antigen B cell receptors

  • Original language description

    Chronic lymphocytic leukemia (CLL) displays remarkable clinical heterogeneity, likely attributed to the underlying biological diversity [1]. This claim is supported by the fact that certain immunogenetic and/or genomic features identify subgroups of CLL patients with distinct prognosis and outcome [2,3,4]. Indeed, determination of the somatic hypermutation (SHM) status of the immunoglobulin heavy variable (IGHV) genes expressed by the clonotypic B cell receptor (BcR) and screening for aberrations οf the TP53 gene are nowadays considered essential for clinical decision making [5]. A cautionary note appears warranted when utilizing biomarkers, where the prognosis is usually assessed assuming stable predictability over the disease course; this hypothesis, however, is often unrealistic as it concerns genomic aberrations [6, 7]. Therefore, arguably, the prognostic power of a given biomarker may, instead, heavily depend on the time distance from diagnosis.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    30205 - Hematology

Result continuities

  • Project

    <a href="/en/project/LQ1601" target="_blank" >LQ1601: CEITEC 2020</a><br>

  • 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

    Leukemia

  • ISSN

    0887-6924

  • e-ISSN

  • Volume of the periodical

    33

  • Issue of the periodical within the volume

    7

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    5

  • Pages from-to

    1801-1805

  • UT code for WoS article

    000473724900022

  • EID of the result in the Scopus database

    2-s2.0-85060671726