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Venetoclax plus bortezomib and dexamethasone in heavily pretreated end-stage myeloma patients without t(11;14): A real-world cohort

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61988987%3A17110%2F20%3AA21025RF" target="_blank" >RIV/61988987:17110/20:A21025RF - isvavai.cz</a>

  • Alternative codes found

    RIV/00843989:_____/20:E0108506

  • Result on the web

    <a href="https://onlinelibrary.wiley.com/doi/epdf/10.1002/hon.2736" target="_blank" >https://onlinelibrary.wiley.com/doi/epdf/10.1002/hon.2736</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1002/hon.2736" target="_blank" >10.1002/hon.2736</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Venetoclax plus bortezomib and dexamethasone in heavily pretreated end-stage myeloma patients without t(11;14): A real-world cohort

  • Original language description

    Multiple myeloma (MM) is the second most common blood cancer caused by the uncontrolled proliferation of clonal plasma cells. Despite recent advances in treatment, a majority of patients eventually relapse and die because of progressive disease (PD). Thus, the development of modern molecules with novel mechanisms of action is needed. The overexpression of antiapoptotic proteins (ie, Bcl‐2, Bcl‐XL, Mcl‐1) represents one of the hallmarks of cancer that favors tumor cell survival. It has been demonstrated that a subset of MM is Bcl‐2 dependent. These are especially those harboring the t(11;14)—molecular subgroup which is associated with a high expression of Bcl‐2 and a low expression of Bcl‐XL and Mcl‐1.1, 2 The presence of translocation t(11;14) is present in 15%‐20% of newly diagnosed MM3 and even up in 50% of primary plasma cell leukemia.4

  • 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

  • Continuities

    S - Specificky vyzkum na vysokych skolach

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

    HEMATOLOGICAL ONCOLOGY

  • ISSN

    0278-0232

  • e-ISSN

    1099-1069

  • Volume of the periodical

    38

  • Issue of the periodical within the volume

    3

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    3

  • Pages from-to

    412-414

  • UT code for WoS article

    000527833100001

  • EID of the result in the Scopus database