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Targeting CD38 with isatuximab and a novel CD38/CD3xCD28 trispecific T-cell engager in older patients with acute myeloid leukemia

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00843989%3A_____%2F24%3AE0111070" target="_blank" >RIV/00843989:_____/24:E0111070 - isvavai.cz</a>

  • Result on the web

    <a href="https://ashpublications.org/bloodadvances/article/8/15/3875/516313/Targeting-CD38-with-isatuximab-and-a-novel-CD38" target="_blank" >https://ashpublications.org/bloodadvances/article/8/15/3875/516313/Targeting-CD38-with-isatuximab-and-a-novel-CD38</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1182/bloodadvances.2024013212" target="_blank" >10.1182/bloodadvances.2024013212</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Targeting CD38 with isatuximab and a novel CD38/CD3xCD28 trispecific T-cell engager in older patients with acute myeloid leukemia

  • Original language description

    Acute myeloid leukemia (AML) is the most common acute leukemia in adults and its prevalence significantly increases in older patients. Furthermore, while the 5-year rate of overall survival (OS) for adults younger than 60 is around 40%, it decreases to 10% in patients above this age. The treatment landscape of AML is evolving from a curative/intensive vs palliative/low-intensity binary approach into new strategies that incorporate mutation-specific targeted therapies, apoptosis-inducing small molecules, and immunotherapy. Nonetheless, older patients who are unable to receive intensive chemotherapy with acceptable side effects and patients with relapsed/refractory disease continue to have dismal survival rates. Thus, the identification of new targets and treatment modalities is an unmet need.

  • 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

    V - Vyzkumna aktivita podporovana z jinych verejnych zdroju

Others

  • Publication year

    2024

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Blood advances

  • ISSN

    2473-9537

  • e-ISSN

    2473-9537

  • Volume of the periodical

    8

  • Issue of the periodical within the volume

    15

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    5

  • Pages from-to

    3875-3879

  • UT code for WoS article

    001284281200001

  • EID of the result in the Scopus database

    2-s2.0-85201467266