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Revisiting Richter transformation in the era of novel CLL agents

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00098892%3A_____%2F21%3AN0000029" target="_blank" >RIV/00098892:_____/21:N0000029 - isvavai.cz</a>

  • Alternative codes found

    RIV/61989592:15110/21:73606360

  • Result on the web

    <a href="https://www.sciencedirect.com/science/article/pii/S0268960X21000308" target="_blank" >https://www.sciencedirect.com/science/article/pii/S0268960X21000308</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.blre.2021.100824" target="_blank" >10.1016/j.blre.2021.100824</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Revisiting Richter transformation in the era of novel CLL agents

  • Original language description

    Richter transformation (RT) is the development of aggressive lymphoma – most frequently diffuse large B-cell lymphoma (DLBCL) and rarely Hodgkin lymphoma (HL) – arising on the background of chronic lymphocytic leukaemia (CLL). Despite recent advances in CLL treatment, RT also develops in patients on novel agents, usually occurring as an early event. RT incidence is lower in CLL patients treated with novel agents in the front line compared to relapsed/refractory cases, with a higher incidence in patients with TP53 disruption. The genetic heterogeneity and complexity are higher in RT-DLBCL than CLL; the genetics of RT-HL are largely unknown. In addition to TP53, aberrations in CDKN2A, MYC, and NOTCH1 are common in RT-DLBCL; however, no distinct RT-specific genetic aberration is recognised yet. RT-DLBCL on ibrutinib is frequently associated with BTK and PLCG2 mutations. Here, we update on genetic analysis, diagnostics and treatment options in RT in the era of novel agents.

  • 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

    30204 - Oncology

Result continuities

  • Project

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2021

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Blood Reviews

  • ISSN

    0268-960X

  • e-ISSN

    1532-1681

  • Volume of the periodical

    49

  • Issue of the periodical within the volume

    September

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    19

  • Pages from-to

    100824

  • UT code for WoS article

    000686765400001

  • EID of the result in the Scopus database

    2-s2.0-85103291631