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Imatinib and pegylated IFN-alfa2b discontinuation in first-line chronic myeloid leukemia patients following a major molecular response.

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61989592%3A15110%2F14%3A33150373" target="_blank" >RIV/61989592:15110/14:33150373 - isvavai.cz</a>

  • Result on the web

    <a href="http://dx.doi.org/10.1111/ejh.12258" target="_blank" >http://dx.doi.org/10.1111/ejh.12258</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1111/ejh.12258" target="_blank" >10.1111/ejh.12258</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Imatinib and pegylated IFN-alfa2b discontinuation in first-line chronic myeloid leukemia patients following a major molecular response.

  • Original language description

    OBJECTIVES: Previous studies indicate that 40-50% of patients with chronic myeloid leukemia in prolonged complete molecular remission may discontinue imatinib therapy without imminent relapse. The combination of pegylated interferon-alpha (Peg-IFN-alfa2b) and imatinib may increase the rate of successful discontinuation. METHODS: In this pilot study, we prospectively stopped imatinib from patients (n = 12) who had achieved major molecular response (MMR) after ?12 months of treatment with either imatinibor imatinib+Peg-IFN-alfa2b. Molecular monitoring was carried out monthly for BCR-ABL1. In addition, analyses of lymphocyte immunophenotype, function, and plasma cytokines were performed. RESULTS: In the monotherapy group, 5/6 patients lost MMR within 4 months. One patient remains to date in MR(4.0) 61 months after discontinuation. In the combination therapy group, 2/6 patients relapsed within 4 months while still receiving Peg-IFN-alfa2b. Four of six patients were able to discontinue bot

  • 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

    <a href="/en/project/NT12218" target="_blank" >NT12218: Personalized treatment of chronic myeloproliferative disorders and myelodysplastic syndrome - a cellular metabolomics study.</a><br>

  • Continuities

    S - Specificky vyzkum na vysokych skolach

Others

  • Publication year

    2014

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    European Journal of Haematology

  • ISSN

    0902-4441

  • e-ISSN

  • Volume of the periodical

    92

  • Issue of the periodical within the volume

    5

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    8

  • Pages from-to

    413-420

  • UT code for WoS article

  • EID of the result in the Scopus database