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    Home > Active Ingredient News > Blood System > J Clin Oncol: Ibrutinib combined with Venetog as the first-line treatment of chronic lymphocytic leukemia has a good prognosis

    J Clin Oncol: Ibrutinib combined with Venetog as the first-line treatment of chronic lymphocytic leukemia has a good prognosis

    • Last Update: 2021-10-20
    • Source: Internet
    • Author: User
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    Ibrutinib, a BTK inhibitor, is also the only one that has been proven to simultaneously improve the progression-free survival of patients with previously untreated CLL or small lymphocytic lymphoma compared with standard chemotherapy and/or immunochemotherapy ( PFS) and overall survival (OS) targeted therapy .


    Immune lymphoma

    The randomized Phase 2 CAPTIVATE (NCT02910583) study evaluated the efficacy and safety of ibrutinib combined with Venetog as first-line treatment in CLL patients


    In this study, previously untreated CLL patients under 70 years of age received three courses of ibrutinib + 12 courses of ibrutinib combined with Venetog


    Availability of uMRD

    Availability of uMRD

    A total of 164 patients entered three courses of ibrutinib treatment


    After 12 courses of ibrutinib + venetol, the best uMRD remission rate was 75% (peripheral blood) and 68% (bone marrow)


    1-year PFS rate of patients in the placebo group and ibrutinib group

    Among the patients whose tumors were decimated after the initial 3 courses of ibrutinib treatment, 36 (90%) of 40 patients with a high risk of tumor lysis syndrome at baseline converted to medium or low tumor lysis syndrome Levy risk category


    In summary, Ibrutinib combined with Venetog can achieve a higher remission rate as a first-line treatment for CLL


    Ibrutinib combined with Venetog can obtain a higher remission rate as the first-line treatment of CLL


    Original source:

    William G.


    Ibrutinib Plus Venetoclax for First-Line Treatment of Chronic Lymphocytic Leukemia: Primary Analysis Results From the Minimal Residual Disease Cohort of the Randomized Phase II CAPTIVATE Study

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