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    Home > Active Ingredient News > Antitumor Therapy > Blood: efficacy and safety of Cilta-cel in patients with progressive multiple myeloma

    Blood: efficacy and safety of Cilta-cel in patients with progressive multiple myeloma

    • Last Update: 2022-09-30
    • Source: Internet
    • Author: User
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    B-cell mature antigen (BCMA)-targeted therapies, including bispecific antibodies (BsAbs) and antibody-drug conjugates (ADCs), are promising treatments for multiple myeloma (MM), but the disease may progress
    after use.

    CARTITUDE-2 is a Phase 2 multi-cohort study evaluating the efficacy and safety of Cilta-cel, an anti-BCMA chimeric antigen receptor T cell therapy, in a variety of myeloma patient populations
    .

    Patients in Cohort C progressed
    despite proteasome inhibitors, immunomodulatory drugs, anti-CD38 antibodies, and noncellular anti-BCMA immunotherapy.
    A single Cilta-cel infusion
    is given after lymphatic failure.
    The primary endpoint was negative for minimal residual disease (MRD) (10-5
    ).

    Overall, 20 patients were treated in the study (13 ADC exposed, 7 BsAb exposed, and 1 had previous BsAb exposure in the ADC group
    ).
    Sixteen (80%) patients were refractory
    to previous anti-BCMA therapy.


    Progression-free survival rate across the cohort

    At a median follow-up of 11.



    Occurrence of adverse reactions

    The most common adverse reactions are blood
    .


    In summary, Cilta-cel induces good responses in patients with relapsed/refractory multiple myeloma who have previously received anti-BCMA therapy and have exhausted other treatments
    .


    Original Source:

    Cohen Adam D,Mateos Maria-Victoria,Cohen Yael C et al.


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