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    Home > Active Ingredient News > Blood System > JCO: Final analysis results of Ixazomi combined with lenalidomide + dexamethasone in the treatment of relapsed or refractory multiple myeloma (RRMM): Phase III clinical study TOURMALINE-MM1

    JCO: Final analysis results of Ixazomi combined with lenalidomide + dexamethasone in the treatment of relapsed or refractory multiple myeloma (RRMM): Phase III clinical study TOURMALINE-MM1

    • Last Update: 2021-06-21
    • Source: Internet
    • Author: User
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    The TOURMALINE-MM1 study is a global multicenter, double-blind, placebo-controlled randomized phase III study that evaluates Ixazomib combined with lenalidomide + dexamethasone (Ixazomib-Rd) versus placebo combined with lenalidomide + dexamethasone (Placebo-Rd) Efficacy and safety in relapsed or refractory (RR) multiple myeloma (MM)


    The TOURMALINE-MM1 study is a global multicenter, double-blind, placebo-controlled randomized phase III study that evaluates Ixazomib combined with lenalidomide + dexamethasone (Ixazomib-Rd) versus placebo combined with lenalidomide + dexamethasone (Placebo-Rd) Efficacy and safety in relapsed or refractory (RR) multiple myeloma (MM)


    There were 360 ​​patients in the Ixazomib-Rd group and 362 patients in the placebo-Rd group


    There were 360 ​​patients in the Ixazomib-Rd group and 362 patients in the placebo-Rd group


    In subgroup analysis, it was found that Ixazomib-Rd has a tendency to benefit in some subgroups, such as refractory after any line treatment (HR=0.



    OS for two groups and subgroups analysis

    For the following patients , Ixazomib-Rd treatment has achieved a numerical benefit of OS, patients with del(17p) (HR=0.


    For the following patients , Ixazomib-Rd treatment has achieved a numerical benefit of OS, patients with del(17p) (HR=0.



    OS with different genetic risks

    In the two groups, 259 patients (71.


    In the two groups, 259 patients (71.


    The median OS of the two groups who received the posterior protease inhibitor was 52.



    OS in the two groups that received or did not receive late-line protease inhibitors

    During the 7-year follow-up period, no new or additional safety incidents occurred


    During the 7-year follow-up period, no new or additional safety incidents occurred



    Adverse events

    In summary, the progression-free survival (PFS) benefit of Ixazomib-Rd in the treatment of relapsed or refractory multiple myeloma (RRMM) does not translate into the benefit of OS
    .
    However, in some subgroups, the Ixazomib-Rd group has a tendency to benefit from OS
    .

    In summary, the progression-free survival (PFS) benefit of Ixazomib-Rd in the treatment of relapsed or refractory multiple myeloma (RRMM) does not translate into the benefit of OS
    .
    However, in some subgroups, the Ixazomib-Rd group has a tendency to benefit from OS
    .
    The progression-free survival (PFS) benefit of Ixazomib-Rd in the treatment of relapsed or refractory multiple myeloma (RRMM) did not translate into the benefit of OS
    .
    However, in some subgroups, the Ixazomib-Rd group has a tendency to benefit from OS
    .
    The progression-free survival (PFS) benefit of Ixazomib-Rd in the treatment of relapsed or refractory multiple myeloma (RRMM) did not translate into the benefit of OS
    .
    However, in some subgroups, the Ixazomib-Rd group has a tendency to benefit from OS
    .

    Original source:

    Original source:

    Paul G Richardson, Shaji K Kumar, Tamás Masszi, et al.
    Final Overall Survival Analysis of the TOURMALINE-MM1 Phase III Trial of Ixazomib, Lenalidomide, and Dexamethasone in Patients With Relapsed or Refractory Multiple Myeloma.
    J Clin Oncol.
    2021 Jun 11; JCO2100972.
    doi: 10.
    1200/JCO.
    21.
    00972.
    Online ahead of print.

    Paul G Richardson, Shaji K Kumar, Tamás Masszi, et al.
    Final Overall Survival Analysis of the TOURMALINE-MM1 Phase III Trial of Ixazomib, Lenalidomide, and Dexamethasone in Patients With Relapsed or Refractory Multiple Myeloma.
    J Clin Oncol.
    2021 Jun 11; JCO2100972.
    doi: 10.
    1200/JCO.
    21.
    00972.
    Online ahead of print.


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