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    Home > Active Ingredient News > Antitumor Therapy > Clin Cancer Res: Activity and safety of α-PD-L1 antibody ± α-TIM-3 antibody in the treatment of MSI-H/dMMR tumors

    Clin Cancer Res: Activity and safety of α-PD-L1 antibody ± α-TIM-3 antibody in the treatment of MSI-H/dMMR tumors

    • Last Update: 2021-09-11
    • Source: Internet
    • Author: User
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    Immune checkpoint inhibitors show high response rates and long-lasting clinical benefits in tumors with microsatellite instability-high/mismatch repair defects (MSI-H/dMMR)


    immunity

    This is a phase 1b clinical trial to evaluate the safety and anti-tumor activity of anti-PD-L1 antibody LY3300054 as a single agent or in combination with anti-TIM-3 antibody LY3321367 in patients with advanced solid tumors of MSI-H/dMMR


    Enrolled 18-year-old patients with solid tumors who have not previously received anti-PD-1/PD-L1 therapy, and were treated with LY3300054 as a single agent (n=40) or combined with LY3321367 (n=20); for PD-1/PD -L1 inhibitor-resistant/refractory tumor patients received combination therapy (n=22)


    A total of 82 patients were recruited, the most being colorectal tumors (n=39, 47.


    The occurrence of TRAE in the two groups

    The occurrence of TRAE in the two groups

    The incidence of treatment-related adverse events (TRAE) in the single-drug cohort, PD-1/PD-L1 inhibitor-initial combined cohort, and PD-1/PD-L1 inhibitor-resistant/refractory combined cohort were respectively 55.


    The incidence of treatment-related adverse events (TRAE) in the single-drug cohort, PD-1/PD-L1 inhibitor-initial combined cohort, and PD-1/PD-L1 inhibitor-resistant/refractory combined cohort were respectively 55.


    Various efficacy evaluation results of the two groups

    Various efficacy evaluation results of the two groups

    The objective response rates of the single-drug cohort, PD-1/PD-L1 inhibitor-initial combined cohort, and PD-1/PD-L1 inhibitor resistant/refractory combined cohort were 32.


    The objective response rates of the single-drug cohort, PD-1/PD-L1 inhibitor-initial combined cohort, and PD-1/PD-L1 inhibitor resistant/refractory combined cohort were 32.


    Both LY3300054 monotherapy and LY3300054/anti-TIM-3 combination therapy have controllable safety


    Original source:

    Antoine Hollebecque, et al.


    Safety and antitumor activity of α-PD-L1 antibody as monotherapy or in combination with α-TIM-3 antibody in patients with microsatellite instability-high/mismatch repair-deficient tumors.


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