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    Home > Active Ingredient News > Antitumor Therapy > Phase III study of tiragolumab combined with atezolizumab in extensive-stage small cell lung cancer failed (SKYSCRAPER-02 study)

    Phase III study of tiragolumab combined with atezolizumab in extensive-stage small cell lung cancer failed (SKYSCRAPER-02 study)

    • Last Update: 2022-04-23
    • Source: Internet
    • Author: User
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    The 5-year average survival rate of non-small cell lung cancer ( NSCLC ) patients is about 15%, and more than 70% of NSCLC patients are diagnosed at an advanced stage that is not suitable for conventional chemoradiotherapy
    .


    In recent years, a series of breakthroughs have been made in tumor immunotherapy .


    The 5-year average survival rate of non-small cell lung cancer ( NSCLC ) patients is about 15%, and more than 70% of NSCLC patients are diagnosed at an advanced stage that is not suitable for conventional chemoradiotherapy


    At present, a number of PD-1/PD-L1 monoclonal antibodies have been approved worldwide, including Nivolumab, Atezolizumab, Avelumab and duvalumab Durvalumab has shown promising efficacy


    TIGIT (T cell immunoreceptor with Ig and ITIM domains), the full name of T cell immunoglobulin and ITIM domain protein, is a novel immune checkpoint inhibitory receptor that exists in activated T cells in various cancers including NSCLC.


    Tiragolumab is a monoclonal antibody and the world's first TIGIT antibody to be promoted to Phase III clinical trials


    Tecentriq (Atezolizumab) is a monoclonal antibody and the first PD-L1 inhibitor approved by the FDA for clinical treatment of tumors


    Dual immune checkpoint inhibitor combination therapy concept

    The previous Phase 1 and Phase 2 clinical studies have achieved satisfactory results
    .


    Phase 2 study CITYSCAPE 01 is a prospective, randomized, double-blind, placebo-controlled Phase II trial evaluating tiragolumab + atezolizumab (TA) versus placebo + atezolizumab (PA) in first-line treatment of advanced stage Efficacy and safety in patients with NSCLC


    The previous Phase 1 and Phase 2 clinical studies have achieved satisfactory results


    A phase 3 clinical trial was carried out for this purpose


    Regrettably, on March 30 this year, this clinical trial failed to meet the co-primary endpoint of progression-free survival (PFS) , nor did it meet the co-primary endpoint of overall survival(OS) in the interim analysis , and at the end of the program Statistical significance is unlikely to be reached in the analysis
    .

    Regrettably, on March 30 this year, this clinical trial failed to meet the co-primary endpoint of progression-free survival (PFS) , nor did it meet the co-primary endpoint of overall survival(OS) in the interim analysis , and at the end of the program Statistical significance is unlikely to be reached in the analysis
    .


    statistics

    About TIGIT

    About TIGITAbout TIGIT

    TIGIT stands for T cell immunoglobulin and ITIM domain protein (T cell immunoreceptor with Ig and ITIM domains), which is also an inhibitory receptor expressed on the surface of various types of T cells and NK cells
    .


    Tiragolumab is a fully human IgG1/kappa anti-TIGIT monoclonal antibody with an intact Fc region that blocks the binding of TIGIT to its ligand PVR and co-activating receptor CD226, theoretically restoring anti-tumor responses and enhancing anti-PD -L1 antibody efficacy


    Tiragolumab is one of Roche's next-generation immune checkpoint inhibitors, and SKYSCRAPER-02 is one of five Phase III trials Roche has conducted for tiragolumab
    .


    At the same time, SCLC is a type of lung cancer with a high degree of malignancy, and many drugs with different mechanisms have also been broken into sand


    Data from the SKYSCRAPER-02 study will be presented at a later medical meeting, but in general, the TIGIT target has not played a role in "sweeping the ground
    .
    " After PD-1/L1 immunotherapy, we need to solve how to expand the benefit population of immunotherapy, especially the new therapy in PD-1/L1 treatment non-responder or intolerant population.
    It seems that TIGIT and LAG3 do not currently show Such potential
    .

    After PD-1/L1 immunotherapy, the industry has been exploring new immunotherapies, and TIGIT is one of the most popular targets, attracting international giants such as Roche, Gilead, Merck, Novartis, etc.
    Development of specific dual-antibody therapy based on TIGIT
    .

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