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    Home > Active Ingredient News > Digestive System Information > In the first-line treatment of liver cancer, Hengrui Pharmaceutical and BeiGene released the latest clinical trial results of ESMO

    In the first-line treatment of liver cancer, Hengrui Pharmaceutical and BeiGene released the latest clinical trial results of ESMO

    • Last Update: 2022-09-21
    • Source: Internet
    • Author: User
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    ▎ WuXi AppTec content team editor

    Hepatocellular carcinoma is the sixth most common type of cancer worldwide, with more than 900,000 new cases in 2020, and more than two-thirds of patients are already in advanced stages of the disease at the time of diagnosis, with only 7% of advanced patients surviving for more than 5 years




    Carellizumab/apatinib reduces risk of disease progression or death by 48%


    In this randomized, open-label, international Phase 3 clinical trial, patients with unresectable hepatocellular carcinoma were randomized to receive carellizumab/apatinib or sorafenib



    The conference summary showed that the median follow-up time was 7.



    In addition, at a median follow-up time of 14.



    Efficacy results of carellizumab/apatinib (C+R) (Image source: Reference[2])


    The researchers said this result showed that the carrelizumab/apatinib combination significantly prolonged progression-free survival and overall survival in patients with unresectable hepatocellular carcinoma compared with the active control



    Terelizumab shows clinically significant overall survival benefit


    In a randomized, open-label, phase 3 global clinical trial called RATIONALE-301, patients with unresectable hepatocellular carcinoma were treated



    The conference summary showed that the median OS of the terelitizumab group was 15.
    9 months at least 33 months of follow-up, and the non-inferiority criterion (HR: 0.
    85) was met compared with the control group (14.
    1 months).


    The objective response rate of Terelizumab was 14.
    3%, which was better than that of the active control group (5.
    4%)
    .

    The median duration of remission was 36.
    1 months in the terelitizumab group and 11.
    0 months
    in the control group.

    In terms of safety, the proportion of adverse events exceeding grade 3 in the tirelizumab group and the adverse events leading to treatment discontinuation were lower than in the active control group
    .

    The researchers said this result shows that terelizumab, as a monotherapy, can provide clinically significant overall survival benefits and has better safety profiles
    .

    More innovative therapies are expected to achieve positive clinical results and bring more treatment options to liver cancer patients
    .


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