echemi logo
Product
  • Product
  • Supplier
  • Inquiry
    Home > Active Ingredient News > Digestive System Information > Express first-line treatment of liver cancer, dual immune combination therapy reduces risk of death by 22%

    Express first-line treatment of liver cancer, dual immune combination therapy reduces risk of death by 22%

    • Last Update: 2022-02-22
    • Source: Internet
    • Author: User
    Search more information of high quality chemicals, good prices and reliable suppliers, visit www.echemi.com
    ▎WuXi AppTec content team editor Today, AstraZeneca announced that the blockbuster PD-L1 inhibitor durvalumab (durvalumab, English brand name: Imfinzi) combined with the anti-CTLA-4 antibody tremelimumab, Significantly prolongs overall survival in patients with unresectable hepatocellular carcinoma in a phase 3 clinical trial compared to active controls
    .

    Liver cancer is the sixth most common cancer in the world, with approximately 900,000 patients diagnosed each year
    .

    It is also the third leading cause of cancer death, with only about 7% of advanced patients surviving more than 5 years
    .

    Imfinzi is an anti-PD-L1 monoclonal antibody that relieves tumor cells from suppressing immune responses by blocking the binding of PD-L1 to PD-1 and CD80 proteins
    .

    It has been approved in several countries and regions for the treatment of extensive-stage small cell lung cancer
    .

    It is also FDA-approved for the treatment of non-small cell lung cancer and advanced bladder cancer
    .

    Tremelimumab blocks the activity of CTLA-4, which promotes T cell activation and stimulates the immune system's immune response to cancer
    .

    It was used in combination with Imfinzi and chemotherapy to significantly improve patients' overall survival in a Phase 3 clinical trial in first-line treatment of stage IV non-small cell lung cancer
    .

    In the phase 3 clinical trial, called HIMALAYA, patients first received a combination of tremelimumab and Imfinzi once, and then received Imfinzi as a monotherapy every 4 weeks
    .

    This dosing regimen is designed to stimulate T cell activation while reducing the toxic side effects of CTLA-4 antibodies
    .

    The trial results showed that patients treated with this dosing regimen had a 22% lower risk of death compared with the active control group (HR=0.
    78, 96.
    02% CI 0.
    65-0.
    93, p=0.
    0035)
    .

    The median overall survival was 16.
    4 months and 13.
    8 months in the active control group
    .

    About 31 percent of patients were still alive three years after treatment, compared with 20 percent in the control group
    .

    The objective response rate for the combination of tremelimumab and Imfinzi was 20.
    1%, compared with 5.
    1% in the control group
    .

    See the table below for detailed data: Image source: Reference[1] Dr Susan Galbraith, Executive Vice President, Oncology R&D, AstraZeneca, said: "The HIMALAYA trial confirms our strategy of using tremelimumab to exploit the potential to inhibit CTLA-4 and utilize A unique dosing regimen to stimulate the immune system, help patients live longer, and reduce side effects
    .

    We look forward to bringing potential new treatment options to patients with unresectable liver cancer as soon as possible, an area of ​​high unmet need
    .

    "Reference: [1] Imfinzi plus tremelimumab demonstrated unprecedented survival in 1st-line unresectable liver cancer with 31% of patients alive at three years.
    Retrieved January 18, 2022, from https:// /media-centre/press-releases/2022/imfinzi-plus-tremelimumab-unprecedented-survival-1st-line-unresectable-liver-cancer.
    htmlDisclaimer: WuXi AppTec content team focuses on global biomedical health research
    progress.
    This
    article For the purpose of information exchange only, the opinions in this article do not represent WuXi AppTec's position, nor do they represent WuXi AppTec's support or opposition to the opinions in the article
    .

    This article is not a treatment plan recommendation
    .

    If you need treatment plan guidance, please go to a regular hospital for treatment
    .

    This article is an English version of an article which is originally in the Chinese language on echemi.com and is provided for information purposes only. This website makes no representation or warranty of any kind, either expressed or implied, as to the accuracy, completeness ownership or reliability of the article or any translations thereof. If you have any concerns or complaints relating to the article, please send an email, providing a detailed description of the concern or complaint, to service@echemi.com. A staff member will contact you within 5 working days. Once verified, infringing content will be removed immediately.

    Contact Us

    The source of this page with content of products and services is from Internet, which doesn't represent ECHEMI's opinion. If you have any queries, please write to service@echemi.com. It will be replied within 5 days.

    Moreover, if you find any instances of plagiarism from the page, please send email to service@echemi.com with relevant evidence.