echemi logo
Product
  • Product
  • Supplier
  • Inquiry
    Home > Active Ingredient News > Antitumor Therapy > 【CSCO 2022 Preview】CHOICE-01 research promotes precision treatment of lung cancer

    【CSCO 2022 Preview】CHOICE-01 research promotes precision treatment of lung cancer

    • Last Update: 2022-10-31
    • Source: Internet
    • Author: User
    Search more information of high quality chemicals, good prices and reliable suppliers, visit www.echemi.com

    Compared with lung adenocarcinoma, patients with lung squamous cell carcinoma have a worse prognosis and are more challenging
    to treat.
    The rise of immunotherapy has brought new treatment options to patients with lung squam cell carcinoma, because lung squamous cell carcinoma has a higher frequency of somatic mutations and is more immunogenic, and is theoretically more likely to benefit from immunotherapy
    than lung adenocarcinoma.

     

    The CHOICE-01 study (NCT03856411) is the first randomized, double-blind, placebo-parallel-controlled, multicenter phase III clinical study
    in China to include both squamous cell carcinoma and non-squamous cell carcinoma NSCLC patients and anti-PD-1 monoclonal antibody combined with chemotherapy as first-line therapy.

     

    A total of 465 patients with stage III.
    B~IV.
    squamous/non-squamous NSCLC without EGFR/ALK mutation without systematic treatment in 63 centers across the country were randomized 2:1 to receive first-line treatment
    with trepilimab + chemotherapy (309 cases) or placebo + chemotherapy (156 cases).
    Patients in the placebo + chemotherapy group during the period were allowed to continue treatment with trepilimab
    if their disease progressed.

     

    On October 8, 2022, the CHOICE-01 study, led by Professor Wang Jie of the Cancer Hospital of the Chinese Academy of Medical Sciences, was published
    online in the authoritative journal Journal of Clinical Oncology (IF: 50.
    717).

     

    In terms of PFS, the primary endpoint of the CHOICE-01 study, PFS was significantly better in the trepilimab group than in the placebo group (median PFS: 8.
    4 versus 5.
    6 months).

    In terms of secondary endpoint OS, OS was significantly longer in the trepilimab group than in the placebo group [median OS: not reached (NE) vs 17.
    1 months].

    In terms of drug safety, the incidence of grade 3 and above adverse events (AEs) was similar
    in the trepilimab group and the placebo group.

     

    More ingeniously, CHOICE-01 is the first PD-1 monoclonal antibody to use whole exome sequencing (WES) in a large phase III study, and has obtained valuable data, such as FA-PI3K-Akt or IL-7 or SWI/SNF signaling pathway mutations patients are more likely to benefit
    from trepilimab combined chemotherapy.

     

    According to the results of CHOICE-01, the National Medical Products Administration (NMPA) has approved a new indication for the first-line treatment of teruplimab combined with standard chemotherapy for advanced driver gene-negative non-squamous NSCLC, bringing a new option
    to Chinese patients.
    It is believed that there will be more opportunities to obtain more data in the real world in the future to further verify the value of
    the above biomarkers.

     

    On November 9, 2022, Professor Chu Tianqing of the Department of Respiratory Medicine of Shanghai Jiao Tong University Chest Hospital will introduce the latest interpretation of the CHOICE-01 study at the CSCO 2022 Annual Conference, which has a long way to overcome lung cancer, and many Chinese doctors are seeking
    to do so.
    It is believed that in the future, more Chinese forces will emerge from precision immunotherapy for lung cancer to benefit the majority of patients!

     

    Resources:

    https://mp.
    weixin.
    qq.
    com/s/ECDNKjHVRDNsVy8n0ohQkw

    https://mp.
    weixin.
    qq.
    com/s/Q5sJpSMpG5oyYxjgudkw_w

    https://mp.
    weixin.
    qq.
    com/s/_WbwSnM3EeOwVZWQIsbpNg

    https://mp.
    weixin.
    qq.
    com/s/BtA15kwZn3_XtHsRxgMQaw

     

    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.