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    Home > Active Ingredient News > Antitumor Therapy > Lancet sub-journal: Karelli pearl single anti-scale non-scale NSCLC maximum total lifetime

    Lancet sub-journal: Karelli pearl single anti-scale non-scale NSCLC maximum total lifetime

    • Last Update: 2021-01-14
    • Source: Internet
    • Author: User
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    For patients with advanced non-squamous non-small cell lung cancer (NSCLC) without EGFR or ALC mutations, immunotherapy in combination with chemotherapy is the most common and effective treatment.
    but there is a lack of evidence in the Asian population.
    December 18, the study published in the Lancet sub-journal published the clinical trial data of China Hengrui Pharmaceuticals' independent research and development of PD-1 camrelizumab in combination with permeable curvature compared with chemotherapy alone in patients with advanced non-scaly NSCLC.
    random, open label, multi-center, Phase 3 clinical trial (CamelL) led by Shanghai Lung Hospital, carried out in 52 hospitals in China.
    a total of 419 patients were included between 2017.5.12 and 2018.6,6, of whom 417 non-scale NSCLC patients without EGFR ALC mutation were randomly divided into two groups for treatment: carelli's single-anti-combination chemotherapy (carbaptin-pemonics) or individual chemotherapy.
    end events are progress-free survival (PFS) in all patients and in patients with positive PD-L1.
    of the events was the total survival of the patient and the oncology imaging assessment that was not conducted for 6-12 weeks.
    -term analysis, the medium follow-up time was 11.9 months.
    compared to the individual chemotherapy group, the mid-level PFS in the combined treatment group was significantly extended (11.3 vs. 8.3 months, HR=0.60), and the risk of disease progression or patient death was reduced by 40%, reaching the main focus event of the study.
    PFS with two groups of patients.
    When the PD-L1 tumor ratio score was further analyzed as a covariate ≥, it was found that the combined treatment group still had PFS higher than the chemotherapy group leader (HR-0.62), with 49.6% and 35.1% of patients in the two groups reaching the 12-month PFS target, respectively.
    , in the patient subgroup with a PD-L1 tumor ratio score of ≥1%, the combined treatment group reduced the patient's risk of progression or death by 44% (medium PFS 15.4 months vs 9.9 months).
    the mid-term analysis, a total of 143 patients died.
    K-M curve analysis showed that the joint group increased the total survival of the patients in the middle (OR did not reach vs 20.9 months, HR s 0.73).
    12-month total survival of the combined treatment group and the chemotherapy group was 74.9% and 67.1%, respectively.
    the mixed factors, it was found that combined therapy improved patient survival by 39%.
    total survival time K-M curve.
    The most common treatment-related adverse events in this trial were a decrease in the number of neutral granulocytes (combined treatment group vs chemotherapy group: 38% vs 30%), a decrease in white blood cell count (20% vs 14%), anemia (19% vs 11%) and a decrease in plateplate count (17% vs 12%).
    , 74 (36%) and 27 (13%) patients were reported in both groups;
    the results prove that the total survival of the advanced non-scale NSCLC in the first-line treatment of Karelli's mono-anti-combination chemotherapy was 27.9 months, the researchers noted.
    data is the world's longest survival benefit data in clinical studies of immunotherapy for lung cancer, successfully breaking the two-year mark.
    also marks that China's lung cancer immunotherapy is enough to meet the international leading level.
    , the drug was approved by China's National Drug Administration (NMPA).
    : Caicun Zhou, et al., (2020). Camrelizumab plus carboplatin and pemetrexed versus chemotherapy alone in chemotherapy-naive patients with advanced non-squamous non-small-cell lung cancer (CameL): a randomised, open-label, multicentre, phase 3 trial. The Lancet Health Medicine, DOI: MedSci Original Source: MedSci Original Copyright Notice: All text, images and audio and video materials on this website that indicate "Source: Met Medical" or "Source: MedSci Original" are owned by Mets Medicine and are not authorized to reproduce by any media, website or individual, and must be reproduced with the words "Source: Met Medical".
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