echemi logo
Product
  • Product
  • Supplier
  • Inquiry
    Home > Active Ingredient News > Antitumor Therapy > Clin Cancer Res: Early use of high-dose hormones to manage irAE is associated with poor prognosis of anti-PD-1 monotherapy for advanced melanoma

    Clin Cancer Res: Early use of high-dose hormones to manage irAE is associated with poor prognosis of anti-PD-1 monotherapy for advanced melanoma

    • Last Update: 2021-08-26
    • Source: Internet
    • Author: User
    Search more information of high quality chemicals, good prices and reliable suppliers, visit www.echemi.com

    Programmed cell death receptor-1 (PD-1) inhibitors are the first-line treatment for advanced melanoma
    .


    Severe immune- related adverse reactions (ieAE) usually require glucocorticoid (GCC) immunosuppressive therapy


    immunity

    This is a multicenter retrospective analysis that included patients treated with anti-PD-1 monoclonal therapy from 2009 to 2019, and collected detailed GCC use data from five independent cohorts
    .


    The median follow-up time was 206 weeks


    PFS of two groups of patients in the MGH cohort and validation cohort

    PFS of two groups of patients in the MGH cohort and validation cohort

    Of the 947 patients in the total cohort, 509 (54%) patients had an irAE
    .


    In the MGH cohort (irAE[+]n=90), early-onset irAE (anti-PD-1 treatment ) with high-dose GCC (≥60 mg, prednisone) was used compared with irAE without early use of high-dose GCC Within the first 8 weeks after irAE ) was independently associated with poorer PFS and OS after irAE (PFS after irAE: HR 5.


    Compared with irAEs that did not use high-dose GCC early, compared with irAEs that did not use high-dose GCC early, the early-onset irAEs of early-onset irAEs that used high-dose GCC had higher PFS and OS after irAE.
    Poor independent correlation is associated with poor PFS and OS after irAE

    OS of two groups of patients in MGH cohort and validation cohort

    OS of two groups of patients in MGH cohort and validation cohort

    The above research results were confirmed in the combined validation cohort (irAE[+]n=419, PFS after irAE: HR1.
    69, 95%CI 1.
    04-2.
    76, p=0.
    04; OS: HR 1.
    97, 95%CI 1.
    15-3.
    39 , p=0.
    01)
    .


    In addition, in the 26-week important analysis of PFS after irAE, similar results were observed, but similar results were not observed in the 26-week analysis of OS after irAE


    In summary, after the occurrence of irAE, early use of high-dose GCC is associated with poor PFS and OS prognosis
    .


    In the process of anti-PD-1 monotherapy, GCC should be used more rationally


    After the occurrence of irAE, early use of high-dose GCC is associated with poor PFS and OS prognosis After irAE occurs, early use of high-dose GCC is associated with poor PFS and OS prognosis

    Original source:

    Original source:

    Xue Bai, Jiani Hu, Allison Betof Warner, et al.


    Early use of high-dose-glucocorticoid for the management of irAE is associated with poorer survival in patients with advanced melanoma treated with monotherapy anti-PD-1 in this message
    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.