echemi logo
Product
  • Product
  • Supplier
  • Inquiry
    Home > Active Ingredient News > Antitumor Therapy > Clin Cancer Res: Cabozantinib and Nivolumab in PCI-Refractory Metastatic Urothelial Carcinoma

    Clin Cancer Res: Cabozantinib and Nivolumab in PCI-Refractory Metastatic Urothelial Carcinoma

    • Last Update: 2022-03-04
    • Source: Internet
    • Author: User
    Search more information of high quality chemicals, good prices and reliable suppliers, visit www.echemi.com

    Metastatic urothelial carcinoma (mUC) is a highly invasive malignancy with high incidence
    .


    Currently, the U.


    FDA

    The aim of this study was to evaluate the efficacy and tolerability of cabozantinib in combination with nivolumab (CaboNivo) in patients with metastatic urothelial carcinoma that has progressed after checkpoint inhibitor therapy
    .

    To evaluate the efficacy and tolerability of cabozantinib in combination with nivolumab (CaboNivo) in patients with metastatic urothelial carcinoma that has progressed on checkpoint inhibitor therapy

    This is a phase I expansion cohort study enrolling patients with mUC who have progressed on prior immune checkpoint inhibitor therapy and are treated with cabozantinib 40 mg/day + nivolumab 3 mg/kg for 2 weeks until Disease progression or unacceptable toxicity
    .


    The primary endpoint was objective response rate


    immunity

    A total of 30 patients were recruited, 29 of whom were evaluable for efficacy
    .


    The median follow-up was 22.


    Alleviate the situation

    Alleviate the situation

    The objective response rate was 16.
    0%, including 1 complete response and 3 partial responses (PR)
    .


    Of the 4 patients who achieved remission on previous checkpoint inhibitor therapy, 2 patients were primary refractory, 1 patient achieved partial response, and 1 patient remained stable


    The objective response rate was 16.


    Progression-Free Survival and Overall Survival

    Progression-Free Survival and Overall Survival

    The median duration of response was 33.
    5 months, the median progression-free survival was 3.
    5 months, and the median overall survival was 10.
    4 months
    .

    The median duration of response was 33.
    5 months, the median progression-free survival was 3.
    5 months, and the median overall survival was 10.
    4 months median duration of response was 33.
    5 months, and the median progression-free survival was 3.
    5 months , the median overall survival was 10.
    4 months

    This research protocol decreased immunosuppressive subsets, such as regulatory T cells (treg), and increased potential antitumor immune subsets, such as atypical monocytes and effector T cells
    .


    At baseline, low percentages of mononuclear myeloid suppressor cells (M-MDSCs) and polymorphonuclear MDSCs, low expression of CTLA-A and TIM-3 on Treg cells, and high levels of CD4+ T cells were associated with better progression-free survival and/or overall survival


    tumor immunity

    In conclusion, cabozantinib combined with nivolumab had good antitumor activity and was well tolerated in patients with metastatic urothelial carcinoma refractory to immune checkpoint inhibitors


    Cabozantinib combined with nivolumab has good antitumor activity in patients with immune checkpoint inhibitor-refractory metastatic urothelial carcinoma, and cabozantinib combined with nivolumab is well tolerated in patients with metastatic urothelial carcinoma.


    Original source:

    Daniel M.


    Cabozantinib plus Nivolumab Phase I Expansion Study in Patients with Metastatic Urothelial Carcinoma Refractory to Immune Checkpoint Inhibitor Therapy Leave a Comment
    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.