echemi logo
Product
  • Product
  • Supplier
  • Inquiry
    Home > Active Ingredient News > Antitumor Therapy > ESMO Open: A first-line regimen of paclitaxel combined with carboplatin plus bevacizumab for the treatment of recurrent/metastatic nasopharyngeal carcinoma

    ESMO Open: A first-line regimen of paclitaxel combined with carboplatin plus bevacizumab for the treatment of recurrent/metastatic nasopharyngeal carcinoma

    • Last Update: 2021-12-04
    • Source: Internet
    • Author: User
    Search more information of high quality chemicals, good prices and reliable suppliers, visit www.echemi.com

    So far, the value of anti- angiogenic antibody therapy in recurrent or metastatic nasopharyngeal carcinoma (R/M NPC) is still unclear
    .


    Professor Huang Yan from the Department of Oncology, Sun Yat-sen University Cancer Center led his team and partners to conduct a phase 2 clinical trial to evaluate the feasibility of paclitaxel combined with carboplatin plus bevacizumab in the treatment of recurrent or metastatic nasopharyngeal carcinoma Sex


    Blood vessel

    A total of 80 untreated patients with recurrent/metastatic nasopharyngeal carcinoma were recruited and randomly (1:1) divided into two groups to receive paclitaxel (175 mg/m2) combined with carboplatin + bevacizumab (CPB group) ) Or paclitaxel combined with carboplatin (CP group) for up to 6 consecutive courses
    .


    The primary endpoint is the progression-free survival (PFS) assessed by the investigator, and the secondary endpoints are the progression-free survival, overall survival (OS), objective response rate (ORR), and safety assessed by the independent committee


    Progression-free survival in both groups

    Progression-free survival in both groups

    The median progression-free survival estimated by investigators in the CPB group and CP group were 7.
    5 months (95% CI 6.
    53-8.
    45) and 6.
    5 months (95% CI 5.
    53-7.
    52; P=0.
    0148), respectively.
    The progression survival period is similar to this
    .


    The median overall survival of CPB group and CP group was also similar (21.


    The tumor shrinkage rate of the CPB group was significantly higher than that of the CP group .


    Overall survival of the two groups

    Overall survival of the two groups

    There was no significant difference in adverse events of grade 3 and above between the two groups
    .

    In summary, in the first-line regimen of paclitaxel combined with carboplatin, the addition of bevacizumab cannot prolong the progression-free survival and overall survival of patients with recurrent or metastatic nasopharyngeal carcinoma, but it can increase the tumor shrinkage rate.

    .


    The results of this study suggest that bevacizumab combined with chemotherapy may be used as an alternative for nasopharyngeal carcinoma with large tumor volume or seeking short-term effects of neoadjuvant chemotherapy and concurrent chemotherapy


    In the first-line regimen of paclitaxel combined with carboplatin, the addition of bevacizumab cannot prolong the progression-free survival and overall survival of patients with recurrent or metastatic nasopharyngeal carcinoma, but it can increase the tumor shrinkage rate


    Original source:

    Zhou T,Yang Y,Ma S et al.


    Bevacizumab versus placebo in combination with paclitaxel and carboplatin as first-line treatment for recurrent or metastatic nasopharyngeal carcinoma: a multicentre, randomised, open-label, phase II tria 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.