echemi logo
Product
  • Product
  • Supplier
  • Inquiry
    Home > Biochemistry News > Biotechnology News > The first-line treatment of esophageal cancer Keytruda combination therapy was eligible for FDA priority review

    The first-line treatment of esophageal cancer Keytruda combination therapy was eligible for FDA priority review

    • Last Update: 2020-12-31
    • Source: Internet
    • Author: User
    Search more information of high quality chemicals, good prices and reliable suppliers, visit www.echemi.com
    Esophageal cancer is a type of cancer that is difficult to treat and begins in the inner layer of the esophageal (mucous membrane) and grows outwards.
    main types of esophageal cancer are squamous cell carcinoma and adenocarcinoma.
    esophageal cancer is the seventh most common cancer and sixth leading cause of death in the world.
    estimates that there will be more than 572,000 new cases of esophageal cancer diagnosed globally in 2018, with nearly 509,000 deaths from the disease.
    , it is the fourth leading cause of cancer death in China, after lung, stomach and liver cancers.
    high incidence of esophageal cancer in China may be related to China's "hot eating" diet.
    this sBLA is based on the positive results of key Phase 3 clinical trial KEYNOTE-590.
    In this trial, Keytruda's combination therapy with chemotherapy significantly improved the patient's total and non-progressed survival compared to chemotherapy, regardless of whether the patient's tumor expressed PD-L1 and the tumor histological characteristics.
    interim analysis presented at this year's ESMO Conference showed that Keytruda combined therapy reduced the risk of death by 27% compared to chemotherapy at a medium follow-up time of 10.8 months (HR=0.73,95% CI, 0.62-0.86, p-lt;0.0001).
    total survival (OS) in patients reached 12.4 months, and in the chemotherapy group it was 9.8 months.
    Keytruda combination therapy in KETNOTE-590 clinical trial lifetime data (Photo: Mercadon.com) It is worth noting that in the Asian patient sub-group, this combination therapy showed better outcomes than the entire patient population, reducing the risk of death by 36% (HR=0.64) and the risk of disease progression or death by 41% (HR=0.59).
    : .1) FDA Grants Grants Review to Merck's Supplemental Biologics License Application for KEYTRUDA® (pembrolizumab) Plus Filmy as First-Treatment Line for Locally Advanced Unresectable or Metastatic Esophageal and Gastroesophal Junction. Retrieved December 17, 2020, from。
    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.