IDEAS home Printed from https://ideas.repec.org/a/nat/natcom/v15y2024i1d10.1038_s41467-024-53109-4.html
   My bibliography  Save this article

Nivolumab plus anlotinib hydrochloride in advanced gastric adenocarcinoma and esophageal squamous cell carcinoma: the phase II OASIS trial

Author

Listed:
  • Jing Wu

    (Fudan University
    Fudan University
    Shanghai geriatric medical center)

  • Shilong Zhang

    (Fudan University
    Fudan University)

  • Shan Yu

    (Fudan University
    Fudan University)

  • Guo An

    (BGI Genomics
    BGI Genomics)

  • Yi Wang

    (Fudan University)

  • Yiyi Yu

    (Fudan University
    Fudan University)

  • Li Liang

    (Fudan University
    Fudan University)

  • Yan Wang

    (Fudan University
    Fudan University)

  • Xiaojing Xu

    (Fudan University
    Fudan University)

  • YanShi Xiong

    (BGI Genomics
    BGI Genomics)

  • Di Shao

    (BGI Genomics)

  • Zhun Shi

    (BGI Research)

  • Nannan Li

    (BGI Genomics
    BGI Research
    University of Chinese Academy of Sciences)

  • Jingyuan Wang

    (Fudan University
    Fudan University)

  • Dawei Jin

    (BGI Genomics
    BGI Genomics)

  • Tianshu Liu

    (Fudan University
    Fudan University)

  • Yuehong Cui

    (Fudan University
    Fudan University)

Abstract

Vascular endothelial growth factor inhibitors, including tyrosine kinase inhibitors (TKIs), possess immunomodulatory properties and have shown promising outcomes when combined with anti-PD-1 antibodies. The OASIS phase II trial (NCT04503967) is designed to determine the clinical activity and safety of nivolumab (anti-PD-1) and anlotinib hydrochloride (a multi-targets TKI) as second-line or above therapy in patients with advanced gastric adenocarcinoma (GAC) and esophageal squamous cell carcinoma (ESCC). From December 2020 to September 2022, 45 patients with GAC and 3 with ESCC were enrolled in this study. The pre-specified endpoints were reached, with the primary endpoint of overall response rate achieving 29.2%. For secondary objectives, disease control rate was 64.6%; median progression-free survival was 4.0 months; and median overall survival was 11.1 months with a manageable toxicity profile. The exploratory analyses unveiled that the balance of gut bacteria and the presence of a pre-existing immune signature characterized by a high percentage of CD68+PD-L1+ PD-1+ macrophages and low pretreatment variant allele frequencies (VAF), as well as low expression of certain cytokines were significantly associated with improved clinical outcomes in patients with GAC.

Suggested Citation

  • Jing Wu & Shilong Zhang & Shan Yu & Guo An & Yi Wang & Yiyi Yu & Li Liang & Yan Wang & Xiaojing Xu & YanShi Xiong & Di Shao & Zhun Shi & Nannan Li & Jingyuan Wang & Dawei Jin & Tianshu Liu & Yuehong C, 2024. "Nivolumab plus anlotinib hydrochloride in advanced gastric adenocarcinoma and esophageal squamous cell carcinoma: the phase II OASIS trial," Nature Communications, Nature, vol. 15(1), pages 1-15, December.
  • Handle: RePEc:nat:natcom:v:15:y:2024:i:1:d:10.1038_s41467-024-53109-4
    DOI: 10.1038/s41467-024-53109-4
    as

    Download full text from publisher

    File URL: https://www.nature.com/articles/s41467-024-53109-4
    File Function: Abstract
    Download Restriction: no

    File URL: https://libkey.io/10.1038/s41467-024-53109-4?utm_source=ideas
    LibKey link: if access is restricted and if your library uses this service, LibKey will redirect you to where you can use your library subscription to access this item
    ---><---

    More about this item

    Statistics

    Access and download statistics

    Corrections

    All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:nat:natcom:v:15:y:2024:i:1:d:10.1038_s41467-024-53109-4. See general information about how to correct material in RePEc.

    If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.

    We have no bibliographic references for this item. You can help adding them by using this form .

    If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.

    For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: Sonal Shukla or Springer Nature Abstracting and Indexing (email available below). General contact details of provider: http://www.nature.com .

    Please note that corrections may take a couple of weeks to filter through the various RePEc services.

    IDEAS is a RePEc service. RePEc uses bibliographic data supplied by the respective publishers.