An exploratory clinical study of β-glucan combined with camrelizumab and SOX chemotherapy as first-line treatment for advanced gastric adenocarcinoma

Front Immunol. 2024 Aug 26:15:1448485. doi: 10.3389/fimmu.2024.1448485. eCollection 2024.

Abstract

Background: β-glucan has been reported to be a potential natural immune modulator for tumor growth inhibition. We aimed to evaluate the efficacy and safety of β-glucan plus immunotherapy and chemotherapy in the first-line treatment of advanced gastric adenocarcinoma.

Methods: This is a phase IB, prospective, single-arm, investigator-initiated trail. Advanced gastric adenocarcinoma patients received β-glucan, camrelizumab, oxaliplatin, oral S-1 every 3 weeks. The curative effect was evaluated every 2 cycles. The primary endpoints were objective response rate (ORR) and safety, with secondary endpoints were median progression-free survival (mPFS) and median overall survival (mOS). The exploratory endpoint explored biomarkers of response to treatment efficacy.

Results: A total of 30 patients had been enrolled, including 20 (66.7%) males and all patients with an ECOG PS score of ≥1. The ORR was 60%, the mPFS was 10.4 months (95% confidence interval [CI], 9.52-11.27), the mOS was 14.0 months (95% CI, 11.09-16.91). A total of 19 patients (63.3%) had TRAEs, with 9 patients (30%) with grade ≥ 3. The most common TRAEs were nausea (53.3%). After 2 cycles of treatment, the levels of IL-2, IFN-γ and CD4+ T cells significantly increased (P < 0.05). Furthermore, biomarker analysis indicated that patient with better response and longer OS exhibited lower GZMA expression at baseline serum.

Conclusions: This preliminary study demonstrates that β-glucan plus camrelizumab and SOX chemotherapy offers favorable efficacy and a manageable safety profile in patients with advanced gastric adenocarcinoma, and further studies are needed to verify its efficacy and safety.

Clinical trial registration: Chinese Clinical Trials Registry, identifier ChiCTR2100044088.

Keywords: camrelizumab; chemotherapy; first-line; gastric cancer; β-glucan.

Publication types

  • Clinical Trial, Phase I

MeSH terms

  • Adenocarcinoma* / drug therapy
  • Adenocarcinoma* / mortality
  • Adult
  • Aged
  • Antibodies, Monoclonal, Humanized* / administration & dosage
  • Antibodies, Monoclonal, Humanized* / adverse effects
  • Antibodies, Monoclonal, Humanized* / therapeutic use
  • Antineoplastic Combined Chemotherapy Protocols* / adverse effects
  • Antineoplastic Combined Chemotherapy Protocols* / therapeutic use
  • Drug Combinations
  • Female
  • Humans
  • Male
  • Middle Aged
  • Oxaliplatin* / administration & dosage
  • Oxaliplatin* / adverse effects
  • Oxaliplatin* / therapeutic use
  • Oxonic Acid / administration & dosage
  • Oxonic Acid / adverse effects
  • Oxonic Acid / therapeutic use
  • Prospective Studies
  • Stomach Neoplasms* / drug therapy
  • Stomach Neoplasms* / mortality
  • Tegafur / administration & dosage
  • Tegafur / adverse effects
  • Tegafur / therapeutic use
  • Treatment Outcome
  • beta-Glucans* / administration & dosage
  • beta-Glucans* / therapeutic use

Substances

  • camrelizumab
  • Antibodies, Monoclonal, Humanized
  • beta-Glucans
  • Oxaliplatin
  • Oxonic Acid
  • Tegafur
  • Drug Combinations
  • S 1 (combination)

Grants and funding

The author(s) declare financial support was received for the research, authorship, and/or publication of this article. This work was supported by the Key Project of Jiangsu S &T Plan (BE2023693), Jiangsu Provincial Health Commission (ZD2022035).