A Study on the Efficacy of Sodium Propionate Combined With Anti-PD-1 Immunotherapy in Gastric Cancer

NCT07615907 — Not applicable, Not yet recruiting, 20 participants, Jinling Hospital, China

ClinicalTrials Daily  ·  Areas  ·  Conditions  ·  Drugs  ·  Sponsors  ·  

Sodium Propionate Combined With Anti-PD-1 Immunotherapy on Tumor Efficacy in Gastric Cancer Patients

RegistryNCT07615907, acronym PAPGC
StatusNot yet recruiting
PhaseNot applicable
Study typeInterventional; randomized, parallel, masking: single, treatment
Enrollment20 (Estimated)
SponsorJinling Hospital, China (Other)
ConditionsGastric Cancer (GC)
InterventionsSodium propionate (Dietary supplement)
Datesstart 2026-05-30 (estimated), primary completion 2026-08-30 (estimated), completion 2027-08-30 (estimated), first posted 2026-05-29, last updated 2026-05-29
Locations1 site in China

Related Papers Related Patents Related Grants Related Experts
All trials for Gastric Cancer (GC) All trials of Sodium propionate

-Summary

Eligible patients were randomized into two groups: the sodium propionate group and the control group. In the control group, patients received placebo combined with anti-PD-1 therapy plus chemotherapy without additional sodium propionate intervention. In the sodium propionate group, on the basis of anti-PD-1 therapy combined with chemotherapy, patients were additionally administered oral sodium propionate capsules at a dose of 500 mg (1 capsule) twice weekly, with a total intervention duration of 12 weeks. The primary and secondary outcome indicators will be collected for subsequent analysis.

Expand all sections  ·  Collapse all

+Detailed description

Eligible patients with unresectable gastric cancer were randomly assigned to either the sodium propionate group or the control group. In the control group, patients received placebo combined with anti-PD-1 therapy and chemotherapy, without additional sodium propionate intervention. In the sodium propionate group, on the basis of anti-PD-1 therapy combined with chemotherapy, patients were additionally given oral sodium propionate capsules at a dose of 500 mg per capsule, one capsule twice a week, for a total intervention period of 12 weeks. Relevant primary and secondary outcome measures will be collected for further analysis.

+Arms and interventions

ArmTypeInterventionsDescription
ControlNo interventionpatients received placebo combined with anti-PD-1 therapy and chemotherapy, without additional sodium propionate intervention.
Sodium propionateExperimentalDietary Supplement: Sodium propionateon the basis of anti-PD-1 therapy combined with chemotherapy, patients were additionally given oral sodium propionate capsules at a dose of 500 mg per capsule, one capsule twice a week, for a total intervention period of 12 weeks.
  • Sodium propionate (Dietary supplement), also known as Propionic acid: on the basis of anti-PD-1 therapy combined with chemotherapy, patients were additionally given oral sodium propionate capsules at a dose of 500 mg per capsule, one capsule twice a week, for a total intervention period of 12 weeks.

+Outcome measures

Primary outcomes

  • Response to treatment for gastric cancer [up to 12 weeks]: Tumor responses in patients with gastric cancer after corresponding treatment were evaluated in accordance with the Response Evaluation Criteria in Solid Tumors (RECIST 1.1).

Secondary outcomes

  • Tumor markers [up to 12 weeks]: Serum levels of CEA in ng/mL, CA19-9 in U/mL, CA72-4 in U/mL, AFP in ng/mL and CA125 in U/mL were routinely measured in patients on a monthly basis.
  • Patient survival [From date of randomization until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 12 months.]: Follow up on the survival status of patients

+Eligibility

Sex: All, ages: 18 Years to 80 Years

Inclusion Criteria:

* Subjects voluntarily participated in the trial and signed the informed consent form;
* Aged ≥ 18 years and < 80 years, regardless of gender;
* Stable vital signs;
* Patients with gastric adenocarcinoma confirmed by gastroscopic biopsy;
* Tumors judged as unresectable by attending physicians;
* Receiving anti-PD-1 therapy combined with chemotherapy as first-line treatment;
* No history of allergic diseases and non-allergic constitution;
* No history of drug abuse;
* Non-pregnant and non-lactating females (applicable to male subjects as well);
* No participation in any drug clinical trial (including investigational drugs of this trial) within 3 months prior to enrollment.

Exclusion Criteria:

* Failure to meet the inclusion criteria, or individuals deemed inappropriate for trial participation by investigators;
* Concurrent primary malignant tumors at other sites;
* Poor general condition, severe infection, respiratory insufficiency, or other conditions leading to inability to cooperate with the trial;
* Patients with mental disorders, consciousness disturbance, or poor treatment compliance;
* Suspected or confirmed history of drug abuse;
* Immunodeficiency, or long-term use of immunosuppressants and glucocorticoids;
* Pregnant or lactating women;
* Sponsors, investigators directly involved in this trial, and their immediate family members;
* Individuals unsuitable for enrollment for any reason as judged by the investigator.

+Locations (1)

FacilityCityCountryStatus
Xinying WangNanjing, JiangsuChina

+Publications

  • Duscha A, Gisevius B, Hirschberg S, Yissachar N, Stangl GI, Dawin E, Bader V, Haase S, Kaisler J, David C, Schneider R, Troisi R, Zent D, Hegelmaier T, Dokalis N, Gerstein S, Del Mare-Roumani S, Amidror S, Staszewski O, Poschmann G, Stuhler K, Hirche F, Balogh A, Kempa S, Trager P, Zaiss MM, Holm JB, Massa MG, Nielsen HB, Faissner A, Lukas C, Gatermann SG, Scholz M, Przuntek H, Prinz M, Forslund SK, Winklhofer KF, Muller DN, Linker RA, Gold R, Haghikia A. Propionic Acid Shapes the Multiple Sclerosis Disease Course by an Immunomodulatory Mechanism. Cell. 2020 Mar 19;180(6):1067-1080.e16. doi: 10.1016/j.cell.2020.02.035. Epub 2020 Mar 10. PMID 32160527
  • Yu L, Guo Q, Gu X, Wang Z, Li J, Wang X, Xu Z, Wang Y, Zhang Y, Zhang Y, Ding Y, Chen Z, Chen K, Ding Y. Impact of gut microbiome on radiotherapy and immunotherapy efficacy in microsatellite-stable colorectal cancer: role of propionic acid and B. fragilis. Br J Cancer. 2025 Oct;133(7):956-969. doi: 10.1038/s41416-025-03105-2. Epub 2025 Jul 26. PMID 40715695
  • Nomura M, Nagatomo R, Doi K, Shimizu J, Baba K, Saito T, Matsumoto S, Inoue K, Muto M. Association of Short-Chain Fatty Acids in the Gut Microbiome With Clinical Response to Treatment With Nivolumab or Pembrolizumab in Patients With Solid Cancer Tumors. JAMA Netw Open. 2020 Apr 1;3(4):e202895. doi: 10.1001/jamanetworkopen.2020.2895. PMID 32297948
  • Pham CH, Lee JE, Yu J, Lee SH, Yu KR, Hong J, Cho N, Kim S, Kang D, Lee S, Yoo HM. Anticancer Effects of Propionic Acid Inducing Cell Death in Cervical Cancer Cells. Molecules. 2021 Aug 16;26(16):4951. doi: 10.3390/molecules26164951. PMID 34443546
  • Eladwy RA, Fares M, Chang D, Alsherbiny MA, Li CG, Bhuyan DJ. Fuelling the Fight from the Gut: Short-Chain Fatty Acids and Dexamethasone Synergise to Suppress Gastric Cancer Cells. Cancers (Basel). 2025 Jul 28;17(15):2486. doi: 10.3390/cancers17152486. PMID 40805185