Feasibility of antibiotic-assisted fecal microbiota transplantation with immunotherapy for esophageal and gastric cancer

This phase I - II, single-institution clinical trial enrolls patients with unresectable advanced or recurrent esophageal or gastric cancer. Participants receive a 1-week course of oral antibiotics (amoxicillin, fosfomycin, and metronidazole) prior to transplantation. A single dose of donor-derived intestinal microbiota solution is administered via colonoscopy, followed by initiation of ICI-based therapy on the next day. The primary endpoint is the incidence of dose-limiting toxicity. Secondary endpoints include response rate, disease control rate, progression-free survival, overall survival, and adverse events. Comprehensive translational research is conducted using stool, blood, and tissue samples to characterize immune responses and identify biomarkers associated with A-FMT and ICI efficacy.<b>Trial registration:</b> jRCTs031240170.The study is ongoing, and patients are currently being enrolled. Enrollment started in June 2024. A total of 7 patients have been enrolled as of August 2025. This protocol is version 3.2.

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Publication Details

Journal
Future Oncology
Published
2025-12-17
DOI
https://doi.org/10.1080/14796694.2025.2599371
Primary Topic
Gut microbiota and health
Type
article
Field-Weighted Citation Impact
0.00
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article

Feasibility of antibiotic-assisted fecal microbiota transplantation with immunotherapy for esophageal and gastric cancer

Yuri Yoshinami, Dai Ishikawa, Hirokazu Shoji, Hiroshi Imazeki et al.
Future Oncology
Gut microbiota and health
article

Feasibility of antibiotic-assisted fecal microbiota transplantation with immunotherapy for esophageal and gastric cancer

Yuri Yoshinami, Dai Ishikawa, Hirokazu Shoji, Hiroshi Imazeki, Hikaru Watanabe, Atsuo Takashima, Shohei Koyama, Jun Terauchi, Hidekazu Hirano, Natsuko Okita, Hiroyuki Takamaru, Shotaro Yamaguchi, Kazuki Tanaka, Shun Yamamoto, Kana Ogawa, Ken Kato, Toshiharu Hirose
article en

Abstract

This phase I - II, single-institution clinical trial enrolls patients with unresectable advanced or recurrent esophageal or gastric cancer. Participants receive a 1-week course of oral antibiotics (amoxicillin, fosfomycin, and metronidazole) prior to transplantation. A single dose of donor-derived intestinal microbiota solution is administered via colonoscopy, followed by initiation of ICI-based therapy on the next day. The primary endpoint is the incidence of dose-limiting toxicity. Secondary endpoints include response rate, disease control rate, progression-free survival, overall survival, and adverse events. Comprehensive translational research is conducted using stool, blood, and tissue samples to characterize immune responses and identify biomarkers associated with A-FMT and ICI efficacy.<b>Trial registration:</b> jRCTs031240170.The study is ongoing, and patients are currently being enrolled. Enrollment started in June 2024. A total of 7 patients have been enrolled as of August 2025. This protocol is version 3.2.

Future OncologyVol. 21(30)
Juntendo University (JP), National Cancer Center (US), Ark Therapeutic (United States) (US), National Cancer Center Hospital East (JP), Juntendo University Hospital (JP)
Openalex Percentile: Top 63%
Gut microbiota and health
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