Third-party fecal microbiota transplantation for high-risk treatment-naïve acute GVHD of the lower GI tract

Author:

DeFilipp Zachariah1ORCID,Damania Ashish V.2,Kim Haesook T.3,Chang Chia-Chi2ORCID,El-Jawahri Areej1,McAfee Steven L.1,Bottoms AJ S.1,Toncheva Vesselina1,Smith Melissa M.1,Dolaher Maria1,Perry Lindsey1,White Meghan1,Diana Brittany1,Connolly Sheila1,Dey Bimalangshu R.1,Frigault Matthew J.1,Newcomb Richard A.1ORCID,O’Donnell Paul V.1,Spitzer Thomas R.1,Mansour Michael K.4ORCID,Weber Daniela5,Ajami Nadim J.2ORCID,Hohmann Elizabeth4,Jenq Robert R.26,Chen Yi-Bin1ORCID

Affiliation:

1. 1Hematopoietic Cell Transplant and Cellular Therapy Program, Massachusetts General Hospital, Boston, MA

2. 2Platform for Innovative Microbiome and Translational Research, Department of Genomic Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX

3. 3Department of Data Science, Dana-Farber Cancer Institute and Harvard T. H. Chan School of Public Health, Boston, MA

4. 4Division of Infectious Diseases, Massachusetts General Hospital, Boston, MA

5. 5Departments of Hematology and Oncology, Internal Medicine III, University of Regensburg, Regensburg, Germany

6. 6Department of Stem Cell Transplantation and Cellular Therapy, The University of Texas MD Anderson Cancer Center, Houston, TX

Abstract

Abstract Disruption of the intestinal microbiome is observed with acute graft-versus-host disease (GVHD) of the lower gastrointestinal (LGI) tract, and fecal microbiota transplantation (FMT) has successfully cured steroid-refractory cases. In this open-label, single-arm, pilot study, third-party, single-donor FMT was administered in combination with systemic corticosteroids to participants with high-risk acute LGI GVHD, with a focus on treatment-naïve cases. Participants were scheduled to receive 1 induction dose (15 capsules per day for 2 consecutive days), followed by 3 weekly maintenance doses, consisting of 15 capsules per dose. The primary end point of the study was feasibility, which would be achieved if ≥80% of participants able to swallow ≥40 of the 75 scheduled capsules. Ten participants (9 treatment-naïve; 1 steroid-refractory) were enrolled and treated. The study met the primary end point, with 9 of 10 participants completing all eligible doses. Organ-specific LGI complete response rate at day 28 was 70%. Initial clinical response was observed within 1 week for all responders, and clinical responses were durable without recurrent LGI GVHD in complete responders. Exploratory analyses suggest that alpha diversity increased after FMT. Although recipient microbiome composition never achieved a high degree of donor similarity, expansion of donor-derived species and increases in tryptophan metabolites and short-chain fatty acids were observed within the first 7 days after FMT. Investigation into the use of microbiome-targeted interventions earlier in the treatment paradigm for acute LGI GVHD is warranted. This trial was registered at www.ClinicalTrials.gov as #NCT04139577.

Publisher

American Society of Hematology

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1. Gut microbiota and immunosenescence in cancer;Seminars in Cancer Biology;2024-09

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