Your browser doesn't support javascript.
loading
Third-party fecal microbiota transplantation for high-risk treatment-naïve acute GVHD of the lower GI tract.
DeFilipp, Zachariah; Damania, Ashish V; Kim, Haesook T; Chang, Chia-Chi; El-Jawahri, Areej; McAfee, Steven L; Bottoms, Aj S; Toncheva, Vesselina; Smith, Melissa M; Dolaher, Maria; Perry, Lindsey; White, Meghan; Diana, Brittany; Connolly, Sheila; Dey, Bimalangshu R; Frigault, Matthew J; Newcomb, Richard A; O'Donnell, Paul V; Spitzer, Thomas R; Mansour, Michael K; Weber, Daniela; Ajami, Nadim J; Hohmann, Elizabeth; Jenq, Robert R; Chen, Yi-Bin.
Afiliación
  • DeFilipp Z; Hematopoietic Cell Transplant and Cellular Therapy Program, Massachusetts General Hospital, Boston, MA.
  • Damania AV; Platform for Innovative Microbiome and Translational Research, Department of Genomic Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX.
  • Kim HT; Department of Data Science, Dana-Farber Cancer Institute and Harvard T. H. Chan School of Public Health, Boston, MA.
  • Chang CC; Platform for Innovative Microbiome and Translational Research, Department of Genomic Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX.
  • El-Jawahri A; Hematopoietic Cell Transplant and Cellular Therapy Program, Massachusetts General Hospital, Boston, MA.
  • McAfee SL; Hematopoietic Cell Transplant and Cellular Therapy Program, Massachusetts General Hospital, Boston, MA.
  • Bottoms AS; Hematopoietic Cell Transplant and Cellular Therapy Program, Massachusetts General Hospital, Boston, MA.
  • Toncheva V; Hematopoietic Cell Transplant and Cellular Therapy Program, Massachusetts General Hospital, Boston, MA.
  • Smith MM; Hematopoietic Cell Transplant and Cellular Therapy Program, Massachusetts General Hospital, Boston, MA.
  • Dolaher M; Hematopoietic Cell Transplant and Cellular Therapy Program, Massachusetts General Hospital, Boston, MA.
  • Perry L; Hematopoietic Cell Transplant and Cellular Therapy Program, Massachusetts General Hospital, Boston, MA.
  • White M; Hematopoietic Cell Transplant and Cellular Therapy Program, Massachusetts General Hospital, Boston, MA.
  • Diana B; Hematopoietic Cell Transplant and Cellular Therapy Program, Massachusetts General Hospital, Boston, MA.
  • Connolly S; Hematopoietic Cell Transplant and Cellular Therapy Program, Massachusetts General Hospital, Boston, MA.
  • Dey BR; Hematopoietic Cell Transplant and Cellular Therapy Program, Massachusetts General Hospital, Boston, MA.
  • Frigault MJ; Hematopoietic Cell Transplant and Cellular Therapy Program, Massachusetts General Hospital, Boston, MA.
  • Newcomb RA; Hematopoietic Cell Transplant and Cellular Therapy Program, Massachusetts General Hospital, Boston, MA.
  • O'Donnell PV; Hematopoietic Cell Transplant and Cellular Therapy Program, Massachusetts General Hospital, Boston, MA.
  • Spitzer TR; Hematopoietic Cell Transplant and Cellular Therapy Program, Massachusetts General Hospital, Boston, MA.
  • Mansour MK; Division of Infectious Diseases, Massachusetts General Hospital, Boston, MA.
  • Weber D; Departments of Hematology and Oncology, Internal Medicine III, University of Regensburg, Regensburg, Germany.
  • Ajami NJ; Platform for Innovative Microbiome and Translational Research, Department of Genomic Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX.
  • Hohmann E; Division of Infectious Diseases, Massachusetts General Hospital, Boston, MA.
  • Jenq RR; Platform for Innovative Microbiome and Translational Research, Department of Genomic Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX.
  • Chen YB; Department of Stem Cell Transplantation and Cellular Therapy, The University of Texas MD Anderson Cancer Center, Houston, TX.
Blood Adv ; 8(9): 2074-2084, 2024 May 14.
Article en En | MEDLINE | ID: mdl-38471063
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.
Asunto(s)

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Trasplante de Microbiota Fecal / Enfermedad Injerto contra Huésped Límite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Blood Adv Año: 2024 Tipo del documento: Article

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Trasplante de Microbiota Fecal / Enfermedad Injerto contra Huésped Límite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Blood Adv Año: 2024 Tipo del documento: Article