Evidence map›Paper›PMID 29592876›Full record

Trial reportBlood advances2018

Third-party fecal microbiota transplantation following allo-HCT reconstitutes microbiome diversity.

Zachariah DeFilipp, Jonathan U Peled, Shuli Li, Jasmin Mahabamunuge, Zeina Dagher, Ann E Slingerland, Candice Del Rio, Betsy Valles, Maria E Kempner, Melissa Smith and 20 more

3 registry-linked trialsOpen access · goldAbstract readClinical Trial
In one paragraph

Trial report in Blood advances, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 3 registered trials, which are not on this map. Cited by 141 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
141citing papers in PubMed, 2 pooled it
17.2field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT02733744 early_phase1completednot on this map

A Pilot Study to Determine the Feasibility of Fecal MicrobiotaTransplantation (FMT) in Hematopoietic Stem Cell Transplantation (HSCT) Recipients

TypeinterventionalSponsorMassachusetts General HospitalRan2016 to 2017Enrolled18ConditionsBone Marrow TransplantationArmsFecal Microbiota Transplantation (FMT)
NCT06355583 phase2recruitingnot on this mapstarted 2024, after this paper: background citation

Intestinal Microbiota Transplant Prior to Allogeneic Stem Cell Transplant (MAST) Trial

TypeinterventionalSponsorImperial College LondonRan2024 to 2027Enrolled50ConditionsAcute Lymphoblastic Leukaemia, Acute Leukemia of Ambiguous Lineage, Chronic Myeloid Leukemia, Chronic Myelomonocytic LeukemiaArmsEBX-102, Placebo
NCT07172191 naenrolling by invitationnot on this mapstarted 2025, after this paper: background citation

Manipulation of the Enteral Microbiome by Fecal Microbiota Transplantation Among Adult Patients With Malignant Hematological Diseases

TypeinterventionalSponsorDel-Pest Central Hospital - National Institute of Hematology and Infectious DiseasesRan2025 to 2030Enrolled100ConditionsMalignant Hematologic NeoplasmArmsFecal Microbial Transplantation
3 · Its place in the literature

Who cites it

141 citing papers in PubMed, 2 syntheses or guidelines pooled it, 203 citations in OpenAlex.

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  3. Randomized Double-Blind Phase II Trial of Fecal Microbiota Transplantation Versus Placebo in Allogeneic Hematopoietic Cell Transplantation and AML.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2023
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81 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

30 authors at 9 institutions in 2 countries.

Zachariah DeFilippBlood and Marrow Transplant Program, Massachusetts General Hospital, Boston, MA.
Jonathan U PeledAdult Bone Marrow Transplantation Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.
Shuli LiDepartment of Biostatistics and Computational Biology, Dana-Farber Cancer Institute, Boston, MA.
Jasmin MahabamunugeDivision of Infectious Diseases, Massachusetts General Hospital, Boston, MA.
Zeina DagherDivision of Infectious Diseases, Massachusetts General Hospital, Boston, MA.
Ann E SlingerlandAdult Bone Marrow Transplantation Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.
Candice Del RioBlood and Marrow Transplant Program, Massachusetts General Hospital, Boston, MA.
Betsy VallesBlood and Marrow Transplant Program, Massachusetts General Hospital, Boston, MA.
Maria E KempnerBlood and Marrow Transplant Program, Massachusetts General Hospital, Boston, MA.
Melissa SmithBlood and Marrow Transplant Program, Massachusetts General Hospital, Boston, MA.
Jami BrownBlood and Marrow Transplant Program, Massachusetts General Hospital, Boston, MA.
Bimalangshu R DeyBlood and Marrow Transplant Program, Massachusetts General Hospital, Boston, MA.
Areej El-JawahriBlood and Marrow Transplant Program, Massachusetts General Hospital, Boston, MA.
Steven L McAfeeBlood and Marrow Transplant Program, Massachusetts General Hospital, Boston, MA.
Thomas R SpitzerBlood and Marrow Transplant Program, Massachusetts General Hospital, Boston, MA.
Karen K BallenDivision of Hematology/Oncology, University of Virginia School of Medicine, Charlottesville, VA.
Anthony D SungDivision of Hematologic Malignancies and Cellular Therapies and.
Tara E DaltonDivision of Hematologic Malignancies and Cellular Therapies and.
Julia A MessinaDivision of Infectious Diseases, Duke University School of Medicine, Durham, NC.
Katja DettmerInstitute of Functional Genomics, University of Regensburg, Regensburg, Germany.
Gerhard LiebischInstitute of Clinical Chemistry and Laboratory Medicine, University Hospital Regensburg, Regensburg, Germany.
Peter OefnerInstitute of Functional Genomics, University of Regensburg, Regensburg, Germany.
Ying TaurDepartment of Medicine, Weill Cornell Medical College, New York, NY.
Eric G PamerDepartment of Medicine, Weill Cornell Medical College, New York, NY.
Ernst HollerDepartment of Hematology and Oncology, Internal Medicine III, University Medical Center, Regensburg, Germany; and.
Michael K MansourDivision of Infectious Diseases, Massachusetts General Hospital, Boston, MA.
Marcel R M van den BrinkAdult Bone Marrow Transplantation Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.
Elizabeth HohmannDivision of Infectious Diseases, Massachusetts General Hospital, Boston, MA.
Robert R JenqDepartment of Genomic Medicine and.
Yi-Bin ChenBlood and Marrow Transplant Program, Massachusetts General Hospital, Boston, MA.
Massachusetts General Hospital · USMemorial Sloan Kettering Cancer Center · USCornell University · USUniversity Hospital Regensburg · DEUniversity of Regensburg · DEDana-Farber Cancer Institute · USDuke University · USThe University of Texas MD Anderson Cancer Center · USUniversity of Virginia · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
T LYMPHOCYTE SUBSET FUNCTION POST-TRANSPLANTATIONP01CA023766 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI DEVLIN, SEAN · 1985 to 2023
$59.0M
Resource Core 3 - Metabolomics CoreP30AG028716 · NIA · DUKE UNIVERSITY · PI Virginia B Kraus · 2006 to 2026
$24.6M
Systems Biology of Microbiome-mediated Resilience to Antibiotic-resistant PathogensU01AI124275 · NIAID · SLOAN-KETTERING INST CAN RESEARCH · PI PAMER, ERIC G., XAVIER, JOAO · 2016 to 2020
$8.9M
Protecting colonic mucus to mitigate acute intestinal graft-versus-host diseaseR01HL124112 · NHLBI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI JENQ, ROBERT · 2015 to 2024
$6.8M
The role of autophagy gene Atg16L1 in allogeneic hematopoietic stem cell transplantation - Resubmission - 1R01HL123340 · NHLBI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI CADWELL, KEN HASHIGIWA, VAN DEN BRINK, MARCEL R M · 2015 to 2022
$5.2M
Duke CTSA (Composite)KL2TR001115 · NCATS · DUKE UNIVERSITY · PI BOULWARE, LEIGH E, KRAFT, MONICA · 2013 to 2017
$5.1M
Transplant Infectious Diseases Interdisciplinary Research Training Grant (TIDIRTGT32AI100851 · NIAID · DUKE UNIVERSITY · PI ALEXANDER, BARBARA D · 2013 to 2022
$1.8M
Subcellular Mechanisms for Fungal Phagosome Maturation in MacrophagesK08AI110655 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI MANSOUR, MICHAEL K · 2014 to 2017
$759k
Data commons for 'omic, microscopy and analysis core facilitiesS10OD018164 · OD · DUKE UNIVERSITY · PI WRAY, GREGORY A. · 2014 to 2014
$598k
NCATS NIH HHS KL2 TR001115NCI NIH HHS P01 CA023766NCI NIH HHS P30 CA008748NHLBI NIH HHS R01 HL123340NHLBI NIH HHS R01 HL124112NIAID NIH HHS K08 AI110655NIAID NIH HHS T32 AI100851NIAID NIH HHS U01 AI124275NIA NIH HHS P30 AG028716NIH HHS S10 OD018164
6 · The paper itself

Abstract

We hypothesized that third-party fecal microbiota transplantation (FMT) may restore intestinal microbiome diversity after allogeneic hematopoietic cell transplantation (allo-HCT). In this open-label single-group pilot study, 18 subjects were enrolled before allo-HCT and planned to receive third-party FMT capsules. FMT capsules were administered no later than 4 weeks after neutrophil engraftment, and antibiotics were not allowed within 48 hours before FMT. Five patients did not receive FMT because of the development of early acute gastrointestinal (GI) graft-versus-host disease (GVHD) before FMT (n = 3), persistent HCT-associated GI toxicity (n = 1), or patient decision (n = 1). Thirteen patients received FMT at a median of 27 days (range, 19-45 days) after HCT. Participants were able to swallow and tolerate all FMT capsules, meeting the primary study endpoint of feasibility. FMT was tolerated well, with 1 treatment-related significant adverse event (abdominal pain). Two patients subsequently developed acute GI GVHD, with 1 patient also having concurrent bacteremia. No additional cases of bacteremia occurred. Median follow-up for survivors is 15 months (range, 13-20 months). The Kaplan-Meier estimates for 12-month overall survival and progression-free survival after FMT were 85% (95% confidence interval, 51%-96%) and 85% (95% confidence interval, 51%-96%), respectively. There was 1 nonrelapse death resulting from acute GI GVHD (12-month nonrelapse mortality, 8%; 95% confidence interval, 0%-30%). Analysis of stool composition and urine 3-indoxyl sulfate concentration indicated improvement in intestinal microbiome diversity after FMT that was associated with expansion of stool-donor taxa. These results indicate that empiric third-party FMT after allo-HCT appears to be feasible, safe, and associated with expansion of recipient microbiome diversity. This trial was registered at www.clinicaltrials.gov as #NCT02733744.

Indexed as

AdultAgedAllograftsBacteremiaFecal Microbiota TransplantationFemaleGastrointestinal TractGraft vs Host DiseaseHematopoietic Stem Cell TransplantationHumansMaleMicrobiotaMiddle AgedPilot ProjectsSurvival Analysis

Identifiers

PMID29592876
PMCPMC5894265
OpenAlexW2795193038

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.