Evidence map›Paper›PMID 39773995›Full record

ArticleBMJ open2024

Intestinal

Benjamin H Mullish, Andrew J Innes, Lauren A Roberts, Shian Anim-Burton, Lee Webber, Nicholas A Johnson, Rohma Ghani, Pakhshan Farshi, Anjum B Khan, Francesca Kinsella and 8 more

Abstract readClinical Trial Protocol
In one paragraph

Article in BMJ open, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Review
  2. Observational
  3. Review
  4. Review
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

18 authors.

Benjamin H MullishDivision of Digestive Diseases, Department of Metabolism, Digestion and Reproduction, Faculty of Medicine, Imperial College London, London, UK.ORCID http://orcid.org/0000-0001-6300-3100
Andrew J InnesCentre for Haematology, Department of immunology and inflammation, Faculty of Medicine, Imperial College London, London, UK.
Lauren A RobertsDivision of Digestive Diseases, Department of Metabolism, Digestion and Reproduction, Faculty of Medicine, Imperial College London, London, UK.
Shian Anim-BurtonCancer Research UK Imperial Centre, Clinical Trials Section, Department of Surgery and Cancer, Faculty of Medicine, Imperial College London, London, UK.
Lee WebberCancer Research UK Imperial Centre, Clinical Trials Section, Department of Surgery and Cancer, Faculty of Medicine, Imperial College London, London, UK.
Nicholas A JohnsonImperial Clinical Trials Unit, School of Public Health, Faculty of Medicine, Imperial College London, London, UK.ORCID http://orcid.org/0000-0002-3702-5530
Rohma GhaniDivision of Digestive Diseases, Department of Metabolism, Digestion and Reproduction, Faculty of Medicine, Imperial College London, London, UK.
Pakhshan FarshiDepartment of Haematology, Manchester Royal Infirmary, Manchester, UK.
Anjum B KhanDepartment of Haematology, Leeds Teaching Hospitals NHS Trust, Leeds, UK.
Francesca KinsellaDepartment of Haematology, University Hospitals Birmingham NHS Foundation Trust, Birmingham, UK.
Panagiotis KottaridisDepartment of Haematology, University College London Hospitals NHS Foundation Trust, London, UK.
Pramila KrishnamurthyDepartment of Haematology, King's College Hospital NHS Foundation Trust, London, UK.
Emma NicholsonDepartment of Haematology, The Royal Marsden Hospital, London, UK.
Renuka PalanicawandarCentre for Haematology, Department of immunology and inflammation, Faculty of Medicine, Imperial College London, London, UK.
Graham WheelerImperial Clinical Trials Unit, School of Public Health, Faculty of Medicine, Imperial College London, London, UK.
Frances DaviesDepartment of Infectious Diseases, Hammersmith Hospital, Imperial College Healthcare NHS Trust, London, UK.
Julian R MarchesiDivision of Digestive Diseases, Department of Metabolism, Digestion and Reproduction, Faculty of Medicine, Imperial College London, London, UK j.marchesi@imperial.ac.uk.
Jiří PavlůCentre for Haematology, Department of immunology and inflammation, Faculty of Medicine, Imperial College London, London, UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionLower diversity of the gut microbiome prior to allogeneic haematopoietic cell transplantation (HCT) correlates with reduced survival after the intervention. Most patients undergoing HCT for a haematological malignancy have previously received intensive chemotherapy, resulting in prolonged neutropenic episodes requiring broad-spectrum antibiotics; use of these has been linked to reduced microbiome diversity. Intestinal microbiota transplant (IMT) is a novel treatment approach that restores this diversity. We hypothesised that IMT performed prior to initiation of HCT conditioning restores microbiome diversity during the early stages of HCT, leading to decreased frequency of complications and improved outcomes of HCT. METHODS AND ANALYSIS: 50 adult patients receiving allogeneic HCT will be recruited into this phase IIa trial and randomised 1:1 to receive capsulised IMT or matched placebo shortly prior to initiation of HCT conditioning and followed for up to 12 months. The primary outcome will be to assess the increase in alpha diversity between pre-IMT and that measured at ~42 days after IMT administration (day +28 of HCT), comparing the difference between patients receiving IMT compared with placebo. Secondary outcomes will include tolerability, the dynamics of gut microbiome diversity metrics and taxonomy over all time points assessed, as well as clinical outcomes (including burden of invasive infections, days of fever, admission to intensive care, development of graft-vs-host disease and mortality). ETHICS AND DISSEMINATION: This study was approved by a UK Research Ethics Committee (REC reference: 23/NE/0105). Dissemination of results will be in concert with patient and public involvement group input and is expected to be primarily via abstract presentation at conferences and manuscripts in peer-reviewed journals. TRIAL REGISTRATION NUMBERS: NCT6355583; EudraCT: 2022-003617-10.

Indexed as

Gastrointestinal MicrobiomeHematopoietic Stem Cell TransplantationTransplantation, HomologousAdultClinical Trials, Phase II as TopicDouble-Blind MethodFecal Microbiota TransplantationFemaleHematologic NeoplasmsHumansMaleMulticenter Studies as TopicRandomized Controlled Trials as TopicTransplantation ConditioningBone marrow transplantationLeukaemiaMicrobiotaTransplant medicine

Identifiers

PMID39773995
PMCPMC11884074

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

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.