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  5. Intestinal Microbiota Transplant Prior to Allogeneic Stem Cell Transplant (MAST) trial: study protocol for a multi-centre, double-blinded, placebo-controlled, phase IIa trial
 
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Intestinal Microbiota Transplant Prior to Allogeneic Stem Cell Transplant (MAST) trial: study protocol for a multi-centre, double-blinded, placebo-controlled, phase IIa trial
File(s)
e093120.full.pdf (1.48 MB)
Published version
Author(s)
Mullish, Benjamin H
Innes, Andrew J
Roberts, Lauren A
Anim-Burton, Shian
Webber, Lee
more
Type
Journal Article
Abstract
Introduction Lower 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.
Date Issued
2024-12
Date Acceptance
2024-11-27
Citation
BMJ Open, 2024, 14 (12)
URI
http://hdl.handle.net/10044/1/116019
URL
https://bmjopen.bmj.com/content/14/12/e093120
DOI
https://www.dx.doi.org/10.1136/bmjopen-2024-093120
ISSN
2044-6055
Publisher
BMJ Publishing Group
Journal / Book Title
BMJ Open
Volume
14
Issue
12
Copyright Statement
© Author(s) (or their
employer(s)) 2024. Re-use
permitted under CC BY.
Published by BMJ Group.
License URL
https://creativecommons.org/licenses/by/4.0/
Identifier
https://bmjopen.bmj.com/content/14/12/e093120
Publication Status
Published
Article Number
e093120
Date Publish Online
2024-12-22
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