Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2025 Apr 10;25(1):656.
doi: 10.1186/s12885-025-14057-4.

A study protocol for a double-blinded, randomised, placebo-controlled trial on the use of encapsulated FMT for reducing the side effects of HSCT: the HSCT-BIOME study

Affiliations

A study protocol for a double-blinded, randomised, placebo-controlled trial on the use of encapsulated FMT for reducing the side effects of HSCT: the HSCT-BIOME study

Anna Li et al. BMC Cancer. .

Abstract

Background: The composition of the gut microbiota both prior to and after haematopoietic stem cell transplantation (HSCT) is increasingly implicated in the outcomes of HSCT, including infections, poor immune reconstitution and disease relapse. Faecal microbiota transplantation (FMT) offers a potential strategy of supporting the gut microbiota and improve HSCT outcomes. Although FMT has been investigated in HSCT recipients, it has largely been evaluated therapeutically for indications such as infection, or once immunocompetency is regained.

Methods: Peri-HSCT FMT (i.e. before and after HSCT) will be administered to eligible participants (adults undergoing autologous HSCT for a haematological malignancy) over two courses, with the first delivered immediately prior to conditioning and the second starting when ANC > 0.8. Following an open-label, safety run in (N = 5), peri-HSCT FMT will be evaluated for its efficacy in 51 participants, randomised 2:1 to FMT or placebo. The primary outcome is the proportion of participants who develop severe gastrointestinal toxicity defined by 3 consecutive days of severe diarrhoea (Bristol Stool Chart 6+), at a frequency of 4 + bowel movements/day within 3 weeks of HSCT. Safety is defined as the incidence of treatment-emergent adverse events (TE-AEs). Tolerability is defined as the incidence of TE-AEs and adherence to FMT.

Discussion: The HSCT-BIOME study is a multi-centre, double-blind, randomised placebo-controlled trial designed to determine the tolerability, safety and efficacy of orally-administered encapsulated FMT to promote the stability of the gastrointestinal microenvironment for HSCT recipients. Peri-HSCT delivered FMT is hypothesised to promote microbial composition both before and following HSCT. Thus, the study will determine if administration of FMT post-HSCT during the neutropenic phase will enhance efficacy.

Trial registration: ACTRN12624001104549. Date of registration: September 19, 2024 (prospectively registered).

Keywords: Autologous haematopoeitic stem cell transplantation; Capsule fecal microbiota transplantation; Peri-HSCT fecal microbiota transplantation.

PubMed Disclaimer

Conflict of interest statement

Declarations. Ethical approval and consent to participate: This study has been designed to comply with the Declaration of Helsinki, the ICH guidelines for Good Clinical Practice and NHMRC National Statement on Ethical Conduct in Research Involving Humans (2007, updated 2018). Ethics approval was obtained from the Human Research Ethics Committee of the Central Adelaide Local Health Network (CALHN), reference number: 2023/HRE00268. Written informed consent to participate in the study will be obtained from all participants. Consent for publication: Not applicable. Competing interests: Dr Samuel Costello and Dr Sarah Haylock-Jacobs are employees of BiomeBank and Dr Robert Bryant and Dr Samuel Costello are shareholders in BiomeBank.

Similar articles

References

    1. Touchefeu Y, Montassier E, Nieman K, et al. Systematic review: the role of the gut microbiota in chemotherapy- or radiation-induced Gastrointestinal mucositis - current evidence and potential clinical applications. Aliment Pharmacol Ther. 2014;40(5):409–21. 10.1111/apt.12878. [published Online First: 2014/07/22]. - PubMed
    1. van der Meij BS, de Graaf P, Wierdsma NJ, et al. Nutritional support in patients with GVHD of the digestive tract: state of the Art. Bone Marrow Transpl. 2013;48(4):474–82. 10.1038/bmt.2012.124. [published Online First: 2012/07/10]. - PubMed
    1. Ferrara JL, Levine JE, Reddy P, et al. Graft-versus-host disease. Lancet. 2009;373(9674):1550–61. 10.1016/s0140-6736(09)60237-3. [published Online First: 2009/03/14]. - PMC - PubMed
    1. Montassier E, Al-Ghalith GA, Ward T, et al. Pretreatment gut Microbiome predicts chemotherapy-related bloodstream infection. Genome Med. 2016;8(1):49. 10.1186/s13073-016-0301-4. [published Online First: 20160428]. - PMC - PubMed
    1. Harris B, Morjaria SM, Littmann ER, et al. Gut microbiota predict pulmonary infiltrates after allogeneic hematopoietic cell transplantation. Am J Respir Crit Care Med. 2016;194(4):450–63. 10.1164/rccm.201507-1491OC. - PMC - PubMed

Publication types

LinkOut - more resources