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
- PMID: 40211191
- PMCID: PMC11984019
- 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
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.
© 2025. The Author(s).
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.
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