Fecal Microbiota Transplantation for the Prevention of Acute Graft Versus Host Disease in Adults Undergoing Allogeneic Hematopoietic Cell Transplantation

Fred Hutchinson Cancer Center (FHCC)

Status and phase: Active, not recruiting; Phase 2

Conditions: Acute Graft Versus Host Disease; Hematopoietic and Lymphatic System Neoplasm

Treatments: Drug: Placebo; Drug: Fecal Microbiota Transplantation Capsule

Study type: Interventional

Funder types: Other

Identifiers

NCT06026371

NCI-2023-05599 (Registry Identifier)

FHIRB0020155 (Other Identifier)

RG1123691 (Other Identifier)

Details and patient eligibility

About

This randomized placebo-controlled double-blind phase II trial tests whether fecal microorganism (microbiota) transplantation prevents severe acute graft versus host disease in adults undergoing allogeneic hematopoietic cell transplantation (HCT). Fecal microbiota transplantation involves receiving processed fecal material orally after allogeneic HCT in order to establish a healthy gut microbiota. Gut microbiota undergoes major alterations during allogeneic HCT because of antibiotic exposures, nutritional changes, and chemotherapy administration. Establishing a healthy gut microbiota via fecal transplantation may help prevent acute graft versus host disease in patients undergoing allogeneic HCT.

Full description

OUTLINE: The first 12 patients are assigned to group I, remaining patients are randomized to 1 of 2 groups.

GROUP I: Patients receive fecal microbiota capsules orally (PO) once daily (QD) for 7 days starting at the time of neutrophil engraftment and discontinuation of anti-bacterial antibiotics.

GROUP II: Patients receive placebo PO QD for 7 days starting at the time of neutrophil engraftment and discontinuation of anti-bacterial antibiotics.

After completion of study intervention, patients are followed up monthly until 12 months post-allogeneic HCT.

Enrollment: 138 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Age >= 18

• Signed informed consent

• Able to take oral medications

• Planned T-replete allogeneic hematopoietic cell transplantation for any indication. History of prior transplantation is allowed

• Planned GVHD prophylaxis using one of the following regimens:

  • Calcineurin inhibitor (tacrolimus or cyclosporine) plus methotrexate
  • Calcineurin inhibitor (tacrolimus or cyclosporine) plus mycophenolate mofetil (MMF)
  • Sirolimus plus cyclosporine plus MMF
  • Post-transplant cyclophosphamide plus calcineurin inhibitor (with or without MMF or sirolimus)

• One of the following HCT donor types:

  • Human leukocyte antigen (HLA)-matched sibling donor
  • 9/10 or 10/10 HLA-matched unrelated donor
  • HLA- haploidentical donor
  • Cord blood

• Willing to use at least 1 accepted method of contraception until day 180 after transplant and agree to not donate eggs/sperm for 180 days after

• Not pregnant or breast feeding

• ELIGIBILITY CRITERIA FOR RANDOMIZATION: Absolute neutrophil count (ANC) recovery to > 0.5 x 10^9/L from nadir, without ongoing growth factor support

• ELIGIBILITY CRITERIA FOR RANDOMIZATION: Discontinuation of all antibacterial antibiotics (except those used for Pneumocystis jiroveci prophylaxis) for 2 days

• ELIGIBILITY CRITERIA FOR RANDOMIZATION: Resolution of all acute toxicities (other than anemia and thrombocytopenia) to Common Terminology Criteria for Adverse Events (CTCAE) grade 2 or lower

• ELIGIBILITY CRITERIA FOR RANDOMIZATION: Ability to swallow capsules

• ELIGIBILITY CRITERIA FOR RANDOMIZATION: No grade II-IV acute GVHD

• ELIGIBILITY CRITERIA FOR RANDOMIZATION: No moderate to severe chronic GVHD

• ELIGIBILITY CRITERIA FOR RANDOMIZATION: No concurrent antibiotics to treat infections. Prophylactic antiviral and antifungal antibiotics used to prevent infections are allowed

Exclusion criteria

• Severe food allergy in the form of anaphylaxis or attributable symptoms requiring hospitalization
• History of chronic aspiration or conditions predisposing to aspiration (e.g. neuromuscular disorders)
• Receiving or planned to receive other experimental agents (including ex vivo T-cell depletion) to prevent GVHD. The use of other experimental agents is prohibited unless approved by the principal investigator (PI) of the other trial

Trial design

Primary purpose: Prevention

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Quadruple Blind

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138 participants in 2 patient groups, including a placebo group

Group I (fecal microbiota transplant)

Experimental group

Description:

Patients receive fecal microbiota capsules PO QD for 7 days

Treatment:

Drug: Fecal Microbiota Transplantation Capsule

Group II (Placebo)

Placebo Comparator group

Description:

Patients receive placebo PO QD for 7 days

Treatment:

Drug: Placebo