Randomized Phase 2 Study Testing Two Conditioning Regimen With a Single Prophylaxis of Graft-versus-host Disease by Cyclophosphamide and Methotrexate Post-transplant in Patients Eligible for Matched-donor Allograft Transplantation

Status: Recruiting
Location: See all (3) locations...
Intervention Type: Other, Drug, Radiation
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

Graft-versus-host disease (GVHD) is a major complication of allogeneic hematopoietic stem cell transplantation (allo-CSH). Recently, in the context of semi-identical (=haploidentical) HLA donors, but also of compatible HLA donors, the use of cyclophosphamide (CY) administered in high doses at early post-transplant (PT) (=PTCY) (Days +3 and +4 or +5) has shown excellent control of acute and chronic GVH, even enabling the discontinuation of other immunosuppressive drugs administered after allo-CSH (ciclosporin, mycophenolate mofetyl (MMF) or Cellcept). This step has already been taken in the context of allo-CSH with myeloablative conditioning (MAC), which is a minoritary conditioning in adults. However, in the context of allo-CSH with reduced-intensity conditioning (RIC), which predominates in adults, this strategy seems insufficient to prevent the risk of GVHD. The idea of reducing the use of immunosuppressants in the context of RIC/HLA-compatible transplants seems, however, still relevant, in order to reduce their adverse effects, improve patients' quality of life and enhance the reconstitution of the post-transplant immune system.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 70
Healthy Volunteers: f
View:

• Age: ≥ 18 and ≤ 70 years old

• Patient with hematologic malignancy

• Indication for HSC allograft with attenuated conditioning

• Pluripotent stem cell (PSC) engraftment

• Availability of a 10/10 familial or non-familial HLA compatible donor

• Consent to the protocol

• ECOG \<=2

• Woman of childbearing age with negative pregnancy test and on highly effective contraception during treatment and for a period of 12 months after stopping MTX and CY

• Man of childbearing age with highly effective contraception during treatment and for a period of 6 months after stopping MTX and CY and a period of 12 months after stopping MTX and CY if TBF conditioning regimen arm

• Negative Hepatitis B, C, HIV serologies

• Social security affiliation

Locations
Other Locations
France
CHU Angers
RECRUITING
Angers
CHU Brest
RECRUITING
Brest
CHU Nantes
RECRUITING
Nantes
Contact Information
Primary
Amandine LE BOURGEOIS, MD
amandine.lebourgeois@chu-nantes.fr
02 40 08 32 71
Time Frame
Start Date: 2024-07-18
Estimated Completion Date: 2028-07-18
Participants
Target number of participants: 82
Treatments
Experimental: (CLO)-BALTIMORE
BALTIMORE conditioning regime for LYMPHOID HEMOPATHY CLO-BALTIMORE conditioning regime for MYELOID HEMOPATHY
Active_comparator: TBF
Conditioning regimen for LYMPHOID AND MYELOID HEMOPATHY
Related Therapeutic Areas
Sponsors
Leads: Nantes University Hospital

This content was sourced from clinicaltrials.gov

Similar Clinical Trials