Early Use of Tacrolimus for Bone Marrow Transplant
What You Need to Know Before You Apply
What is the purpose of this trial?
This trial tests whether starting Tacrolimus earlier can reduce severe immune reactions after a bone marrow transplant. The goal is to make the transplant process safer and more effective for people with blood cancers requiring a stem cell transplant. Participants will receive a combination of three treatments: Cyclophosphamide, Mycophenolate mofetil, and Tacrolimus. Ideal candidates for the trial have a blood cancer that requires a stem cell transplant and a suitable family donor. As a Phase 2 trial, this research focuses on measuring the treatment's effectiveness in an initial, smaller group of people.
Do I need to stop my current medications for this trial?
The trial information does not specify whether you need to stop taking your current medications. It's best to discuss this with the trial coordinators or your doctor.
Is there any evidence suggesting that this trial's treatments are likely to be safe?
Research has shown that a combination of three drugs—tacrolimus, mycophenolate mofetil, and cyclophosphamide—in bone marrow transplants is generally safe. Specifically, using cyclophosphamide after a transplant has greatly reduced the risk of graft-versus-host disease (GVHD), where new immune cells attack the body.
One study linked this drug combination to a lower chance of cancer recurrence after the transplant, suggesting it might be both safe and effective. These studies have reported no major serious side effects, indicating that the treatment is usually well-tolerated.
This treatment is currently being tested in a Phase 2 trial, meaning it has already demonstrated some safety in earlier studies. However, further research is needed to confirm these results.12345Why are researchers excited about this trial's treatments?
Researchers are excited about using tacrolimus early in bone marrow transplants because it offers a unique approach to preventing graft-versus-host disease (GVHD), a common complication. Unlike standard treatments that often rely on drugs like methotrexate, tacrolimus works by suppressing the immune response more precisely, potentially reducing the risk of severe GVHD. Additionally, combining tacrolimus with mycophenolate mofetil and post-transplant cyclophosphamide might enhance its effectiveness and safety profile, offering a more tailored and potentially more successful treatment option for transplant patients.
What evidence suggests that this trial's treatments could be effective in reducing Cytokine Release Syndrome?
In this trial, participants will receive a combination of three drugs—tacrolimus, mycophenolate mofetil (MMF), and cyclophosphamide—to evaluate their effectiveness in reducing the risk of graft-versus-host disease (GVHD) after bone marrow transplants. Research has shown that using these drugs together significantly decreases the chances of GVHD and leads to better overall outcomes. Specifically, cyclophosphamide administered after the transplant has lowered the risk of cancer returning and improved survival rates. This combination is now considered more effective at preventing GVHD than the current standard treatment, with fewer side effects. Overall, evidence supports the effectiveness of this treatment in managing complications after stem cell transplants.23678
Who Is on the Research Team?
Melhem Solh, MD
Principal Investigator
The Blood and Marrow Transplant Group of Georgia
Are You a Good Fit for This Trial?
This trial is for individuals with blood disorders who are undergoing a specific bone marrow transplant called HLA-mismatched haploidentical transplantation. They should not have an organic affective disorder that could interfere with the study.Inclusion Criteria
Exclusion Criteria
Timeline for a Trial Participant
Screening
Participants are screened for eligibility to participate in the trial
Transplantation and Early Immunosuppression
Participants undergo hematopoietic stem cell transplantation followed by early immunosuppression with Tacrolimus, MMF, and Post-Transplant Cyclophosphamide
Follow-up
Participants are monitored for safety and effectiveness, including incidence of CRS and acute graft-versus-host disease
What Are the Treatments Tested in This Trial?
Interventions
- Cyclophosphamide
- Mycofenolate mofetil
- Tacrolimus
Find a Clinic Near You
Who Is Running the Clinical Trial?
Northside Hospital, Inc.
Lead Sponsor