Comprehensive Cancer Center of Wake Forest University
Winston-Salem, North Carolina, 27157, United States
NCT Number: NCT02248597
This pilot clinical trial studies donor stem cell transplant followed by cyclophosphamide in treating patients with hematological diseases. Giving chemotherapy before a donor stem cell transplant helps stop the growth of cells in the bone marrow, including normal blood-forming cells (stem cells) and cancer cells. When the healthy stem cells from a donor are infused into the patient they may help the patient's bone marrow make stem cells, red blood cells, white blood cells, and platelets. Sometimes the transplanted cells from a donor can make an immune response against the body's normal cells (called graft-versus-host disease). Giving cyclophosphamide after the transplant may stop this from happening.
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Notify Me18 year–69 year
All sexes
Interventional
Phase 2
Winston-Salem, North Carolina, 27157, United States
PRIMARY OBJECTIVES:
I. To determine if haploidentical stem cell transplant using post-transplant cyclophosphamide results in 60% or better disease free survival (DFS) at 12 months at our institution.
SECONDARY OBJECTIVES:
I. To determine the rate of acute and chronic graft-versus-host disease (GvHD), non-relapse mortality, and relapse.
OUTLINE:
PREPARATIVE REGIMEN: Patients receive fludarabine phosphate intravenously (IV) once daily (QD) on days -6 to -2. Patients receiving myeloablative conditioning receive busulfan IV every 6 hours for 16 doses on days -7 to -4 and patients receiving reduced intensity conditioning receive busulfan IV every 6 hours for 8 doses on days -5 to -4. Patients also receive cyclophosphamide IV QD on days -3 and -2
TRANSPLANT: Patients undergo stem cell transplant on day 0.
GVHD PROPHYLAXIS: Patients receive cyclophosphamide QD on days 3 and 4, tacrolimus on days 5-180, and mycophenolate mofetil on days 5-35.
After completion of study treatment, patients are followed up periodically for 2 years.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Given IV
Other names: 2-F-ara-AMP, Beneflur, Fludara
Given IV
Other names: BSF, BU, Misulfan, Mitosan, Myeloleukon
Given IV
Other names: CPM, CTX, Cytoxan, Endoxan, Endoxana
Undergo myeloablative or reduced intensity allogeneic stem cell transplant
Other names: FK 506, Prograf
Other names: Cellcept, MMF
Time frame: At 12 months
The percentage of patients who experience death or disease relapse by one year will be calculated and a corresponding 95% confidence interval will be constructed using the normal approximation for binomial proportions. The survival function will be estimated and plotted using the method of Kaplan and Meier.
Time frame: 12 months
Kaplan-Meier estimation of the rate of acute GvHD in the study population at one year with a 95% confidence interval.
Time frame: At 12 months
The survival function will be estimated and plotted using the method of Kaplan and Meier.
Time frame: At 12 months
Kaplan-Meier estimation of the percentage of patients who are alive without progressive disease at one year.
Time frame: At 12 months
Non-relapse mortality will be defined as time from registration to death due to anything other than relapse of hematological malignancy. Patients who relapse will be treated as a competing risk.
Wake Forest University Health Sciences
Other
Haploidentical Stem Cell Transplant Using Post Transplant Cyclophosphamide for GvHD Prophylaxis: A Pilot Study
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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