Skip to main content
OpenTrials
Completed

NCT Number: NCT02248597

Donor Stem Cell Transplant Followed by Cyclophosphamide in Treating Patients With Hematological Diseases

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.

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year–69 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Comprehensive Cancer Center of Wake Forest University

Winston-Salem, North Carolina, 27157, United States

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Diagnosis of a hematological malignancy requiring an allogeneic stem cell transplant consistent with the standard of care
  • Remission of any acute hematologic malignancy or adequate disease control for chronic malignancies.
  • Ages 18-69 years old.
  • Available familial haploidentical (4 to 6 out of 8 HLA loci-matched) donor

Exclusion criteria

  • Significant organ dysfunction defined as: LV EF < 50% (evaluated by echocardiogram or MRI), DLCO or FEV1 < 65% predicted, AST/ALT > 2.5 x ULN, Bilirubin > 1.5 x ULN, Serum creatinine > 2mg/dL, dialysis, or prior renal transplant
  • HIV positive (Recipients who are positive for hepatitis B (HBV), hepatitis C (HCV) or human T-cell lymphotropic virus (HTLV-I/II) are not excluded from participation)
  • Positive pregnancy test for women of childbearing age.
  • Major anticipated illness or organ failure incompatible with survival form transplant.
  • Severe psychiatric illness or mental deficiency sufficiently severe as to make compliance with the transplant treatment unlikely and informed consent impossible.

Treatment and study plan

fludarabine phosphate

Drug

Given IV

Other names: 2-F-ara-AMP, Beneflur, Fludara

busulfan

Drug

Given IV

Other names: BSF, BU, Misulfan, Mitosan, Myeloleukon

Cyclophosphamide

Drug

Given IV

Other names: CPM, CTX, Cytoxan, Endoxan, Endoxana

allogeneic hematopoietic stem cell transplantation

Procedure

Undergo myeloablative or reduced intensity allogeneic stem cell transplant

Tacrolimus

Drug

Other names: FK 506, Prograf

Mycophenolate mofetil

Drug

Other names: Cellcept, MMF

Primary outcomes

  1. 12 Month Disease Free Survival Probability

    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.

Secondary outcomes

  1. Rate of Acute GvHD

    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.

  2. Overall Survival

    Time frame: At 12 months

    The survival function will be estimated and plotted using the method of Kaplan and Meier.

  3. Progression Free Survival

    Time frame: At 12 months

    Kaplan-Meier estimation of the percentage of patients who are alive without progressive disease at one year.

  4. Relapse-free Mortality

    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.

Sponsors and collaborators

Lead sponsor

Wake Forest University Health Sciences

Other

Collaborators

  • National Cancer Institute (NCI)

Registry information

Official study title

Haploidentical Stem Cell Transplant Using Post Transplant Cyclophosphamide for GvHD Prophylaxis: A Pilot Study

Important dates

Study start
2015
Primary completion
2022
Study completion
2023
First posted
Sep 25, 2014
Registry last updated
Oct 11, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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.

Published trials that share one or more normalized conditions with this study.