A Pilot Study of HSCT for Patients With High-risk Hemoglobinopathy Using a Nonmyeloablative Preparative Regimen

• ClinicalTrials.gov Identifier: NCT00427661
• Recruitment Status: Completed
• First Posted: January 29, 2007
• Results First Posted: August 18, 2016
• Last Update Posted: August 18, 2016
• Sponsor: University of Pittsburgh
• Information provided by (Responsible Party): Lakshmanan Krishnamurti, University of Pittsburgh

Tracking Information

• First Submitted Date: January 18, 2007
• First Posted Date: January 29, 2007
• Results First Submitted Date: February 19, 2016
• Results First Posted Date: August 18, 2016
• Last Update Posted Date: August 18, 2016
• Study Start Date: June 2002
• Actual Primary Completion Date: May 2014 (Final data collection date for primary outcome measure)

Current Primary Outcome Measures (submitted: July 8, 2016)

• Development of GVHD Within 1 Year of BMT [ Time Frame: 1 year ]
  GVHD is assessed by physical exam, bloodwork and biopsy.
• Engraftment at 1 Year Post BMT. [ Time Frame: 1 year ]
  Measurement of total PBMC chimerism

Original Primary Outcome Measures (submitted: January 26, 2007)

• GVHD at 100 days, 6 months and 1 year will be tabulated by grade.
• The incidence of ≥5% chimerism at 100 days, 6 months and 1 year will be estimated, and reported with 95% confidence bounds.
• The association between % donor chimerism of lymphocytes and erythroid precursors at day 30 to % donor chimerism in the bone marrow at 1 year will be assessed via the Spearman correlation coefficient.
• In addition, the Wilcoxon test will be used to assess association of the % chimerism on day 30 to successful transplantation, which is defined as ≥ 5% donor chimerism in the bone marrow at 1 year.

• Current Secondary Outcome Measures (submitted: July 8, 2016): Incidence of Grade 2-4 Acute GVHD. [ Time Frame: 100 days ]
• Original Secondary Outcome Measures: Not Provided
• Current Other Pre-specified Outcome Measures: Not Provided
• Original Other Pre-specified Outcome Measures: Not Provided

Descriptive Information

• Brief Title: A Pilot Study of HSCT for Patients With High-risk Hemoglobinopathy Using a Nonmyeloablative Preparative Regimen
• Official Title: A Pilot Study of Allogeneic Hematopoietic Stem Cell Transplantation for Patients With High Risk Hemoglobinopathy Using a Non-Myeloablative Preparative Regimen to Achieve Stable Mixed Chimerism

Brief Summary

Hypothesis 1: A novel nonmyeloablative condition regimen will be safe and efficacious in producing stable donor chimerism and cure of severe hemoglobinopathy.

Hypothesis 2: Stable donor chimerism will result in amelioration of cerebral vasculopathy, improved cerebral perfusion and neurocognitive function.

Specific Aim 1: Study the safety and efficacy of a novel non-toxic conditioning regimen for HSCT for patients with severe hemoglobinopathies and the kinetics of lineage specific chimerism after HSCT

We will test our hypothesis that a novel nonmyeloablative condition regimen will be safe and efficacious in producing stable donor chimerism and cure of severe hemoglobinopathy:

Specific Aim 2: Optimize the immunosuppressive regimen for HSCT patients through a thorough understanding of the pharmacokinetics of Busulfan (BU) and mycophenolate mofetil (MMF) in the patient population. This will involve:

1. Determine the pharmacokinetics of intravenously and orally administered MMF and intravenous BU in patients receiving HSCT.
2. Determine the relationship of Area under the curve (AUC) of BU and mean trough concentrations of mycophenolic acid (MPA) to engraftment and graft versus host disease (GVHD).
3. Determine the relationship of Area under the curve (AUC) and steady state concentration of BU to engraftment at day 30 and 1 year post HSCT.

Specific Aim 3: Study the effect of complete or partial donor chimerism on silent and overt cerebral vasculopathy, and neurocognitive functioning in patients with SCD undergoing HSCT. We will test our hypothesis that stable donor chimerism will result in improvement in cerebral vasculopathy and neurocognitive function. This will include.

1. Determine effect of transplantation silent and overt cerebral vasculopathy by comparison MRA and TCD 1 year after HSCT to pre-HSCT studies.
2. Determine effect on HSCT on neurocognitive function. Specific Aim 4: To determine the rate of T cell immune reconstitution in children with sickle cell disease following myeloablative compared to nonmyeloablative stem cell transplantation, using immunophenotyping assays, CDR3 spectratyping TREC analysis, and measurement of T cell specific donor engraftment.

• Detailed Description: Severe hemoglobinopathies such as sickle cell disease (SCD) and Thalassemia are associated with considerable morbidity, organ damage and premature mortality. Allogeneic hematopoietic stem cell transplantation (HSCT) is the only therapy that can cure a hemoglobinopathy. The applicability of HSCT for hemoglobinopathies is limited by the paucity of suitable donors, and risk of early regimen-related toxicity and the late effects. Reduction of the dose of myelotoxic drugs in preparative regimens prior to HSCT has the potential to increase the applicability of this curative option for patients with hemoglobinopathies. We hypothesize that a preparative regimen that maximizes host immunosuppression without myeloablation will be well tolerated and sufficient for engraftment of donor hematopoietic stem cells in patients with severe hemoglobinopathies. The long term objective of this research is to develop novel, less toxic approaches to HSCT for patients with severe hemoglobinopathies. Specific aims: 1. To evaluate the safety and efficacy of a novel nontoxic nonmyeloablative approach to hematopoietic stem cell transplantation for hemoglobinopathies. 2. To optimize the immunosuppressive regimen for HSCT patients through a thorough understanding of the pharmacokinetics of Busulfan (BU) and Mycophenolic acid (MPA) 3. To determine the effect of partial or complete donor chimerism on cerebral vasculopathy in patients with SCD. 4. To determine the rate of T cell immune reconstitution in children with sickle cell disease following myeloablative compared to nonmyeloablative stem cell transplantation, using immunophenotyping assays, CDR3 spectratyping TREC analysis, and measurement of T cell specific donor engraftment. Subjects meeting eligibility criteria in whom an human leukocyte antigen matched, partially mismatched related or unrelated donor of bone marrow or umbilical cord blood will receive a HSCT after a nonmyeloablative preparative regimen consisting of BU, Fludarabine (FLU), total lymphoid radiation and Anti-Thymocyte globulin followed by prophylaxis against graft versus host disease with cyclosporine A and MMF. Patients will be studied for survival, cure of hemoglobinopathy, absence of severe regimen related toxicity and graft versus host disease. The relationship of engraftment, survival and Graft versus host disease to kinetics of lineage specific donor chimerism and area under the curve for Mycophenolic acid and Busulfan will be studied.
• Study Type: Interventional
• Study Phase: Not Applicable
• Study Design: Allocation: N/A; Intervention Model: Single Group Assignment; Masking: None (Open Label); Primary Purpose: Treatment

Condition

• Sickle Cell Disease
• Thalassemia
• Hemoglobinopathies

Intervention

Other: Busulfan; Fludarabine; cyclosporine A and MMF

Hematopoietic stem cell transplantation from a matched sibling or unrelated donor following a reduced intensity conditioning regimen

Other Name: Busulfex, Fludara, Gengraf, CellCept

Study Arms

AHCT in High Risk SCD

Intervention: Busulfan; Fludarabine; cyclosporine A and MMF

Intervention: Other: Busulfan; Fludarabine; cyclosporine A and MMF

• Publications *: Not Provided

Recruitment Information

• Recruitment Status: Completed
• Actual Enrollment (submitted: July 8, 2016): 8
• Original Enrollment (submitted: January 26, 2007): 20
• Actual Study Completion Date: May 2014
• Actual Primary Completion Date: May 2014 (Final data collection date for primary outcome measure)

Eligibility Criteria

Inclusion Criteria:

• Patients with SCD 0-35 years of age with an HLA-identical or 1 HLA antigen mismatched bone marrow or up to 2 HLA antigen mismatched umbilical cord blood (UCB) donor with one or more of the following:

  • Stroke, CNS hemorrhage or a neurologic event lasting longer than 24 hours, or abnormal cerebral MRI or cerebral arteriogram or MRI angiographic study and impaired neuropsychological testing,
  • Acute chest syndrome with a history of recurrent hospitalizations or exchange transfusions,
  • Recurrent vaso-occlusive pain 3 or more episodes per year for 3 years or more years or recurrent priapism,
  • Impaired neuropsychological function and abnormal cerebral MRI scan,
  • Stage I or II sickle lung disease,
  • Sickle nephropathy (moderate or severe proteinuria or a glomerular filtration rate [GFR] 30-50% of the predicted normal value),
  • Bilateral proliferative retinopathy and major visual impairment in at least one eye,
  • Osteonecrosis of multiple joints with documented destructive changes,
  • Requirement for chronic transfusions but with RBC alloimmunization >2 antibodies during long term transfusion therapy.
  • Patients with transfusion dependent Thalassemia 0-35 years of age with an HLA-identical or 1 HLA antigen mismatched bone marrow or up to 2 HLA antigen mismatched UCB donor.

• Second Transplants

  • Patients with sickle cell disease or Thalassemia who have failed to engraft or have autologous recovery are eligible for this protocol.
  • Patients must meet above criteria.
  • If first transplant was a non-myeloablative regimen, the second transplant can occur at any time.
  • If the first transplant was a myeloablative regimen, then the second transplant must be > 6 months from the first transplant.

Exclusion Criteria:

• Patients with one or more of the following:

  • Karnofsky or Lansky performance score <70,
  • Acute hepatitis or evidence of moderate or severe portal fibrosis or cirrhosis on biopsy,
  • Stage III-IV lung disease,
  • GFR<30% predicted normal values.
  • Pregnant or lactating females.
• Active serious infection whereby patient has been on intravenous antibiotics for one week prior to study entry. Any patient with AIDS or ARC or HIV seropositivity. Any patient with invasive aspergillums infection within one year of study entry.
• Psychologically incapable of undergoing BMT with associated strict isolation or documented history of medical non-compliance.
• Patients not able to receive TLI due to prior radiation therapy.

Donor Inclusion Criteria

• Donor must be in good health based on review of systems and results of physical examination.
• Donor must have a normal hemoglobin, white count, platelet count and PTT.
• Female donors of childbearing potential must have a negative pregnancy test.

Donor Exclusion Criteria

• Donor has active infection (including HIV, hepatitis).
• Donor is a lactating female.

Donor Selection

In the case where more than one donor meets the eligibility criteria, donor selection will be guided by the following considerations:

• HLA A, B, DRB1 identical sibling donor is preferable to an unrelated donor
• Homozygous normal donor is preferable to heterozygote (carrier)
• ABO-compatible donor is preferable to ABO-incompatible donor
• Younger donor is preferable to older
• Cytomegalovirus seronegative donor is preferable to CMV seropositive donor, if the patient is CMV negative

Sex/Gender

• Sexes Eligible for Study: All

• Ages: 3 Years to 35 Years (Child, Adult)
• Accepts Healthy Volunteers: No
• Contacts: Contact information is only displayed when the study is recruiting subjects
• Listed Location Countries: United States

Administrative Information

• NCT Number: NCT00427661
• Other Study ID Numbers: IRB #0504048
• Has Data Monitoring Committee: Yes
• U.S. FDA-regulated Product: Not Provided
• IPD Sharing Statement: Not Provided
• Current Responsible Party: Lakshmanan Krishnamurti, University of Pittsburgh
• Original Responsible Party: Not Provided
• Current Study Sponsor: University of Pittsburgh
• Original Study Sponsor: Same as current
• Collaborators: Not Provided

Investigators

• Principal Investigator: Lakshmanan Krishnamurti, MD; Children's Hospital Medical Center, Cincinnati

• PRS Account: University of Pittsburgh
• Verification Date: July 2016