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Hematopoietic Stem Cell Transplantation for the Treatment of Patients With Fanconi Anemia Lacking a Genotypically Identical Donor, Using a Chemotherapy Only Cytoreduction With Busulfan, Cyclophosphamide and Fludarabine

Phase 2
Completed
Conditions
Aplastic Anemia
Leukemia
Myelodysplastic Syndrome
Interventions
Registration Number
NCT00987480
Lead Sponsor
Memorial Sloan Kettering Cancer Center
Brief Summary

This is a genetic disease (transmitted through the parents' genes) called Fanconi Anemia. Because of that genetic disease, the bone marrow has changed and now has failed, or has given rise to a preleukemia called myelodysplastic syndrome (MDS) or leukemia (acute myelogenous leukemia or AML).

Without treatment these complications of Fanconia anemia (FA) are fatal. The only treatment that can cure these complications is an allogeneic transplant of stem cells, meaning, giving the patient bone marrow cells from a healthy donor that can produce normal blood cells that will replace the bone marrow that is sick.

What has been given for the treatment of FA in the past is to use a combination of low doses of radiation to the whole body (total body irradiation) and low doses of the chemotherapy drugs (cyclophosphamide and fludarabine) before the transplant. However, the use of radiation can, later on, increase the chances of getting a second cancer of the skin, head or the neck. These chances of a second cancer are higher than normal in patients with FA.

The purpose of this study is to find out if the doctors can do the same thing with the same chemotherapy drugs used in the past. However physicians will use another chemotherapy drug called busulfan instead of the radiation. The goal of this study is to get rid of the short term and long term risks of the radiation. The first new part of this treatment will be to replace drugs for radiation with chemotherapy drugs.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
45
Inclusion Criteria
  • Patients must have a diagnosis of Fanconi anemia (confirmed by mitomycin C or diepoxybutane [DEB] chromosomal breakage testing at an approved laboratory).

  • Hematologic Diagnosis and Status - Patients must have one of the following hematologic diagnoses:

    • Severe Aplastic Anemia (SAA) with bone marrow cellularity of <25%, or Severe Isolated Single lineage Cytopenia

AND at least one of the following features:

  • Platelet count <20 x 109/L or platelet transfusion dependence*

  • ANC <1000 x 109/L

  • Hgb <8 gm/dl or red cell transfusion dependence*

  • Myelodysplastic Syndrome (MDS) (Appendix 1: MDS Classification) - MDS at any stage, based on either one of the following classifications:

    • WHO Classification
    • Refractory anemia and transfusion dependence*
    • Any of other stages
    • IPSS Classification
    • Low risk (score 0) and transfusion dependence*
    • Any other risk groups Score > or = to 0.5
  • Acute Myelogenous Leukemia

    • Patients with acute leukemia are included in this trial in remission, refractory or relapsed disease.

    • Transfusion dependence will be defined as greater than ONE transfusion of platelets or red blood cells in the last year prior to evaluation on protocol.

      • Donors:
  • Donor choices will be determined by the investigators at each of the centers according to their own institutional criteria.

  • All patients evaluated at trial sites and eligible for this trial by virtue of disease and lack of an HLA-genotypically matched related donor will be captured in the database of this trial. Patients who will be enrolled on this protocol must have one of the following donor choices:

    • HLA-compatible Unrelated volunteer donors

    • Patients who do not have a related HLA-matched donor but have an unrelated donor who is either matched at all A, B, C and DRB1 (8/8) loci or who is mismatched at 1/8 loci (A, B, C or DRB1) (7/8) as tested by DNA analysis (high resolution), will be eligible for entry on this protocol.

    • HLA-mismatched Related donors

    • Patients who do not have a related or unrelated HLA-compatible donor must have a healthy family member who is at least HLA-haplotype identical to the recipient. First degree related donors must have a normal DEB test.

    • The donor must be healthy and willing and able to receive a 4-6 day course of G-CSF and undergo 1-3 daily leukaphereses.

    • Related and Unrelated donors must be medically evaluated and fulfill the criteria for collection of PBSCs as per institutional guidelines.

      • Patients:
  • Patients and donors may be of either gender or any ethnic background.

  • Patients must have a Karnofsky adult, or Lansky pediatric performance scale status > or = 70%.

  • At the time of referral for transplantation, patients must have no co-existing medical problems that would significantly increase the risk of the transplant procedure.

  • Patients must have adequate physical function measured by :

    • Cardiac: asymptomatic or if symptomatic then 1) LVEF at rest must be > or = to 50% and must improve with exercise or 2) Shortening Fraction > or = to 29%
    • Hepatic: < 5 x ULN SGOT and < 2.0 mg/dl total serum bilirubin.
    • Renal: serum creatinine < or = to 1.5 mg/dl or if serum creatinine is outside the normal range, then CrCl > 60-ml/min/1.73 m2
    • Pulmonary: asymptomatic or if symptomatic, DLCO > 50% of predicted (corrected for hemoglobin)
  • Each patient must be willing to participate as a research subject and must sign an informed consent form. Parent or legal guardians of patients who are minors will sign the informed consent form. Assents will be obtained as age appropriate.

  • Female patients and donors must not be pregnant or breastfeeding at the time of signing consent. Women must be willing to undergo a pregnancy test prior to transplant and avoid becoming pregnant while on study.

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Exclusion Criteria
  • Active CNS leukemic involvement
  • Female patients who are pregnant (positive serum or urine HCG) or breast-feeding. Women of childbearing age must avoid becoming pregnant while on study.
  • Active uncontrolled viral, bacterial or fungal infection
  • Patient seropositive for HIV-I/II; HTLV -I/II
Read More

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
chemotherapy-based cytoreductive regimen plus a CD34+ selectedCliniMACS deviceThis phase II trial is designed to investigate the safety and efficacy of a chemotherapy-based cytoreductive regimen plus a CD34+ selected T-cell depleted peripheral blood stem cell (PBSC) stem cell transplant for the treatment of patients with Fanconi anemia and severe hematologic disease.
chemotherapy-based cytoreductive regimen plus a CD34+ selectedBusulfan, fludarabine, & cyclophosphamide with immunosuppression with ATG and cyclosporine.This phase II trial is designed to investigate the safety and efficacy of a chemotherapy-based cytoreductive regimen plus a CD34+ selected T-cell depleted peripheral blood stem cell (PBSC) stem cell transplant for the treatment of patients with Fanconi anemia and severe hematologic disease.
Primary Outcome Measures
NameTimeMethod
Successful Neutrophil Engraftment2 years
The Incidence of Early Transplant Related Mortality2 years
The Incidence of Acute GvHD100 days
The Incidence of Chronic GvHD2 years
Secondary Outcome Measures
NameTimeMethod
Overall Survival at 3 Years3 years

Overall Survival is defined as time from date of transplant to event (death from any cause) or last follow-up.

Disease-free Survival at 3 Years3 years

Defined as time from date of transplant to relapse, graft rejection or graft failure, or death.

Primary non-engraftment is diagnosed when the participants fails to achieve an ANC \>/= 500/ul at any time in the first 28 days post-transplant.

For participants with MDS or AML, relapse will be analyzed as to type and genetic origin of the MDS/leukemic cells. These will be defined by an increasing number of blasts in the marrow over 5% by the presence of circulating peripheral blasts, or by the presence of blasts in any extramedullary site. Cytogenetic analysis of the marrow and/or peripheral blood will also be obtained for the diagnosis of relapse.

Trial Locations

Locations (6)

The Rockefeller University

🇺🇸

New York, New York, United States

Children's Hospital of Wisconsin

🇺🇸

Milwaukee, Wisconsin, United States

Memorial Sloan Kettering Cancer Center

🇺🇸

New York, New York, United States

Fred Hutchinson Cancer Research Center

🇺🇸

Seattle, Washington, United States

Cincinnati Children's Hospital

🇺🇸

Cincinnati, Ohio, United States

Children's Hospital Boston

🇺🇸

Boston, Massachusetts, United States

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