Myelodysplastic Syndrome Clinical Trial

Study of Allogeneic Bone Marrow Transplantation Following Cyclophosphamide and Radiotherapy in Patients With Myelodysplastic Syndrome and Acute Leukemia Related to Fanconi’s Anemia

Summary

OBJECTIVES:

I. Determine the effectiveness of moderate dose cyclophosphamide and radiotherapy in terms of improving survival and reducing the morbidity following allogeneic bone marrow transplantation in patients with myelodysplastic syndrome and acute leukemia related to Fanconi's anemia.

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Full Description

PROTOCOL OUTLINE:

Patients receive cyclophosphamide IV over 1-2 hours on day -6 through -3 and total body radiotherapy on day -1. Patients undergo allogeneic bone marrow transplantation on day 0.

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Eligibility Criteria

Diagnosis of Fanconi's anemia with the family history and typical phenotype including: Short stature Hypoplastic radii Skin pigmentation Renal anomalies Chromosomal fragility
Evidence of Fanconi's myelodysplastic syndrome Bone marrow dysplasia of all 3 marrow cell lines AND Clonal cytogenetic abnormalities demonstrable in marrow cells
First complete remission following therapy for Fanconi's acute leukemia allowed
Must have related histocompatible donor No evidence of excessive in vitro chromosome fragility typical of Fanconi's anemia Normal CBC and bone marrow

Study is for people with:

Myelodysplastic Syndrome

Study ID:

NCT00005892

Recruitment Status:

Completed

Sponsor:

Fairview University Medical Center

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There is 1 Location for this study

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Fairview University Medical Center
Minneapolis Minnesota, 55455, United States

How clear is this clinincal trial information?

Study is for people with:

Myelodysplastic Syndrome

Study ID:

NCT00005892

Recruitment Status:

Completed

Sponsor:


Fairview University Medical Center

How clear is this clinincal trial information?

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