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

This study has been completed.

Sponsored by: Fairview University Medical Center
Information provided by: Office of Rare Diseases (ORD)
ClinicalTrials.gov Identifier: NCT00005892
  Purpose

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.


Condition Intervention
Fanconi's Anemia
Myelodysplastic Syndromes
Leukemia, Nonlymphocytic, Acute
Leukemia, Lymphocytic, Acute
Drug: cyclophosphamide
Procedure: Allogeneic Bone Marrow Transplantation

MedlinePlus related topics:   Anemia    Bone Marrow Transplantation    Leukemia, Adult Acute    Leukemia, Adult Chronic    Leukemia, Childhood   

Drug Information available for:   Cyclophosphamide   

U.S. FDA Resources

Study Type:   Interventional
Study Design:   Treatment

Further study details as provided by Office of Rare Diseases (ORD):

Study Start Date:   March 2000

Detailed 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.

  Eligibility
Ages Eligible for Study:   up to 54 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No

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
  Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT00005892

Locations
United States, Minnesota
Fairview University Medical Center    
      Minneapolis, Minnesota, United States, 55455

Sponsors and Collaborators
Fairview University Medical Center

Investigators
Study Chair:     Daniel J. Weisdorf     Fairview University Medical Center    
  More Information


Study ID Numbers:   199/15100, UMN-MT-1985-01, UMN-MT-8501
First Received:   June 2, 2000
Last Updated:   June 23, 2005
ClinicalTrials.gov Identifier:   NCT00005892
Health Authority:   Unspecified

Keywords provided by Office of Rare Diseases (ORD):
Fanconi's anemia  
acute leukemia  
acute lymphocytic leukemia  
acute myeloid leukemia  
acute undifferentiated leukemia  
adult acute lymphoblastic leukemia  
adult acute lymphoblastic leukemia in remission  
adult acute myeloid leukemia  
adult acute myeloid leukemia in remission  
aplastic anemia  
childhood acute lymphoblastic leukemia  
childhood acute lymphoblastic leukemia in remission  
childhood acute myeloid leukemia
childhood acute myeloid leukemia in remission
de novo myelodysplastic syndrome
hematologic disorders
hematopoietic/lymphoid cancer
leukemia
myelodysplastic syndrome
oncologic disorders
previously treated myelodysplastic syndrome
rare disease
secondary myelodysplastic syndrome

Study placed in the following topic categories:
Leukemia, Lymphoid
Precancerous Conditions
Cyclophosphamide
Leukemia, Myeloid, Acute
Acute lymphoblastic leukemia, adult
Leukemia
Preleukemia
Fanconi's anemia
Anemia, Aplastic
Neoplasm Metastasis
Acute myeloid leukemia, adult
Acute myelocytic leukemia
Lymphoma
Myelodysplastic syndromes
Precursor Cell Lymphoblastic Leukemia-Lymphoma
Metabolic Diseases
Immunoproliferative Disorders
Hematologic Diseases
Fanconi Anemia
Myelodysplastic Syndromes
Myelodysplasia
Acute myelogenous leukemia
Rare Diseases
Anemia
Leukemia, Myeloid
Lymphatic Diseases
Genetic Diseases, Inborn
Metabolic disorder
Bone Marrow Diseases
Lymphoproliferative Disorders

Additional relevant MeSH terms:
Neoplasms by Histologic Type
Disease
Molecular Mechanisms of Pharmacological Action
Immune System Diseases
Immunologic Factors
Antineoplastic Agents
DNA Repair-Deficiency Disorders
Physiological Effects of Drugs
Immunosuppressive Agents
Pharmacologic Actions
Neoplasms
Anemia, Hypoplastic, Congenital
Pathologic Processes
Therapeutic Uses
Syndrome
Myeloablative Agonists
Antineoplastic Agents, Alkylating
Antirheumatic Agents
Alkylating Agents

ClinicalTrials.gov processed this record on December 03, 2008




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