Pilot Study Of Unrelated UCB Transplant for Non-Malignant Hematologic Conditions

Sponsor
Case Comprehensive Cancer Center (Other)
Overall Status
Completed
CT.gov ID
NCT00003336
Collaborator
National Cancer Institute (NCI) (NIH)
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Study Details

Study Description

Brief Summary

RATIONALE: Umbilical cord blood transplantation may allow doctors to give higher doses of chemotherapy or radiation therapy and kill more cancer cells.

PURPOSE: This phase II trial is studying how well umbilical cord blood transplantation works in treating patients with severe aplastic anemia, malignant thymoma, or myelodysplasia.

Condition or Disease Intervention/Treatment Phase
Phase 2

Detailed Description

OBJECTIVES:
  • Determine the rates of durable engraftment in patients with severe aplastic anemia, myelodysplastic syndrome, inborn errors of metabolism, or inherited hematopoietic disorders, refractory to medical management, who are undergoing high-dose chemoradiotherapy followed by unrelated cord blood (UCB) transplantation.

  • Evaluate the rate and quality of immunologic reconstitution in this patient population.

OUTLINE: Patients are stratified according to weight (under 45 kg vs over 45 kg).

Patients receive high-dose chemotherapy and/or radiotherapy as a conditioning regimen beginning 6-9 days before the umbilical cord blood transplant (UCBT). The regimen varies according to the underlying cause of the anemia, but could include busulfan, cyclophosphamide or melphalan, anti-thymocyte globulin or methylprednisolone, and/or radiation therapy. One day after the conditioning regimen is completed, patients receive the UCBT.

Patients are followed weekly for 3 months, at 6 months, then every 6 months for 2.5 years, then annually thereafter.

PROJECTED ACCRUAL: A total of 4-90 patients will be accrued for this study within 5 years.

Study Design

Study Type:
Interventional
Actual Enrollment :
6 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
A Pilot Study of Unrelated Umbilical Cord Blood Transplantation in Patients With Severe Aplastic Anemia, Inborn Errors in Metabolism, or Inherited Hematologic Stem Cell Disorders
Study Start Date :
Jan 1, 1998
Actual Primary Completion Date :
Dec 1, 2005
Actual Study Completion Date :
Feb 1, 2006

Outcome Measures

Primary Outcome Measures

  1. Event-free survival by disease assessment [at 100 days and at 6, 9, 12, 18, and 24 months]

Secondary Outcome Measures

  1. Umbilical cord blood donor engraftment by chimerism and complete blood count (CBC) at time of myeloid recovery. [100 days and at 6, 9, 12, 18, and 24 months]

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A to 55 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
DISEASE CHARACTERISTICS:
  • Histologically confirmed diagnosis of severe aplastic anemia based on bone marrow cellularity of less than 20%

  • Must meet at least two of the following criteria:

  • Granulocyte count less than 500/mm^3

  • Platelet count less than 20,000/mm^3

  • Reticulocyte count less than 50,000/mm^3

  • Following etiologies eligible:

  • Fanconi's anemia

  • Hypoplastic leukemia

  • Monosomy 7

  • Drug exposure (chloramphenicol, NSAIDS)

  • Viral exposure (EBV, hepatitis, parvovirus, HIV)

  • Nutritional deficiencies

  • Thymoma

  • Paroxysmal nocturnal hemoglobinuria

  • Amegakaryocytic thrombocytopenia OR

  • Histologically confirmed myelodysplastic syndrome (MDS) that is refractory to medical management or with cytogenic abnormalities predictive of transformation into acute leukemia, including 5q-, 7q-, monosomy 7, or trisomy 8

  • The following etiologies only are eligible:

  • Refractory anemia

  • Refractory anemia with ringed sideroblasts

  • De novo primary MDS

  • Therapy-related secondary MDS OR

  • Confirmed diagnosis of inherited hematopoietic disorder that is refractory to medical management

  • Following etiologies eligible:

  • Severe combined immunodeficiency

  • Familial erythrophagocytic lymphohistiocytosis

  • Wiskott-Aldrich syndrome

  • Kostmann's syndrome (infantile histiocytosis)

  • Chronic granulomatous disease

  • Leukocytic adhesion deficiency

  • Chediak-Higashi syndrome

  • Paroxysmal nocturnal hemoglobinuria

  • Fanconi's anemia

  • Dyskeratosis congenita

  • Diamond-Blackfan anemia

  • Amegakaryocytic thrombocytopenia

  • Osteopetrosis

  • Gaucher's disease

  • Lesch-Nyhan syndrome

  • Mucopolysaccharidoses

  • Lipodoses

  • Autologous or haploidentical related peripheral blood stem cells available as backup

  • Serologically matched umbilical cord blood unit available in the New York Blood Center's Placental Blood Project, or other acceptable umbilical cord blood registry

PATIENT CHARACTERISTICS:
Age:
  • 55 and under
Performance status:
  • Zubrod 0-1

  • Karnofsky 80-100%

Life expectancy:
  • At least 3 months
Hematopoietic:
  • See Disease Characteristics
Hepatic:
  • ALT/AST no greater than 4 times normal

  • Bilirubin no greater than 2.0 mg/dL

Renal:
  • Creatinine no greater than 2.0 mg/dL

  • Creatinine clearance at least 50 mL/min

Cardiovascular:
  • Normal cardiac function by echocardiogram or radionuclide scan

  • Shortening fraction or ejection fraction at least 80% normal for age

  • Non-Fanconi patients with acquired or congenital cardiomyopathy may receive melphalan as a substitute for cyclophosphamide

Pulmonary:
  • FVC and FEV_1 at least 60% of predicted for age

  • DLCO at least 60% of predicted in adult patients

Other:
  • No active concurrent malignancy

  • No active infection

  • Not pregnant or nursing

  • HIV negative

  • Must have an available serologic matched Umbilical Cord Blood Unit (UCBU) in the New York Blood Center's Placental Blood Project, or other acceptable Umbilical Cord Blood (UCB) registry

PRIOR CONCURRENT THERAPY:
Biologic therapy:
  • Not specified
Chemotherapy:
  • No concurrent cytotoxic chemotherapy
Endocrine therapy:
  • No concurrent immunosuppressive medications
Radiotherapy:
  • No concurrent radiotherapy
Surgery:
  • Not specified

Contacts and Locations

Locations

Site City State Country Postal Code
1 Ireland Cancer Center at University Hospitals Case Medical Center, Case Comprehensive Cancer Center Cleveland Ohio United States 44106-7284

Sponsors and Collaborators

  • Case Comprehensive Cancer Center
  • National Cancer Institute (NCI)

Investigators

  • Principal Investigator: Mary J. Laughlin, MD, Ireland Cancer Center at University Hospitals Case Medical Center, Case Comprehensive Cancer Center

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
, ,
ClinicalTrials.gov Identifier:
NCT00003336
Other Study ID Numbers:
  • CWRU5Y97
  • P30CA043703
  • CASE-CWRU-5Y97
  • NCI-G98-1431
  • CASE-5Y97
First Posted:
Jan 27, 2003
Last Update Posted:
Jun 11, 2010
Last Verified:
Jun 1, 2010

Study Results

No Results Posted as of Jun 11, 2010