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Study Summary
No. ID02-407:.......Blood And Marrow Transplantation......Simrit Parmar......Stem Cell Transplantation and Cellular Therapy
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Study Summary Title
Study Summary
Number:
ID02-407
Study Title:Randomized trial of unmanipulated versus expanded cord blood
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Physician New Patient Referral
Name:Simrit ParmarPatients Call:800-392-1611 (in U.S.A.) 713-792-6161 (outside U.S.A.)
Dept:Stem Cell Transplantation and Cellular TherapyReferring MD
Call:
800-392-1611 (in U.S.A.) 713-792-6161 (outside U.S.A.)
Phone:713-792-8750
Contact us about clinical trials
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General Information
Disease Group:Blood And Marrow TransplantationSupported By:N/A
Phase of Study:Phase IIReturn
Visit:
First 2 - 3 months post discharge, patients will be seen initially on a daily
basis.
After this period of time, patients will be evaluated on a monthly basis during
6 months, every 3 months thereafter for a year, and every 6 months thereafter.
Treatment
Agents:
NoneHome Care:If needed, parenteral nutrition, antibiotics, IV fluids and antiemetics may be
given at home.
Treatment Loc:Only at MDACC
Estimated
Length of Stay
in Houston:
Initial phase of treatment: 30-50 days in the inpatient BMT unit.

Patients will be followed in the ATC bed unit after discharge. Readmissions may
be necessary.

Patients are expected to remain in Houston for 4 - 6 months.
Description/
Intervention:
The goal of this clinical research study is to learn if combining cord blood
units to make the cells "take" faster in recipients will help to improve the
results of cord blood transplants.
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Study Objectives / Outcomes
      Primary objective:

      In a prospective, phase II randomized study, to evaluate the transplantation of two unmanipulated cord blood units ("double cord blood" transplant) versus one unmanipulated and one expanded cord blood unit ("expanded cord blood transplant") in patients with hematologic malignancies following high-dose or nonmyeloablative therapy:

      a. To evaluate the rate, extent, and durability of hematopoietic reconstitution

      Secondary objectives:
a. To evaluate the rate and severity of graft versus host disease
b. To evaluate the rates of infectious complications
c. To evaluate the rates of disease-free and overall survival
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Study Status Information
Study Activation / Registration Date:
IRB Review and Approval Date:09/23/2002
Study Type:
Recruitment Status:Closed
Projected Accrual:N/A
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Enrollment Eligibility
If you do not meet the enrollment eligibility, there may be other treatment options for you. Please Contact the Referral Office for more information.

Inclusion Criteria:1) Disease-Specific Eligibility Requirements: Patients must have one of the following hematologic malignancies: 1. Acute Myelogenous Leukemia (AML), Myelodysplastic Syndrome (MDS) 2. Acute Lymphoblastic Leukemia (ALL) 3. Chronic Myelogenous Leukemia (CML) 4. Non-Hodgkin's Lymphoma (NHL) 5. Hodgkin's Disease (HD) 6. Chronic Lymphocytic Leukemia (CLL) 7. Chronic eosinophilic leukemia or Philadelphia chromosome negative CML.

2) Greater than 1 month old and <=60 years old for full myeloablative therapy.

3) Patients must have two CB units available which are matched with the patient at 4, 5, or 6/6 HLA class I (serological) and II (molecular) antigens. Each cord must contain at least 1E7 total nucleated cells/Kg recipient body weight in the pre-thawed fraction.

4) Patient must be willing to undergo bone marrow harvest or PBPC collection for use in case of engraftment failure. If the patient is unable or fails to successfully undergo the collection, a family member must be identified to donate hematopoietic stem cells for haploidentical transplant in case of engraftment failure. If autologous hematopoietic stem cells cannot be procured due to marrow contamination by malignancy, or due to harvest failure, and a haploidentical relative is not available or not willing to donate, two cord blood units can be used as the back-up graft.

5) Continuation to Criteria # 4: These units will be identified prior to enrollment in this study.

6) Regimen 1 (Myeloablative mel/thiotepa/fludarabine): 1.Patients with ALL, HD, NHL, AML, MDS, CML, CLL and Chronic eosinophilic leukemia who are candidates for full myeloablative therapy. 2.Performance score of at least 60% by Karnofsky (age >= 12 years), or Lansky Play-Performance Scale (age <12 years). 3.Age >=1 month <=60 years (high-dose).

7) Continuation to Criteria # 6: 4.Adequate major organ system function as demonstrated by:a. Left ventricular ejection function of at least 40%. b.Pulmonary function test demonstrating a diffusion capacity of at least 50%. predicted (high-dose). c.Creatinine < 1.6 mg/dL. d.SGPT/bilirubin <= to 2.0 x normal (high-dose).

8) Eligibility for Regimen 2 (Non-myeloablative Cy-Flu-TBI): 1. Patients with ALL, AML, MDS, CML, NHL, CLL, Chronic eosinophilic leukemia and HD who are not candidates for full myeloablative therapy. All patients who received a prior autologous transplant are eligible. 2. Performance score of at least 60% by Karnofsky or PS < 3 (ECOG) (age >= 12 years), or Lansky Play-Performance Scale (age <12 years) 3. Age >= 1 month <=80 years

9) Continuation to Criteria # 8: 4. Left ventricular ejection function of at least 30%; 5. Pulmonary function test demonstrating a diffusion capacity of at least 40% predicted; 6. Creatinine < 3.0 mg/dL; 7. SGPT <= to 4.0 x normal.

10) Regimen 3 (Myeloablative VP16-TBI): 1. Patients with ALL who are candidates for myeloablative therapy, and require a TBI-containing regimen. 2. Performance score of at least 60% by Karnofsky or PS < 2 (ECOG) (age >= 12 years), or Lansky Play-Performance Scale (age <12 years). 3. Age >= 1 month <=50 years. 4. Organ function requirements: a. Left ventricular ejection function of at least 50%. b. Pulmonary function test demonstrating a diffusion capacity of at least 50% predicted. c. Creatinine < 1.6 mg/dL. d. SGPT <= 2.0 x normal.

Exclusion Criteria:1) HIV positive.

2) Pregnancy.

3) Serious medical Condition.

4) Patients with signs & symptoms leading to positive lumbar puncture (malignant cells in the CSF) or to documented metastatic parenchymal disease are ineligible for this study.

5) Availability of appropriate, willing, HLA-matched related donor.

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Links
Registration Number: NCT00067002
Study Information on Clinical Trials Registry (clinicaltrials.gov)

Other Links:
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Results


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