Umbilical Cord Blood (UCB) Transplantation in Pediatric Patients With High Risk Leukemia and Myelodysplasia

NCT ID: NCT02007863

Last Updated: 2015-12-28

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 2 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2008-08-31
• Study Completion Date: 2014-06-30

Brief Summary

Unrelated Cord Blood (UCB) transplant in children is a viable stem cell transplant modality for patients with leukemia and myelodysplasia. UCB is now considered "Standard Of Care" in cases where a suitable living bone marrow donor is not available. The survival of UCB is similar to Matched Unrelated Marrow Transplant. This study is considered "Research" since UCB is not a licensed product and requires investigational new drug (IND). THERE ARE NO SPECIFIC RESEARCH QUESTIONS IN THIS PROTOCOL. This protocol merely provides UCB as a stem cell treatment modality to pediatric patients who may require it after a conditioning regimen that excludes Total Body Irradiation.

Detailed Description

The preparative regimen will consist of:

• Fludarabine: 25 mg/m2/day IV x 5 doses on Days -13, to -9
• Busulfan 1mg/kg IV every 6 hrs x 16 doses on Days -8 to -5
• Melphalan 45 mg/m2/day IV x 3 doses on days -4 to -2
• ATGAM 30mg/kg/day x 3 doses on Days -3 to -1
• Day 0 will be the day of the UCB Transplant
• The graft-versus-host-disease (GVHD) prophylaxis will be Cyclosporin A to maintain level 200-400 beginning on Day -3, through 200-400. Solumedrol at 1mg/kg/day on Day 1 until D+4, then solumedrol 2mg/kg/day until Day +19 or till absolute neutrophil count (ANC) reaches 500/mm2, then taper by 0.2 mg/kg/week.

Conditions

Leukemia; Myelodysplasia; Acute Lymphocytic Leukemia; Acute Myelogenous Leukemia

Keywords

Leukemia; Myelodysplasia; Acute lymphocytic leukemia; ALL; Acute myelogenous leukemia; AML; Pediatric

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Umbilical Cord Blood + Chemotherapy

Umbilical Cord Blood transfusion + Chemotherapy (Fludarabine + Busulfan + Melphalan)

Group Type: EXPERIMENTAL

Umbilical Cord Blood Transfusion

Intervention Type: PROCEDURE

Following the administration of the preparative therapy, all subjects will undergo UCB transplantation. Umbilical Cord Blood Transfusion will occur on Day 0

Fludarabine

Intervention Type: DRUG

Fludarabine 25 mg/m2/day will be administered over 30-60 minutes intravenous infusion on Days -13 through -9 for a total of 5 doses. Fludarabine will not be dose adjusted for body weight.

Busulfan

Intervention Type: DRUG

Busulfan IV (Busulfex) will be administered IV every 6 hours on days -8 through -5 for a total of 16 doses. Seizure prophylaxis prior to first dose of busulfan till Day -3 will be administered.

Melphalan

Intervention Type: DRUG

Melphalan 45 mg/m2/day will be administered over 60 minutes intravenous infusion on Days -4 through -2 for a total of 3 doses.

Interventions

Umbilical Cord Blood Transfusion

Following the administration of the preparative therapy, all subjects will undergo UCB transplantation. Umbilical Cord Blood Transfusion will occur on Day 0

Intervention Type: PROCEDURE

Fludarabine

Fludarabine 25 mg/m2/day will be administered over 30-60 minutes intravenous infusion on Days -13 through -9 for a total of 5 doses. Fludarabine will not be dose adjusted for body weight.

Intervention Type: DRUG

Busulfan

Busulfan IV (Busulfex) will be administered IV every 6 hours on days -8 through -5 for a total of 16 doses. Seizure prophylaxis prior to first dose of busulfan till Day -3 will be administered.

Intervention Type: DRUG

Melphalan

Melphalan 45 mg/m2/day will be administered over 60 minutes intravenous infusion on Days -4 through -2 for a total of 3 doses.

Intervention Type: DRUG

Other Intervention Names

UCB; Fludara; Busulfex; Alkeran

Eligibility Criteria

Inclusion Criteria

• Patients must be up to 21 years of age
• Patients cannot receive total body irradiation (TBI) because of:

• Young age - < 2 years at diagnosis of leukemia resulting in an age < 4 years at transplantation (due to risk of severe growth retardation and brain damage).
• Inability to tolerate TBI because of prior radiation or organ toxicity.
• Refractory/multiply relapsed leukemia, for which a traditional TBI/cyclophosphamide regimen would unlikely lead to a successful outcome.
• Patients must have a partially human leukocyte antigen (HLA)-matched UCB unit. Unit must be HLA-matched minimally at 4 of 6 HLA-A and B (at intermediate resolution by molecular typing) and DRB1 (at high resolution by molecular typing) loci with the patient. The unit must deliver a pre-cryopreserved nucleated cell dose of at least 2.5 x 10^7 per kilogram.
• Acute myelogenous leukemia (AML) at the following stages:

• High risk first complete remission (CR1), defined as:

• Having preceding myelodysplasia (MDS)
• High risk cytogenetics (High-risk cytogenetics: del (5q) -5, -7, abn (3q), t (6;9) complex karyotype (>= 5 abnormalities)
• Requiring > 2 cycles chemotherapy to obtain CR;
• Second or greater CR.
• First relapse with < 25% blasts in bone marrow.
• Patients with therapy-related AML whose prior malignancy has been in remission for at least 12 months.
• Acute lymphocytic leukemia (ALL) at the following stages:
• High risk first remission, defined as:

1. Ph+ ALL; or,

2. Myeloid/lymphoid leukemia (MLL) rearrangement with slow early response [defined as having M2 (5-25% blasts) or M3 (>25% blasts on bone marrow examination on Day 14 of induction therapy)]; or,

3. Hypodiploidy (< 44 chromosomes or DNA index < 0.81); or,

4. End of induction M3 bone marrow; or,

5. End of induction M2 with M2-3 at Day 42.

• High risk second remission, defined as:

1. Bone marrow relapse < 36 months from induction; or,

2. T-lineage relapse at any time; or,

3. Very early isolated central nervous system (CNS) relapse (6 months from diagnosis); or,

4. Slow reinduction (M2-3 at Day 28) after relapse at any time.

• Any third or subsequent CR.
• Biphenotypic or undifferentiated leukemia in any CR or if in 1st relapse must have < 25% blasts in bone marrow (BM).
• MDS at any stage.
• Chronic myelogenous leukemia (CML) in chronic or accelerated phase.
• All patients with evidence of CNS leukemia must be treated and be in CNS CR to be eligible for study.
• Patients ≥ 16 years old must have a Karnofsky score ≥ 70% and patients < 16 years old must have a Lansky score ≥ 70%.
• Signed informed consent.
• Patients with adequate physical function as measured by:

1. Cardiac: Left ventricular ejection fraction at rest must be > 40%, or shortening fraction > 26%

2. Hepatic: Bilirubin ≤ 2.5 mg/dL; and alanine transaminase (ALT), aspartate transaminase (AST) and Alkaline Phosphatase ≤ 5 x upper limit of normal (ULN)

3. Renal: Serum creatinine within normal range for age, or if serum creatinine outside normal range for age, then renal function (creatinine clearance or GFR) > 70 mL/min/1.73 m2.

4. Pulmonary: Diffusing capacity of the lungs for carbon monoxide (DLCO), Forced expiratory volume in 1 second (FEV1), Forced vital capacity (FVC) (diffusion capacity) > 50% of predicted (corrected for hemoglobin); if unable to perform pulmonary function tests, then O2 saturation > 92% of room air.

Exclusion Criteria

• Pregnant (B-positive HCG) or breastfeeding.
• Evidence of HIV infection or HIV positive serology.
• Current uncontrolled bacterial, viral or fungal infection (currently taking medication and progression of clinical symptoms).
• Autologous transplant < 6 months prior to enrollment.
• Prior autologous transplant for the disease for which the UCB transplant will be performed.
• Allogeneic hematopoietic stem cell transplant < 6 months prior to enrollment.
• Active malignancy other than the one for which the UCB transplant is being performed within 12 months of enrollment
• Active CNS leukemia.
• Requirement of supplemental oxygen.
• HLA-matched related donor able to donate.

• Maximum Eligible Age: 21 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

University of Miami

OTHER

Sponsor Role: lead

Responsible Party

Martin Andreansky

Associate Professor of Clinical

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Martin Andreasky, MD, PhD

Role: PRINCIPAL_INVESTIGATOR

University of Miami

Locations

Jackson Memorial Hospital

Miami, Florida, United States

University of Miami Sylvester Comprehensive Cancer Center

Miami, Florida, United States

Countries

United States

Other Identifiers

20080774

Identifier Type: -

Identifier Source: org_study_id