Allogeneic Transplantation for Pediatric Leukemias With Unrelated Donors
Primary Purpose
Leukemia
Status
Unknown status
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
Busulfan
Fludarabine
Thymoglobulin
Total Body Irradiation
Sponsored by

About this trial
This is an interventional treatment trial for Leukemia focused on measuring Reduced Toxicity, Toxicity, Event Free Survival, Graft vs Host Disease
Eligibility Criteria
Inclusion Criteria:
- Ages 0-21
AML in one of the following stages:
- Having preceding myelodysplasia (MDS)
- High Risk cytogenetics
- Requiring > 2 cycles chemotherapy to obtain complete remission
- High allelic ratio FLT3/ITD+,
- Standard risk cytogenetics with positive MRD at end of Induction
- Second or greater CR
- First relapse with < 25% blasts in bone marrow
- With therapy-related AML whose prior malignancy has been in remission for at least 12 months
- ALL in one of the following stages:
High risk first remission, defined as:
- Ph+ ALL; or,
- 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,
- Hypodiploidy (< 44 chromosomes or DNA index < 0.81); or,
- End of induction M3 bone marrow; or,
- End of induction M2 marrow or MRD>1% with M2-3 marrow or MRD>1% at Day 42.
- High-risk infant ALL defined as age <6 months at diagnosis with MLL (11q23) translocation.
High risk second remission, defined as:
- Bone marrow relapse < 36 months from induction; or >36 mths if a matched sibling donor is available
- T-lineage relapse at any time; or,
- Very early isolated CNS relapse (<18 months from diagnosis); or,
- 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 first relapse must have < 25% blasts in bone marrow
- MDS at any stage; prior therapies allowed
- CML in chronic or accelerated phase; prior therapies allowed
Patient also must have the following organ requirements:
- Adequate renal function defined as serum creatinine <2x normal, or creatinine clearance > 40 ml/min/m^2 or 70 ml/min.
- Adequate liver function as defined by total bilirubin less than or equal to 2 times normal and AST and ALT less than or equal to 4 times normal.
- Adequate cardiac function as defined by: shortening fraction > 24% by echocardiogram, or ejection fraction > 30% by radionuclide angiogram.
- Adequate pulmonary function as defined by DLCO, FEV1/FVC > 60% by pulmonary function tests. For children who are uncooperative for PFTs and have no evidence of dyspnea at rest or exercise intolerance, pulse oximetry > 94% on room air is considered acceptable, with a normal chest xray.
- Adequate venous access; a double lumen central vascular access device or its equivalent and an additional PICC line will be required for all patients.
- Women of childbearing potential and sexually active males should use effective contraception while on study.
Exclusion Criteria:
- Inability to give informed consent or assent
- Inability to obtain a suitable donor
- Patient who is HIV-positive
- Patient who has active Hepatitis B
- Patient who is pregnant
- Patient who is otherwise considered unsuitable for transplant at the discretion of the principal investigator.
Sites / Locations
- Ann & Robert H. Lurie Children's Hospital of ChicagoRecruiting
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
A
Arm Description
All patients on this trial will receive a conditioning regimen of Busulfan, Fludarabine, Anti-Thymocyte Globulin and Total Body Irradiation (400 cGy)
Outcomes
Primary Outcome Measures
To evaluate the toxicity (as measures by 100 day survival) after hematopoietic stem cell transplant from an unrelated donor with a novel preparative regimen.
Secondary Outcome Measures
To evaluate the relapse-free and overall survival after hematopoietic stem cell transplant with Fludarabine/Busulfan/ATG/TBI preparative regimen for pediatric patients with leukemia.
To evaluate the incidence of acute and chronic graft-versus-host disease after hematopoietic stem cell transplant
Full Information
NCT ID
NCT00679536
First Posted
May 15, 2008
Last Updated
January 22, 2014
Sponsor
Ann & Robert H Lurie Children's Hospital of Chicago
1. Study Identification
Unique Protocol Identification Number
NCT00679536
Brief Title
Allogeneic Transplantation for Pediatric Leukemias With Unrelated Donors
Official Title
Allogeneic Transplantation for Pediatric Leukemias With Unrelated Donors Using Fludarabine, Busulfan, 400 cGy Total Body Irradiation, and Thymoglobulin
Study Type
Interventional
2. Study Status
Record Verification Date
January 2014
Overall Recruitment Status
Unknown status
Study Start Date
May 2008 (undefined)
Primary Completion Date
May 2015 (Anticipated)
Study Completion Date
May 2015 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Ann & Robert H Lurie Children's Hospital of Chicago
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The study proposes the use of Fludarabine, Busulfan, Anti Thymocyte Globulin Rabbit (ATG) and Total Body Irradiation as a preparative regimen before hematopoietic stem cell transplant from unrelated donor peripheral blood stem cells (PBSC). The hypothesis states that the 100 day mortality after this type of transplant will be significantly below the accepted standards, which is about 30% for unrelated donors.
Detailed Description
The primary objective of this study is to evaluate the toxicity (as measured as 100 day survival) after hematopoietic stem cell transplant from an unrelated donor with a novel preparative regimen of Fludarabine, Busulfan, Anti-Thymocyte Globulin, and Total Body Irradiation for pediatric patients with leukemia. The secondary objectives are to evaluate the relapse-free and overall survival after hematopoietic stem cell transplant as well as to evaluate the incidence of acute and chronic graft-versus-host disease after this preparative regimen.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Leukemia
Keywords
Reduced Toxicity, Toxicity, Event Free Survival, Graft vs Host Disease
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 1, Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
30 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
A
Arm Type
Experimental
Arm Description
All patients on this trial will receive a conditioning regimen of Busulfan, Fludarabine, Anti-Thymocyte Globulin and Total Body Irradiation (400 cGy)
Intervention Type
Drug
Intervention Name(s)
Busulfan
Other Intervention Name(s)
IV Busulfex
Intervention Description
Patient will receive a Test Dose of Busulfan on either Day -10 or Day -9. Patient will receive their Regimen Dose of Busulfan on Day -5 to Day -2. The regimen dose of Busulfan will be based off of the findings from their Test Dose.
Intervention Type
Drug
Intervention Name(s)
Fludarabine
Other Intervention Name(s)
Fludara
Intervention Description
Patient will receive Fludarabine from Day -6 to Day -2. The dose of Fludarabine will be 30 mg/m^2/day.
Intervention Type
Drug
Intervention Name(s)
Thymoglobulin
Intervention Description
The patient will also receive Thymoglobulin (rabbitATG) on Day -4 to Day -2. Each dose of rabbitATG will be 1.5 mg/kg/day.
Intervention Type
Radiation
Intervention Name(s)
Total Body Irradiation
Intervention Description
On Day -1 the patient will receive a total of 400 cGy of Total Body Irradiation.
Primary Outcome Measure Information:
Title
To evaluate the toxicity (as measures by 100 day survival) after hematopoietic stem cell transplant from an unrelated donor with a novel preparative regimen.
Time Frame
100 day mortality
Secondary Outcome Measure Information:
Title
To evaluate the relapse-free and overall survival after hematopoietic stem cell transplant with Fludarabine/Busulfan/ATG/TBI preparative regimen for pediatric patients with leukemia.
Time Frame
5 years
Title
To evaluate the incidence of acute and chronic graft-versus-host disease after hematopoietic stem cell transplant
Time Frame
5 years
10. Eligibility
Sex
All
Maximum Age & Unit of Time
21 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Ages 0-21
AML in one of the following stages:
Having preceding myelodysplasia (MDS)
High Risk cytogenetics
Requiring > 2 cycles chemotherapy to obtain complete remission
High allelic ratio FLT3/ITD+,
Standard risk cytogenetics with positive MRD at end of Induction
Second or greater CR
First relapse with < 25% blasts in bone marrow
With therapy-related AML whose prior malignancy has been in remission for at least 12 months
ALL in one of the following stages:
High risk first remission, defined as:
Ph+ ALL; or,
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,
Hypodiploidy (< 44 chromosomes or DNA index < 0.81); or,
End of induction M3 bone marrow; or,
End of induction M2 marrow or MRD>1% with M2-3 marrow or MRD>1% at Day 42.
High-risk infant ALL defined as age <6 months at diagnosis with MLL (11q23) translocation.
High risk second remission, defined as:
Bone marrow relapse < 36 months from induction; or >36 mths if a matched sibling donor is available
T-lineage relapse at any time; or,
Very early isolated CNS relapse (<18 months from diagnosis); or,
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 first relapse must have < 25% blasts in bone marrow
MDS at any stage; prior therapies allowed
CML in chronic or accelerated phase; prior therapies allowed
Patient also must have the following organ requirements:
Adequate renal function defined as serum creatinine <2x normal, or creatinine clearance > 40 ml/min/m^2 or 70 ml/min.
Adequate liver function as defined by total bilirubin less than or equal to 2 times normal and AST and ALT less than or equal to 4 times normal.
Adequate cardiac function as defined by: shortening fraction > 24% by echocardiogram, or ejection fraction > 30% by radionuclide angiogram.
Adequate pulmonary function as defined by DLCO, FEV1/FVC > 60% by pulmonary function tests. For children who are uncooperative for PFTs and have no evidence of dyspnea at rest or exercise intolerance, pulse oximetry > 94% on room air is considered acceptable, with a normal chest xray.
Adequate venous access; a double lumen central vascular access device or its equivalent and an additional PICC line will be required for all patients.
Women of childbearing potential and sexually active males should use effective contraception while on study.
Exclusion Criteria:
Inability to give informed consent or assent
Inability to obtain a suitable donor
Patient who is HIV-positive
Patient who has active Hepatitis B
Patient who is pregnant
Patient who is otherwise considered unsuitable for transplant at the discretion of the principal investigator.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Sonali Chaudhury, MD
Phone
312-227-4863
Email
schaudhury@luriechildrens.org
First Name & Middle Initial & Last Name or Official Title & Degree
Colleen E Rosen, BS, RN
Phone
312-227-4870
Email
crosen@luriechildrens.org
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sonali Chaudhury, MD
Organizational Affiliation
Ann & Robert H Lurie Children's Hospital of Chicago
Official's Role
Principal Investigator
Facility Information:
Facility Name
Ann & Robert H. Lurie Children's Hospital of Chicago
City
Chicago
State/Province
Illinois
ZIP/Postal Code
60611
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Sonali Chaudhury, MD
Phone
312-227-4863
Email
schaudhury@luriechildrens.org
First Name & Middle Initial & Last Name & Degree
Colleen E Rosen, BS, RN
Phone
312-227-4870
Email
crosen@luriechildrens.org
12. IPD Sharing Statement
Learn more about this trial
Allogeneic Transplantation for Pediatric Leukemias With Unrelated Donors
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