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Busulfan Monotherapy as Conditioning for Autologous Hematopoietic Progenitor Cell Transplantation

Primary Purpose

Acute Myeloid Leukemia (AML)

Status
Terminated
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
G-CSF
Leukapheresis
Busulfan
Stem cell reinfusion
Sponsored by
H. Lee Moffitt Cancer Center and Research Institute
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Acute Myeloid Leukemia (AML) focused on measuring Busulfan, Acute myeloid leukemia (AML), Hematopoietic Stem Cell Transplantation (HSCT), Dendritic cells, Bone marrow transplantation, PBSC mobilization, Autologous stem cells

Eligibility Criteria

56 Years - 74 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Patients must have had histologically confirmed diagnosis of AML, in 1st complete remission, by a pathologic review at the H. Lee Moffitt Cancer Center and Research Institute. Any induction/consolidation regimen is permitted. General Inclusion Criteria: Age 56-74 Able to give informed consent Hepatic and renal function: normal bilirubin, AST and ALT less than or equal to 2x normal limits, serum creatinine less than or equal to 1.5x normal Left ventricular ejection fraction (LVEF) must be in normal range FEV1 AND DLCO greater than or equal to 50% predicted (at planned time of transplantation) ECOG PS less than or equal to 2 (at planned time of transplantation) Disease Specific Inclusion Criteria: Adverse-risk karyotype (del 5/5q, 7/7q, 3q, greater than or equal to 3 abnormalities): Intermediate-risk karyotype [46 XY, +8, -Y, +6, or any other isolated (<3 total) non-random abnormality not included in the adverse-risk category or favorable-risk category below] AML arising from antecedent hematologic disorder (e.g. MDS) Secondary AML (t-AML) Exclusion Criteria: Acute Promyelocytic Leukemia(FAB M3) subtype Presence of (8;21) translocation or inversion 16/t(16;16) cytogenetic phenotype (i.e. favorable-risk AML) Eligible for and willing to undergo matched-sibling allogeneic transplantation Greater than 2 induction regimens required to achieve complete remission Duration of > 8 weeks between completion of induction chemotherapy and initiation of consolidation chemotherapy No prior malignancy is allowed, except for adequately treated basal cell (or squamous cell) skin cancer, in situ cervical cancer, or other cancer for which the patient has been disease-free for at least 5 years. Prior extensive radiation therapy (>25% of bone marrow reserve) Concomitant radiation therapy, chemotherapy, or immunotherapy Intrinsic impaired organ function (as stated above) Active infection Positive serum pregnancy test in women who have not yet reached menopause (no menstrual periods for >12 months or who have not undergone tubal ligation or complete hysterectomy. Women who are breast-feeding Positive HIV testing Presence of CNS leukemia Uncontrolled insulin-dependent diabetes mellitus or uncompensated major thyroid or adrenal gland dysfunction Physical or psychiatric conditions that in the estimation of the PI or his designee place the patient at high-risk of toxicity or non-compliance

Sites / Locations

  • H. Lee Moffitt Cancer Center & Research Institute

Arms of the Study

Arm 1

Arm Type

Other

Arm Label

Autologous Hematopoietic Progenitor Cell Transplantation

Arm Description

G-CSF Mobilization Leukepheresis Busulfan Stem Cell Reinfusion

Outcomes

Primary Outcome Measures

100-day Non-relapse Mortality
100-day non-relapse mortality is the number of participants who died before day 100 posttransplant from causes other than relapsed disease

Secondary Outcome Measures

Successful Autologous Stem Cell Collection
Number of subjects who were able to collect at least 2 million CD34+ cells/kg
Severe Regimen-related Toxicity
Number of participants with severe regimen-related toxicity within 2 years posttransplant. Severe regimen-related toxicity was defined as CTC (version 3)grade 4.
1 Year Event-free Survival
Number of participants alive and without disease relapse at 1 year posttransplant
1 Year Overall Survival
Number of participants alive at 1 year posttransplant

Full Information

First Posted
August 10, 2006
Last Updated
February 20, 2017
Sponsor
H. Lee Moffitt Cancer Center and Research Institute
Collaborators
ESP Pharma
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1. Study Identification

Unique Protocol Identification Number
NCT00363467
Brief Title
Busulfan Monotherapy as Conditioning for Autologous Hematopoietic Progenitor Cell Transplantation
Official Title
A Pilot Study of Intravenous, Targeted-Dose Busulfan Monotherapy as Conditioning for Autologous Hematopoietic Progenitor Cell Transplantation in High-Risk AML
Study Type
Interventional

2. Study Status

Record Verification Date
August 2011
Overall Recruitment Status
Terminated
Why Stopped
Low accrual
Study Start Date
May 2006 (undefined)
Primary Completion Date
May 2009 (Actual)
Study Completion Date
May 2009 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
H. Lee Moffitt Cancer Center and Research Institute
Collaborators
ESP Pharma

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
During the pre-transplantation phase (following completion of consolidation chemotherapy), patients will begin to receive G-CSF at 10 mcg/kg twice daily; leukapheresis will also be given until a target goal for recipient body weight is obtained, or up to a maximum of 5 days. Conditioning/Preparative therapy will follow PBSC collection for up to 30 days with Busulfan IV daily x 4 days; subsequent doses will be adjusted based on pharmacokinetic (plasma level)monitoring. Following 1 day of rest, stem cell reinfusion will begin with supportive care. During follow-up, patients will be monitored out to 730 days.
Detailed Description
Pre- Transplantation Phase - Twenty-four to 48 hours following completion of consolidation chemotherapy, patients will begin to receive G-CSF at 10 mcg/kg twice daily subcutaneously. Alternatively, patients may receive G-CSF alone (same dose) as mobilization therapy. Leukapheresis will begin day 4 of G-CSF administration and proceed according to institutional guidelines. Leukapheresis will continue until a target goal for recipient body weight is obtained, or up to a maximum of 5 days. A minimum recipient body weight is required to proceed to transplantation. Transplantation Phase a. Conditioning/Preparative therapy - up to 30 days following PBSC collection, patients will begin conditioning therapy with Busulfan IV daily x 4 days (transplantation days -5,-4,-3,-2). The day -5 and -4 dose will be 130mg/m2; subsequent doses will be adjusted based on pharmacokinetic monitoring. Busulfan plasma level monitoring, collected around the first dose of busulfan b. Stem cell reinfusion - following 1 day of rest, previously collected autologous peripheral blood stem cells will be infused. The administration of supportive measures (e.g. intravenous fluids, antihistamines) during stem cell reinfusion will be performed according to institutional guidelines. Supportive care Antibiotic prophylaxis- according to hospital/institutional guidelines, and at the discretion of the treating physician. Growth factor support Transfusion support Prophylaxis for busulfan-induced seizures During follow-up, patients will be seen at least weekly for the first month and there after periodically out to 730 days posttransplant. The following medical procedures will be done: Medical history and physical exam (including concurrent meds, vital signs, performance status and weight) Standard labs Bone marrow aspirate and biopsy

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Acute Myeloid Leukemia (AML)
Keywords
Busulfan, Acute myeloid leukemia (AML), Hematopoietic Stem Cell Transplantation (HSCT), Dendritic cells, Bone marrow transplantation, PBSC mobilization, Autologous stem cells

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
3 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Autologous Hematopoietic Progenitor Cell Transplantation
Arm Type
Other
Arm Description
G-CSF Mobilization Leukepheresis Busulfan Stem Cell Reinfusion
Intervention Type
Drug
Intervention Name(s)
G-CSF
Other Intervention Name(s)
filgrastim or NeupogenR
Intervention Description
Mobilization Option 1:Twenty-four to 48 hours following completion of consolidation chemotherapy, patients will begin to receive G-CSF at 10 mcg/kg twice daily subcutaneously. Mobilization Option 2: If patients have recovered hematologically from consolidation chemotherapy, they may receive G-CSF at 10 mcg/kg twice daily subcutaneously.
Intervention Type
Drug
Intervention Name(s)
Leukapheresis
Intervention Description
leukapheresis
Intervention Type
Drug
Intervention Name(s)
Busulfan
Other Intervention Name(s)
Busulfan (MyleranR, Busulfex™)
Intervention Description
Busulfan IV daily x 4 days (transplantation days -5,-4,-3,-2). The day -5 and -4 dose will be 130mg/m2
Intervention Type
Procedure
Intervention Name(s)
Stem cell reinfusion
Intervention Description
autologous stem cell transplant
Primary Outcome Measure Information:
Title
100-day Non-relapse Mortality
Description
100-day non-relapse mortality is the number of participants who died before day 100 posttransplant from causes other than relapsed disease
Time Frame
100 days post transplant
Secondary Outcome Measure Information:
Title
Successful Autologous Stem Cell Collection
Description
Number of subjects who were able to collect at least 2 million CD34+ cells/kg
Time Frame
At time of stem cell collection
Title
Severe Regimen-related Toxicity
Description
Number of participants with severe regimen-related toxicity within 2 years posttransplant. Severe regimen-related toxicity was defined as CTC (version 3)grade 4.
Time Frame
up to 100 days post translant
Title
1 Year Event-free Survival
Description
Number of participants alive and without disease relapse at 1 year posttransplant
Time Frame
1 year post transplant
Title
1 Year Overall Survival
Description
Number of participants alive at 1 year posttransplant
Time Frame
1 year post transplant

10. Eligibility

Sex
All
Minimum Age & Unit of Time
56 Years
Maximum Age & Unit of Time
74 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients must have had histologically confirmed diagnosis of AML, in 1st complete remission, by a pathologic review at the H. Lee Moffitt Cancer Center and Research Institute. Any induction/consolidation regimen is permitted. General Inclusion Criteria: Age 56-74 Able to give informed consent Hepatic and renal function: normal bilirubin, AST and ALT less than or equal to 2x normal limits, serum creatinine less than or equal to 1.5x normal Left ventricular ejection fraction (LVEF) must be in normal range FEV1 AND DLCO greater than or equal to 50% predicted (at planned time of transplantation) ECOG PS less than or equal to 2 (at planned time of transplantation) Disease Specific Inclusion Criteria: Adverse-risk karyotype (del 5/5q, 7/7q, 3q, greater than or equal to 3 abnormalities): Intermediate-risk karyotype [46 XY, +8, -Y, +6, or any other isolated (<3 total) non-random abnormality not included in the adverse-risk category or favorable-risk category below] AML arising from antecedent hematologic disorder (e.g. MDS) Secondary AML (t-AML) Exclusion Criteria: Acute Promyelocytic Leukemia(FAB M3) subtype Presence of (8;21) translocation or inversion 16/t(16;16) cytogenetic phenotype (i.e. favorable-risk AML) Eligible for and willing to undergo matched-sibling allogeneic transplantation Greater than 2 induction regimens required to achieve complete remission Duration of > 8 weeks between completion of induction chemotherapy and initiation of consolidation chemotherapy No prior malignancy is allowed, except for adequately treated basal cell (or squamous cell) skin cancer, in situ cervical cancer, or other cancer for which the patient has been disease-free for at least 5 years. Prior extensive radiation therapy (>25% of bone marrow reserve) Concomitant radiation therapy, chemotherapy, or immunotherapy Intrinsic impaired organ function (as stated above) Active infection Positive serum pregnancy test in women who have not yet reached menopause (no menstrual periods for >12 months or who have not undergone tubal ligation or complete hysterectomy. Women who are breast-feeding Positive HIV testing Presence of CNS leukemia Uncontrolled insulin-dependent diabetes mellitus or uncompensated major thyroid or adrenal gland dysfunction Physical or psychiatric conditions that in the estimation of the PI or his designee place the patient at high-risk of toxicity or non-compliance
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jeffrey E Lancet, MD
Organizational Affiliation
H. Lee Moffitt Cancer Center and Research Institute
Official's Role
Principal Investigator
Facility Information:
Facility Name
H. Lee Moffitt Cancer Center & Research Institute
City
Tampa
State/Province
Florida
ZIP/Postal Code
33612
Country
United States

12. IPD Sharing Statement

Links:
URL
http://www.moffitt.org
Description
Moffiitt Cancer Center Clinical Trials Website

Learn more about this trial

Busulfan Monotherapy as Conditioning for Autologous Hematopoietic Progenitor Cell Transplantation

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