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Clofarabine, Cytarabine, and Thymoglobulin for Allogeneic Transplantation

Primary Purpose

Myelodysplastic Syndromes, Acute Myeloid Leukemia

Status
Terminated
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Clofarabine
Cytarabine
Thymoglobulin
Stem cell infusion
Sponsored by
Washington University School of Medicine
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Myelodysplastic Syndromes focused on measuring Conditioning regimens, Stem Cell Transplantation, Hematopoietic Stem Cell Transplantation, Allogeneic Stem Cell Transplantation, Nonmyeloablative conditioning, Clofarabine, Cytarabine, Anti-thymocyte globulin

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria (Patient):

  1. Myelodysplastic Syndrome (MDS), as defined by the World Health Organization criteria, OR Chronic Myelomonocytic Leukemia (CMML) as defined by the French American British classification OR Acute Myeloid Leukemia (AML) in complete remission [excluding FAB-M3] diagnosed by standard criteria and meet the criteria below:

    1. Patients may be in any CR
    2. No more than 2 cycles of consolidation. Any consolidation regimen may be used.
    3. No more than 6 months from documented CR to transplant.
  2. Age 18 years or older.
  3. ECOG performance status <=2
  4. Identification of suitable donor
  5. DLCO >=40% with no symptomatic pulmonary disease
  6. LVEF by MUGA >= 30%
  7. Serum creatinine <=1.0 mg/dL; if serum creatinine >1.0 mg/dL, then the estimated glomerular filtration rate (GFR) must be >60 mL/min/1.73 m2 as calculated by the Modification of Diet in Renal Disease equation where Predicted GFR (ml/min/1.73 m2) = 186 x (Serum Creatinine)-1.154 x (age in years)-0.023 x (0.742 if patient is female) x (1.212 if patient is black).
  8. Bilirubin <=2 times the upper limit of normal
  9. AST <=3 times the upper limit of normal

Donor criteria:

  1. HLA-Matched Sibling: The donor must be an adequate HLA match as determined by serologic typing for class (A, B) and low resolution molecular typing for class II (DRB1) as defined by institutional standards.
  2. Matched Unrelated Donor: An acceptable match per NMDP standards based on high resolution molecular typing.
  3. The donor must be healthy and must be an acceptable donor as per institutional standards for stem cell collection.
  4. The donor must have no significant cardiopulmonary, renal, endocrine, or hepatic disease.
  5. There is no upper age restriction for donors, but they must be at least 18 years of age.
  6. Syngeneic donors are not eligible.
  7. No known HIV.

Exclusion Criteria:

  1. Pregnant or nursing.
  2. Active systemic infection considered opportunistic, life threatening or clinically significant at the time of treatment.
  3. Severe concurrent disease, including severe insulin-dependent diabetes, uncontrolled hypertension, transient ischemic attacks, uncontrolled symptomatic coronary artery disease, or symptomatic CNS involvement or psychiatric illness/social situations that would limit compliance with study requirements.
  4. Known HIV disease.
  5. History of other malignancy except for basal cell or squamous cell carcinoma of the skin or carcinoma in situ of the cervix or breast unless the subject has been off treatment and free from disease for > 3 years.
  6. Active disease at the time of transplant.

Sites / Locations

  • Ravi Vij, M.D.

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Arm 1: Non-myeloablative conditioning regimen

Arm Description

Clofarabine 40mg/m2/day IV over two hours daily x 5 days on Days -6 thru -2 Cytarabine 1gm/m2/day IV over two hours daily x 5 days on Days -6 thru -2 after the START of Clofarabine. Thymoglobulin 1.0mg/kg IV over 6 hours X 1 day on Day -4, then 2.5mg/kg/day x 2 days on Days -3 and -2. Stem Cell Transplant - On day 0 a minimum of total CD34+ cell dose of 2 x10E6/kg (actual weight of recipient) will be infused.

Outcomes

Primary Outcome Measures

Six-month Treatment Related Mortality

Secondary Outcome Measures

Disease Specific Response Rates
Disease-specific partial response and complete response.
Engraftment as Measured by Percent Donor Chimerism
Engraftment as Measured by Percent Donor Chimerism
Engraftment as Measured by Percent Donor Chimerism
Overall Survival
Disease-free Survival
Disease-free survival is defined as the length of time after treatment ends that the participant survives without any signs or symptoms of that cancer.
Rate of Acute Graft-versus-host Disease (GVHD)
Acute GVHD occurs within 100 days of transplant.
Rate of Chronic Graft-versus-host Disease (GVHD)
Use Conventional STR-PCR Method for Monitoring Engraftment
Includes assessment of mixed chimerism in the whole blood, myeloid cells, T cells, and B cells.
Median Time to Progression
Time to progression is defined as the length of time from the start of treatment until the disease starts to get worse or spread to other parts of the body.

Full Information

First Posted
January 2, 2008
Last Updated
September 5, 2014
Sponsor
Washington University School of Medicine
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1. Study Identification

Unique Protocol Identification Number
NCT00593645
Brief Title
Clofarabine, Cytarabine, and Thymoglobulin for Allogeneic Transplantation
Official Title
A Non-Myeloablative Conditioning Regimen for Allogeneic Transplantation With Clofarabine, Cytarabine, and Thymoglobulin for Myelodysplastic Syndrome and Acute Myeloid Leukemia
Study Type
Interventional

2. Study Status

Record Verification Date
September 2014
Overall Recruitment Status
Terminated
Why Stopped
toxicities were worse than expected
Study Start Date
November 2007 (undefined)
Primary Completion Date
December 2008 (Actual)
Study Completion Date
July 2009 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Washington University School of Medicine

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This study will test the combination of clofarabine, cytarabine, and thymoglobulin as a non-myeloablative conditioning regimen for patients with myelodysplastic syndromes or acute myeloid leukemia undergoing allogeneic stem cell transplant.
Detailed Description
Current reduced intensity conditioning regimens have been able to decrease TRM (treatment related mortality) but suffer from increased rates of disease relapse. Disease burden at transplantation, as measured by percent myeloblasts, predicts relapse. Current regimens employ fludarabine and busulfan with various adjutants, but these agents are not part of the usual armamentarium used versus leukemia and have questionable anti-leukemic activity. By substituting clofarabine and cytarabine, a combination with proven anti-leukemic activity in the relapsed and refractory setting as well as activity versus MDS, as the back bone of the regimen we hope overcome residual disease and improve post-transplant relapse rates. Furthermore the principal toxicity of this regimen is myelosuppression, which should be abrogated by the infusion of stem cells. Thymoglobulin is included due to its minimal contribution to toxicity but significant benefits in engraftment, and controlling acute and chronic GVHD, which are major contributors to TRM and disease specific activity in MDS.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Myelodysplastic Syndromes, Acute Myeloid Leukemia
Keywords
Conditioning regimens, Stem Cell Transplantation, Hematopoietic Stem Cell Transplantation, Allogeneic Stem Cell Transplantation, Nonmyeloablative conditioning, Clofarabine, Cytarabine, Anti-thymocyte globulin

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
7 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Arm 1: Non-myeloablative conditioning regimen
Arm Type
Experimental
Arm Description
Clofarabine 40mg/m2/day IV over two hours daily x 5 days on Days -6 thru -2 Cytarabine 1gm/m2/day IV over two hours daily x 5 days on Days -6 thru -2 after the START of Clofarabine. Thymoglobulin 1.0mg/kg IV over 6 hours X 1 day on Day -4, then 2.5mg/kg/day x 2 days on Days -3 and -2. Stem Cell Transplant - On day 0 a minimum of total CD34+ cell dose of 2 x10E6/kg (actual weight of recipient) will be infused.
Intervention Type
Drug
Intervention Name(s)
Clofarabine
Other Intervention Name(s)
Clolar
Intervention Type
Drug
Intervention Name(s)
Cytarabine
Other Intervention Name(s)
Ara-C, Cytosar
Intervention Type
Drug
Intervention Name(s)
Thymoglobulin
Other Intervention Name(s)
Anti-thymocyte globulin
Intervention Type
Procedure
Intervention Name(s)
Stem cell infusion
Other Intervention Name(s)
Stem cell transplant, Hematopoietic stem cell transplant, Peripheral blood stem cell transplant, Bone marrow transplant
Primary Outcome Measure Information:
Title
Six-month Treatment Related Mortality
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Disease Specific Response Rates
Description
Disease-specific partial response and complete response.
Time Frame
One, three, six and twelve months.
Title
Engraftment as Measured by Percent Donor Chimerism
Time Frame
Day +30
Title
Engraftment as Measured by Percent Donor Chimerism
Time Frame
Day +40-+60
Title
Engraftment as Measured by Percent Donor Chimerism
Time Frame
Day +80-+90
Title
Overall Survival
Time Frame
5 years from time of restaging
Title
Disease-free Survival
Description
Disease-free survival is defined as the length of time after treatment ends that the participant survives without any signs or symptoms of that cancer.
Time Frame
5 years from time of restaging
Title
Rate of Acute Graft-versus-host Disease (GVHD)
Description
Acute GVHD occurs within 100 days of transplant.
Time Frame
Up to 100 days after transplant
Title
Rate of Chronic Graft-versus-host Disease (GVHD)
Time Frame
100 days-1 year after transplant
Title
Use Conventional STR-PCR Method for Monitoring Engraftment
Description
Includes assessment of mixed chimerism in the whole blood, myeloid cells, T cells, and B cells.
Time Frame
Up to 1 year after transplant
Title
Median Time to Progression
Description
Time to progression is defined as the length of time from the start of treatment until the disease starts to get worse or spread to other parts of the body.
Time Frame
5 years from time of restaging

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria (Patient): Myelodysplastic Syndrome (MDS), as defined by the World Health Organization criteria, OR Chronic Myelomonocytic Leukemia (CMML) as defined by the French American British classification OR Acute Myeloid Leukemia (AML) in complete remission [excluding FAB-M3] diagnosed by standard criteria and meet the criteria below: Patients may be in any CR No more than 2 cycles of consolidation. Any consolidation regimen may be used. No more than 6 months from documented CR to transplant. Age 18 years or older. ECOG performance status <=2 Identification of suitable donor DLCO >=40% with no symptomatic pulmonary disease LVEF by MUGA >= 30% Serum creatinine <=1.0 mg/dL; if serum creatinine >1.0 mg/dL, then the estimated glomerular filtration rate (GFR) must be >60 mL/min/1.73 m2 as calculated by the Modification of Diet in Renal Disease equation where Predicted GFR (ml/min/1.73 m2) = 186 x (Serum Creatinine)-1.154 x (age in years)-0.023 x (0.742 if patient is female) x (1.212 if patient is black). Bilirubin <=2 times the upper limit of normal AST <=3 times the upper limit of normal Donor criteria: HLA-Matched Sibling: The donor must be an adequate HLA match as determined by serologic typing for class (A, B) and low resolution molecular typing for class II (DRB1) as defined by institutional standards. Matched Unrelated Donor: An acceptable match per NMDP standards based on high resolution molecular typing. The donor must be healthy and must be an acceptable donor as per institutional standards for stem cell collection. The donor must have no significant cardiopulmonary, renal, endocrine, or hepatic disease. There is no upper age restriction for donors, but they must be at least 18 years of age. Syngeneic donors are not eligible. No known HIV. Exclusion Criteria: Pregnant or nursing. Active systemic infection considered opportunistic, life threatening or clinically significant at the time of treatment. Severe concurrent disease, including severe insulin-dependent diabetes, uncontrolled hypertension, transient ischemic attacks, uncontrolled symptomatic coronary artery disease, or symptomatic CNS involvement or psychiatric illness/social situations that would limit compliance with study requirements. Known HIV disease. History of other malignancy except for basal cell or squamous cell carcinoma of the skin or carcinoma in situ of the cervix or breast unless the subject has been off treatment and free from disease for > 3 years. Active disease at the time of transplant.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ravi Vij, M.D.
Organizational Affiliation
Washington Universtiy of St. Louis
Official's Role
Principal Investigator
Facility Information:
Facility Name
Ravi Vij, M.D.
City
St. Louis
State/Province
Missouri
ZIP/Postal Code
63110
Country
United States

12. IPD Sharing Statement

Links:
URL
http://www.siteman.wustl.edu
Description
Alvin J. Siteman Cancer Center at Barnes-Jewish Hospital and Washington University School of Medicine

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Clofarabine, Cytarabine, and Thymoglobulin for Allogeneic Transplantation

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