Addition of Gemcitabine to Pre Allo-HSCT Conditioning for Acute Lymphoblastic Leukemia
Primary Purpose
Acute Lymphoblastic Leukemia, Adult
Status
Unknown status
Phase
Phase 2
Locations
Mexico
Study Type
Interventional
Intervention
Gemcitabine
Busulfan
Cyclophosphamide
Allogeneic Hematopoietic Stem Cell Transplantation
Sponsored by
About this trial
This is an interventional treatment trial for Acute Lymphoblastic Leukemia, Adult
Eligibility Criteria
Inclusion Criteria:
- Diagnosis of acute lymphoblastic leukemia in 2nd complete remission or primary refractory disease, candidates to hematopoietic stem cell transplantation.
- Hemoglobin ≥ 10 g/dl, Absolute Neutrophil Count ≥ 1 x 103/mm3, and Platelets ≥ 100,000 /µL
- Eastern Cooperative Oncology Group status (ECOG) ≤2 oR Karnofsky ≥80%
- Signed Informed Consent
- Left ventricular ejection fraction (LVEF) >40%
- Normal liver function enzyme tests
- Preserved renal function
Exclusion Criteria:
- Patients not willing to participate or to sign the informed consent
- Patients who do not meet the inclusion criteria
Sites / Locations
- Instituto Nacional de Ciencias Medicas y Nutricion Salvador ZubiranRecruiting
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Unique
Arm Description
Patients will receive reduced Busulfan and Cyclophosphamide (BUCY 2) conditioning regimen, consisting in the administration of two medications: Busulfan and Cyclophosphamide Plus: Gemcitabine. Then patients will undergo an Allogeneic Hematopoietic Stem Cell Transplantation.
Outcomes
Primary Outcome Measures
Disease Free Survival
Time between transplantation and relapse or last follow-up
Secondary Outcome Measures
Overall Survival
Time between transplantation and dead or last follow-up
Full Information
NCT ID
NCT03339700
First Posted
November 8, 2017
Last Updated
January 10, 2020
Sponsor
Instituto Nacional de Ciencias Medicas y Nutricion Salvador Zubiran
1. Study Identification
Unique Protocol Identification Number
NCT03339700
Brief Title
Addition of Gemcitabine to Pre Allo-HSCT Conditioning for Acute Lymphoblastic Leukemia
Official Title
Addition of Gemcitabine to the Standard Reduced Busulfan and Cyclophosphamide (BUCY2) Pre Allogeneic Hematopoietic Stem Cell Transplantation Conditioning for Acute Lymphoblastic Leukemia
Study Type
Interventional
2. Study Status
Record Verification Date
January 2020
Overall Recruitment Status
Unknown status
Study Start Date
September 15, 2018 (Actual)
Primary Completion Date
September 2020 (Anticipated)
Study Completion Date
September 2021 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Instituto Nacional de Ciencias Medicas y Nutricion Salvador Zubiran
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
The main purpose of the project is to evaluate the disease free survival and overall survival in patients diagnosed with acute lymphoblastic leukemia undergoing allogeneic hematopoietic stem cell transplantation (allo-HSCT) adding gemcitabine to the standard institutional conditioning regimen based on two alkylating drugs, reduced busulfan and cyclophosphamide (reduced BUCY 2).
Detailed Description
In the last decade, hematopoietic stem cell transplantation (HSCT) has become an efficient strategy for the treatment of high risk acute lymphoblastic leukemias. Lymphoid acute leukemias (ALL) are considered malignant clonal diseases of the hematopoietic stem cells, and represent a therapeutic challenge due to the high relapse rate and mortality using conventional chemotherapy regimens. Many studies have shown a decrease in relapse and an increase in overall survival with allogeneic HSCT, however, despite the fact that results in ALL have improved in the past years, achieving complete remission (CR) in approximately 75% of the patients, the relapse rate remains high and long term survival is lower than 50% depending on age and disease characteristics. On the other hand, it has been stated that relapse is higher when an allo-HSCT is performed in second CR, obtaining poorer results compared to performing HSCT in first CR, although better than chemotherapy alone (87% probability of relapse).
It is necessary to implement strategies that increase efficiency of pre transplant conditioning regimens in patients diagnosed with ALL undergoing an allo-HSCT in order to reduce relapse and increase overall survival. The hypothesis is that adding gemcitabine to the standard institutional conditioning regimen (reduced BUCY 2) in patients with ALL undergoing an allo-HSCT, the relapse free survival as well as the overall survival will improve, because it has been demonstrated in other malignant hematological diseases that gemcitabine plus two alkylating agents, facilitates synergism with busulfan and melphalan, inhibiting the DNA damage repair and causing a higher cytotoxic effect.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Acute Lymphoblastic Leukemia, Adult
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
15 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Unique
Arm Type
Experimental
Arm Description
Patients will receive reduced Busulfan and Cyclophosphamide (BUCY 2) conditioning regimen, consisting in the administration of two medications: Busulfan and Cyclophosphamide Plus: Gemcitabine. Then patients will undergo an Allogeneic Hematopoietic Stem Cell Transplantation.
Intervention Type
Drug
Intervention Name(s)
Gemcitabine
Other Intervention Name(s)
Gemzar
Intervention Description
4800mg/m2, intravenous (IV), divided 4 days, 1200mg/m2/day, during days -5 to -2
Intervention Type
Drug
Intervention Name(s)
Busulfan
Other Intervention Name(s)
Myleran
Intervention Description
12mg/kg, Oral, divided in 4 days, 3mg/kg/day Oral, during days -7 to -4.
Intervention Type
Drug
Intervention Name(s)
Cyclophosphamide
Other Intervention Name(s)
Cytoxan
Intervention Description
80mg/kg, intravenous (IV), divided in 2 days, 40mg/kg/day IV, during days -3 and -2.
Intervention Type
Procedure
Intervention Name(s)
Allogeneic Hematopoietic Stem Cell Transplantation
Other Intervention Name(s)
Allogeneic Bone Marrow Transplantation
Intervention Description
Bone Marrow HSC (allogeneic HSCT) transfusion, day 0
Primary Outcome Measure Information:
Title
Disease Free Survival
Description
Time between transplantation and relapse or last follow-up
Time Frame
3 years
Secondary Outcome Measure Information:
Title
Overall Survival
Description
Time between transplantation and dead or last follow-up
Time Frame
5 years
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Diagnosis of acute lymphoblastic leukemia in 2nd complete remission or primary refractory disease, candidates to hematopoietic stem cell transplantation.
Hemoglobin ≥ 10 g/dl, Absolute Neutrophil Count ≥ 1 x 103/mm3, and Platelets ≥ 100,000 /µL
Eastern Cooperative Oncology Group status (ECOG) ≤2 oR Karnofsky ≥80%
Signed Informed Consent
Left ventricular ejection fraction (LVEF) >40%
Normal liver function enzyme tests
Preserved renal function
Exclusion Criteria:
Patients not willing to participate or to sign the informed consent
Patients who do not meet the inclusion criteria
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Eucario Leon Rodriguez, M.D.
Phone
525554870900
Ext
2255
Email
eucarios@hotmail.com
First Name & Middle Initial & Last Name or Official Title & Degree
Monica M Rivera Franco, M.D.,MSc
Phone
525554870900
Ext
2719
Email
monrif90d@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Eucario Leon Rodriguez, M.D.
Organizational Affiliation
Instituto Nacional de Ciencias Medicas y Nutricion Salvador Zubiran
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Monica M Rivera Franco, M.D.,MSc
Organizational Affiliation
Instituto Nacional de Ciencias Medicas y Nutricion Salvador Zubiran
Official's Role
Principal Investigator
Facility Information:
Facility Name
Instituto Nacional de Ciencias Medicas y Nutricion Salvador Zubiran
City
Mexico City
State/Province
Distrito Federal
ZIP/Postal Code
14080
Country
Mexico
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Eucario Leon Rodriguez, M.D.
Phone
525554870900
Ext
2255
Email
eucarios@hotmail.com
First Name & Middle Initial & Last Name & Degree
Monica M Rivera Franco, M.D.
Phone
525554870900
Ext
2719
Email
monrif90d@gmail.com
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
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22643322
Citation
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Results Reference
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Citation
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Addition of Gemcitabine to Pre Allo-HSCT Conditioning for Acute Lymphoblastic Leukemia
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