CLAGE Sequential With Flu-Bu Conditioning for Refractory Acute Leukemia
Primary Purpose
Refractory Hematologic Cancer, Allogeneic Stem Cell Transplantation
Status
Completed
Phase
Phase 2
Locations
China
Study Type
Interventional
Intervention
CLAGE-FluBu
Sponsored by
About this trial
This is an interventional treatment trial for Refractory Hematologic Cancer
Eligibility Criteria
Inclusion Criteria:
- refractory myeloid malignancies including acute myeloid leukemia (AML) or chronic myeloid leukemia in blastic crisis (CML-BC)
- HLA matched sibling,unrelated donor, or haplo-identical donor
- Patients with bone marrow blast >5% and positive measurable disease via flowcytometry or PCR.
Exclusion Criteria:
- patients with active infection
- liver function damage: ALT/AST above 2X normal range; and renal function damage Scr>160µmol/L; insufficient pulmonary function (FEV1,FVC,DLCO<50%)and heart failure or with EF <50%
- mental instability
- unwilling to give inform consent
Sites / Locations
- Blood & Marrow Transplantation Center, RuiJin Hospital
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
treatment
Arm Description
Patients receive the study protocol: CLAGE sequential with Flu-Bu as conditioning regimen followed by low-dose decitabine maintenance
Outcomes
Primary Outcome Measures
leukemia-free survival
From enrollment to any event as relapse or death
Secondary Outcome Measures
overall survival
From enrollment to death
relapse rate
From enrollment to documentation of relapse
non relapse mortality
From enrollment to documentation of death without evidence of leukemia
Full Information
NCT ID
NCT03882203
First Posted
March 18, 2019
Last Updated
August 14, 2023
Sponsor
Shanghai Jiao Tong University School of Medicine
1. Study Identification
Unique Protocol Identification Number
NCT03882203
Brief Title
CLAGE Sequential With Flu-Bu Conditioning for Refractory Acute Leukemia
Official Title
Cladribine With Intermediate Cytarabine, G-CSF and VP16 Sequential With Fludarabine and Busulifan as Condoning Regimen for Refractory Acute Leukemia
Study Type
Interventional
2. Study Status
Record Verification Date
August 2023
Overall Recruitment Status
Completed
Study Start Date
August 1, 2018 (Actual)
Primary Completion Date
August 30, 2021 (Actual)
Study Completion Date
December 30, 2022 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Shanghai Jiao Tong University School of Medicine
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
For patients with refractory acute leukemia, allogeneic stem cell transplantation is the only curative therapy. Only 20% of patients may achieve long-term survival mostly due to relapse or nor-relapse mortality (NRM). In previous study, we demonstrated that intensive leukemia debulking chemotherapy FLAG-IDA sequential with Flu-BU conditioning is feasible with ~40% long-term survival. In the study, we further modified the chemotherapy with cladribine replacing fludarabine aiming a more potent anti-leukemia effect. Meanwhile, we reduce the dose of busulfan for patients with poor performance status and age over 45 aim to reduce the NRM. All patients will also receive post-transplantation maintenance therapy with low-dose decitabine to prevent relapse.
Detailed Description
For patients with refractory acute leukemia, allogeneic stem cell transplantation is the only curative therapy. Only 20% of patients may achieve long-term survival mostly due to relapse or nor-relapse mortality (NRM). In previous study, we demonstrated that intensive leukemia debulking chemotherapy FLAG-IDA sequential with Flu-BU conditioning is feasible with ~40% long-term survival. The most important cause of treatment failures were relapse and non-relpase mortality. The further analysis demonstrated that patients with higher bone marrow blast before allo-HSCT was associated with treatment failure and patients with poor perforce status or age over 45 had increased rate of NRM. To further optimization the protocol, we modified the chemotherapy with cladribine replacing fludarabine aiming a more potent anti-leukemia effect and replace idarubicin with VP-16. All patients will also receive post-transplantation maintenance therapy with low-dose decitabine (5mg/m2 daily for 5 days) to prevent the further reduce the relapse incidence. We anticipate LFS at 1 year should be above 50% and 1-year LFS of 20% is considered unacceptable.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Refractory Hematologic Cancer, Allogeneic Stem Cell Transplantation
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
18 (Actual)
8. Arms, Groups, and Interventions
Arm Title
treatment
Arm Type
Experimental
Arm Description
Patients receive the study protocol: CLAGE sequential with Flu-Bu as conditioning regimen followed by low-dose decitabine maintenance
Intervention Type
Drug
Intervention Name(s)
CLAGE-FluBu
Intervention Description
Cladribine combined with cytarabine and VP16 sequential with Fludarabine combined with busulifan
Primary Outcome Measure Information:
Title
leukemia-free survival
Description
From enrollment to any event as relapse or death
Time Frame
1 year
Secondary Outcome Measure Information:
Title
overall survival
Description
From enrollment to death
Time Frame
1 year
Title
relapse rate
Description
From enrollment to documentation of relapse
Time Frame
1 year
Title
non relapse mortality
Description
From enrollment to documentation of death without evidence of leukemia
Time Frame
1 year
10. Eligibility
Sex
All
Minimum Age & Unit of Time
16 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
refractory myeloid malignancies including acute myeloid leukemia (AML) or chronic myeloid leukemia in blastic crisis (CML-BC)
HLA matched sibling,unrelated donor, or haplo-identical donor
Patients with bone marrow blast >5% and positive measurable disease via flowcytometry or PCR.
Exclusion Criteria:
patients with active infection
liver function damage: ALT/AST above 2X normal range; and renal function damage Scr>160µmol/L; insufficient pulmonary function (FEV1,FVC,DLCO<50%)and heart failure or with EF <50%
mental instability
unwilling to give inform consent
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Junming Li, M.D
Organizational Affiliation
Department of Hematology, Rui Jin Hospital
Official's Role
Study Director
Facility Information:
Facility Name
Blood & Marrow Transplantation Center, RuiJin Hospital
City
Shanghai
ZIP/Postal Code
200025
Country
China
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
CLAGE Sequential With Flu-Bu Conditioning for Refractory Acute Leukemia
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