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Randomized Study of Conditioning of Fludarabine Combined With Single or Dual Alkylating Agents in Myeloid Malignancies

Primary Purpose

Acute Myeloid Leukemia, Myelodysplastic Syndromes

Status
Recruiting
Phase
Phase 3
Locations
China
Study Type
Interventional
Intervention
Fludarabine, busulfan and melphalan
Fludarabine and Busulfan
Sponsored by
Shanghai Jiao Tong University School of Medicine
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Acute Myeloid Leukemia focused on measuring conditioning regimen, melphalan, busulfan, fludarabine

Eligibility Criteria

16 Years - 55 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: acute myeloid leukemia (acute promyelocytic leukemia excluded) in 1st complete remission myelodysplasia syndrome with bone marrow blast >5% and remaining less than 20% at transplantation patients with HLA matched sibling donor, 9-10 matched unrelated donor or haplo-identical related donors inform consent provided Exclusion Criteria: AML patients with active CNS or extramedullary diseases patients with active viral, bacterial or fungal infection patients with hepatitis B virus >1X103 copy/ml patients with abnormal liver function, renal function, respiratory or cardiac dysfunction patients with uncontrolled mental disorders patients with HIV

Sites / Locations

  • Fujian Medical University Union HospitalRecruiting
  • Zhongshan Hospital, Xianmen UniversityRecruiting
  • 923th Hospital PLARecruiting
  • First Affiliatied Hospital of Soochow UniversityRecruiting
  • First Affiliated Hospital of Nanjin Medical UnviersityRecruiting
  • Ruijin HospitalRecruiting
  • Shanghai No10 HospitalRecruiting
  • 920th Hospital PLARecruiting
  • Shanghai No 6 HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Flu-Bu2-Mel140

Flu-Bu4

Arm Description

Patients receive fludarabine, busulfan and melphalan as conditioning regimen

Patients receive fludarabine and busulfan as conditioning regimen

Outcomes

Primary Outcome Measures

disease-free survival
event defined as relapse and death of any causes

Secondary Outcome Measures

overall survival
event defined as death of any causes
incidence of relapse
event defined as disease relapse (bone marrow or extra medullary)
non relapse mortality
event defined as death without disease relapse
non relapse mortality
event defined as death without disease relapse

Full Information

First Posted
August 8, 2023
Last Updated
October 21, 2023
Sponsor
Shanghai Jiao Tong University School of Medicine
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1. Study Identification

Unique Protocol Identification Number
NCT05991908
Brief Title
Randomized Study of Conditioning of Fludarabine Combined With Single or Dual Alkylating Agents in Myeloid Malignancies
Official Title
Multiple-center Randomized Study to Compare Fludarabine and Busulfan Versus Fludarabine, Busulfan and Melphalan in Adult Patients With Acute Myeloid Leukemia (AML) and Myelodysplasia Syndrome (MDS)
Study Type
Interventional

2. Study Status

Record Verification Date
October 2023
Overall Recruitment Status
Recruiting
Study Start Date
October 19, 2023 (Actual)
Primary Completion Date
October 30, 2025 (Anticipated)
Study Completion Date
June 30, 2026 (Anticipated)

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
Yes

5. Study Description

Brief Summary
Fludarabine and busulfan becomes standard conditioning regimen for adult patients with acute myeloid leukemia (AML) or myelodysplasia syndrome (MDS). The overall relapse rate is 15~20%. More recently, the investigators demonstrated that conditioning regimen with dual alkylating agents consistent of fludarabine, busulfan and melphalan achieved a low incidence of relapse (<10%). This multiple-center randomize study is aim to compare the transplantation outcome in adult patients with AML/MDS undergoing allo-HSCT with conditioning regimen of Flu-Bu4 vs. FLu-Bu-Mel.
Detailed Description
Fludarabine and busulfan was considered as myeloablative but reduced toxicity regimen and became as the mainstay of conditioning regimen for adult patients with acute myeloid leukemia (AML) or myelodysplasia syndrome (MDS). The disease relapse remained as major cause of treatment failure. In general, the cumulated incidence of relapse (CIR) is about 15~20% dependent on the risk of patients undergoing allogeneic stem cell transplantation (allo-HSCT). Conditioning regimen with dual alkylating agents such as fludarabine, busulfan and thiotepa (TBF) showed decreased risk of relapse in myeloid malignancies. More recently, the investigators demonstrated that conditioning regimen with dual alkylating agents consistent of fludarabine, busulfan and melphalan could achieve a low incidence of relapse (2 year CIR <10%). In this multiple-center randomize study, the aim is to compare the transplantation outcome in adult patients with AML/MDS undergoing allo-HSCT with conditioning regimen of Flu-Bu vs. Flu-Bu-Mel.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Acute Myeloid Leukemia, Myelodysplastic Syndromes
Keywords
conditioning regimen, melphalan, busulfan, fludarabine

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Model Description
study group with fludarabine, busulfan and melphalan regimen versus control group with fludarabine and busulfan
Masking
None (Open Label)
Allocation
Randomized
Enrollment
222 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Flu-Bu2-Mel140
Arm Type
Experimental
Arm Description
Patients receive fludarabine, busulfan and melphalan as conditioning regimen
Arm Title
Flu-Bu4
Arm Type
Active Comparator
Arm Description
Patients receive fludarabine and busulfan as conditioning regimen
Intervention Type
Drug
Intervention Name(s)
Fludarabine, busulfan and melphalan
Intervention Description
FLudarabine 150mg/m2 + Busulfan 6.4mg.kg + Mel 140mg/m2
Intervention Type
Drug
Intervention Name(s)
Fludarabine and Busulfan
Intervention Description
FLudarabine 150mg/m2 + Busulfan 12.8mg.kg
Primary Outcome Measure Information:
Title
disease-free survival
Description
event defined as relapse and death of any causes
Time Frame
2 year
Secondary Outcome Measure Information:
Title
overall survival
Description
event defined as death of any causes
Time Frame
2 year
Title
incidence of relapse
Description
event defined as disease relapse (bone marrow or extra medullary)
Time Frame
2 year
Title
non relapse mortality
Description
event defined as death without disease relapse
Time Frame
day 100
Title
non relapse mortality
Description
event defined as death without disease relapse
Time Frame
2 year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
16 Years
Maximum Age & Unit of Time
55 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: acute myeloid leukemia (acute promyelocytic leukemia excluded) in 1st complete remission myelodysplasia syndrome with bone marrow blast >5% and remaining less than 20% at transplantation patients with HLA matched sibling donor, 9-10 matched unrelated donor or haplo-identical related donors inform consent provided Exclusion Criteria: AML patients with active CNS or extramedullary diseases patients with active viral, bacterial or fungal infection patients with hepatitis B virus >1X103 copy/ml patients with abnormal liver function, renal function, respiratory or cardiac dysfunction patients with uncontrolled mental disorders patients with HIV
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
chun Wang
Phone
13386259777
Email
wangchunsh@126.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Chun Wang
Organizational Affiliation
Go Broad Health Center, Zhaxin Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Fujian Medical University Union Hospital
City
Fuzhou
State/Province
Fujian
ZIP/Postal Code
350001
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Xiaofan Li
Phone
8618250490368
Email
morningshiplee@sina.cn
Facility Name
Zhongshan Hospital, Xianmen University
City
Xiamen
State/Province
Fujian
ZIP/Postal Code
361004
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
quanyi Lu
Phone
8613300959425
Email
luquanyi@xmu.edu.cn
Facility Name
923th Hospital PLA
City
Nanning
State/Province
Guangxi
ZIP/Postal Code
530021
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Xiaolin Yin
Phone
8613321717899
Email
280662268@qq.com
Facility Name
First Affiliatied Hospital of Soochow University
City
Suzhou
State/Province
Jiang Su
ZIP/Postal Code
215006
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Xiaojin Wu
Phone
861305749353
Email
wuxiaojin@suda.edu.cn
Facility Name
First Affiliated Hospital of Nanjin Medical Unviersity
City
Nanjin
State/Province
Jiangsu
ZIP/Postal Code
210029
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Kourong Miao
Phone
8613813828314
Email
kourongmiao@163.com
Facility Name
Ruijin Hospital
City
Shanghai
State/Province
Shanghai
ZIP/Postal Code
200025
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jiong HU
Phone
8613764313546
Email
hj10709@rjh.com.cn
Facility Name
Shanghai No10 Hospital
City
Shanghai
State/Province
Shanghai
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Houcai Wang
Phone
8618019498303
Email
houcaiwang@163.com
Facility Name
920th Hospital PLA
City
Kunming
ZIP/Postal Code
650000
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Xiaoping Li
Phone
8618523894353
Email
xiaopinllli@163.com
Facility Name
Shanghai No 6 Hospital
City
Shanghai
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
ChunKang Chang
Phone
8618930177640
Email
changchunkang0710@aliyun.com

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Randomized Study of Conditioning of Fludarabine Combined With Single or Dual Alkylating Agents in Myeloid Malignancies

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