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Standard vs. Reduced-Intensity Conditioning in Patients With Acute Myeloid Leukemia in First Remission

Primary Purpose

Acute Myeloid Leukemia

Status
Terminated
Phase
Phase 3
Locations
Germany
Study Type
Interventional
Intervention
Conditioning therapy
Sponsored by
University Hospital Carl Gustav Carus
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Acute Myeloid Leukemia focused on measuring Reduced-intensity conditioning, Fludarabine, Acute myeloid Leukemia, Treatment-related mortality

Eligibility Criteria

18 Years - 60 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Diagnosis of acute myeloid leukemia in first remission Standard-or high-risk marrow cytogenetics HLA-matched related or unrelated donor available (in case of high-risk disease) Age 18 to 60 Informed consent Consent of donor to donate peripheral blood stem cells sufficient liver function (elevation of transferases < 2.5 x upper limit) Exclusion Criteria: AML with t(5;17) AML with t((8;21) clinically relevant heart failure (NYHA II-IV) Renal failure (creatinine > 200 µg/ml) Liver function failure (bilirubin > 3 mg/dl) Concomitant Neurological or psychiatric disease Contraindications to receive prescribed study medication HIV infection Pregnancy

Sites / Locations

  • Medizinische Klinik und Poliklinik I

Arms of the Study

Arm 1

Arm 2

Arm Type

Other

Experimental

Arm Label

12 Gy/Cyclophosphamide

8 Gy /Fludarabine

Arm Description

Standard intensity conditioning

Reduced-intensity conditioning

Outcomes

Primary Outcome Measures

Treatment-related mortality at 12 months after transplantation
Proportion of patients dying without prior relapse

Secondary Outcome Measures

Disease-free and Overall survival
Proportion of patients alive without relapse
Grade 3-4 extramedullary toxicity
Percentage of patients with grade II-IV acute GvHD

Full Information

First Posted
September 6, 2005
Last Updated
June 19, 2013
Sponsor
University Hospital Carl Gustav Carus
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1. Study Identification

Unique Protocol Identification Number
NCT00150878
Brief Title
Standard vs. Reduced-Intensity Conditioning in Patients With Acute Myeloid Leukemia in First Remission
Official Title
Randomized Phase III Comparison of 12 Gy TBI and Cyclophosphamide 120 mg/kg With Fludarabine 120 mg/Sqm and 8 Gy TBI Before Allogeneic Transplantation in Patients With Acute Myeloid Leukemia in First Remission
Study Type
Interventional

2. Study Status

Record Verification Date
June 2013
Overall Recruitment Status
Terminated
Why Stopped
Insurance coverage reached
Study Start Date
December 2003 (undefined)
Primary Completion Date
December 2009 (Actual)
Study Completion Date
December 2010 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
University Hospital Carl Gustav Carus

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The primary goal of the study is to show that the treatment-related mortality of allogeneic hematopoietic stem cell transplantation an be significantly reduced by using a combination of 8 Gy total-body-irradiation and fludarabine in comparison to the conventional combination of 12 Gy TBI and 120 mg/kg Cyclophosphamide.
Detailed Description
Transplant-related deaths because of extramedullary toxicity and graft-versus host disease remain the major causes for treatment-failure in patients with AMl receiving allogeneic hematopoietic stem cell transplantation. In phase II study, M . Stelljes and coworkers could show, that a reduced dose of total-body- irradiation and fludarabine can be safely used in patients with AML at various disease stages. The best results could be achieved in patients who had been in complete remission by the time of inclusion. Therefore this prospective trial was initiated to compare the new conditioning regimen with the standard regimen of 12 Gy TBI/Cyclophosphamide 120 mg/kg in patients ith AML in first remission. After having achieved complete remission, and giving informed consent, patients are stratified according to marrow cytogenetics, age and type of induction therapy and subsequently randomized to receive on of the mentioned conditioning therapies. The primary end-point will be non-relapse mortality. The hypothesis would be, that the one-year mortality can be reduced from 25 to 15%. Given a power of 0.8 and a first-error of 5%, 252 patients will have to be randomized. Secondary endpoints include: 3 year overall-and disease-free survival Rate of grade II-IV acute GvHD Rate of grade 3-4 extramedullary toxicity

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Acute Myeloid Leukemia
Keywords
Reduced-intensity conditioning, Fludarabine, Acute myeloid Leukemia, Treatment-related mortality

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
198 (Actual)

8. Arms, Groups, and Interventions

Arm Title
12 Gy/Cyclophosphamide
Arm Type
Other
Arm Description
Standard intensity conditioning
Arm Title
8 Gy /Fludarabine
Arm Type
Experimental
Arm Description
Reduced-intensity conditioning
Intervention Type
Other
Intervention Name(s)
Conditioning therapy
Intervention Description
Preparation before allogeneic transplantation
Primary Outcome Measure Information:
Title
Treatment-related mortality at 12 months after transplantation
Description
Proportion of patients dying without prior relapse
Time Frame
12 months
Secondary Outcome Measure Information:
Title
Disease-free and Overall survival
Description
Proportion of patients alive without relapse
Time Frame
5 years
Title
Grade 3-4 extramedullary toxicity
Description
Percentage of patients with grade II-IV acute GvHD
Time Frame
100 days

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 myeloid leukemia in first remission Standard-or high-risk marrow cytogenetics HLA-matched related or unrelated donor available (in case of high-risk disease) Age 18 to 60 Informed consent Consent of donor to donate peripheral blood stem cells sufficient liver function (elevation of transferases < 2.5 x upper limit) Exclusion Criteria: AML with t(5;17) AML with t((8;21) clinically relevant heart failure (NYHA II-IV) Renal failure (creatinine > 200 µg/ml) Liver function failure (bilirubin > 3 mg/dl) Concomitant Neurological or psychiatric disease Contraindications to receive prescribed study medication HIV infection Pregnancy
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Gerhard Ehninger, MD
Organizational Affiliation
Director of Med. Klink und Poliklinik I, Technical University Dresden
Official's Role
Study Director
Facility Information:
Facility Name
Medizinische Klinik und Poliklinik I
City
Dresden
ZIP/Postal Code
01307
Country
Germany

12. IPD Sharing Statement

Citations:
PubMed Identifier
16020510
Citation
Stelljes M, Bornhauser M, Kroger M, Beyer J, Sauerland MC, Heinecke A, Berning B, Scheffold C, Silling G, Buchner T, Neubauer A, Fauser AA, Ehninger G, Berdel WE, Kienast J; Cooperative German Transplant Study Group. Conditioning with 8-Gy total body irradiation and fludarabine for allogeneic hematopoietic stem cell transplantation in acute myeloid leukemia. Blood. 2005 Nov 1;106(9):3314-21. doi: 10.1182/blood-2005-04-1377. Epub 2005 Jul 14.
Results Reference
background
PubMed Identifier
29550384
Citation
Fasslrinner F, Schetelig J, Burchert A, Kramer M, Trenschel R, Hegenbart U, Stadler M, Schafer-Eckart K, Batzel M, Eich H, Stuschke M, Engenhart-Cabillic R, Krause M, Dreger P, Neubauer A, Ehninger G, Beelen D, Berdel WE, Siepmann T, Stelljes M, Bornhauser M. Long-term efficacy of reduced-intensity versus myeloablative conditioning before allogeneic haemopoietic cell transplantation in patients with acute myeloid leukaemia in first complete remission: retrospective follow-up of an open-label, randomised phase 3 trial. Lancet Haematol. 2018 Apr;5(4):e161-e169. doi: 10.1016/S2352-3026(18)30022-X. Epub 2018 Mar 14.
Results Reference
derived
PubMed Identifier
22959335
Citation
Bornhauser M, Kienast J, Trenschel R, Burchert A, Hegenbart U, Stadler M, Baurmann H, Schafer-Eckart K, Holler E, Kroger N, Schmid C, Einsele H, Kiehl MG, Hiddemann W, Schwerdtfeger R, Buchholz S, Dreger P, Neubauer A, Berdel WE, Ehninger G, Beelen DW, Schetelig J, Stelljes M. Reduced-intensity conditioning versus standard conditioning before allogeneic haemopoietic cell transplantation in patients with acute myeloid leukaemia in first complete remission: a prospective, open-label randomised phase 3 trial. Lancet Oncol. 2012 Oct;13(10):1035-44. doi: 10.1016/S1470-2045(12)70349-2. Epub 2012 Sep 7.
Results Reference
derived
Links:
URL
http://www.kompetenznetz-leukaemie.de/
Description
Central Leukemia Study Group

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Standard vs. Reduced-Intensity Conditioning in Patients With Acute Myeloid Leukemia in First Remission

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