NOPHO-AML 2004 Study for Children With Acute Myeloid Leukemia
Primary Purpose
Acute Myeloid Leukemia
Status
Completed
Phase
Phase 3
Locations
Denmark
Study Type
Interventional
Intervention
Gemtuzumab ozogamicin
Sponsored by

About this trial
This is an interventional treatment trial for Acute Myeloid Leukemia focused on measuring AML, Children, Gemtuzumab ozogamicin, Stem cell transplantation
Eligibility Criteria
Inclusion Criteria:
- AML as defined by the diagnostic criteria,
- Age < 19 years at time of study entry,
- Written informed consent
Exclusion Criteria:
- Previous chemo- or radiotherapy,
- AML secondary to previous bone marrow failure syndrome,
- Down syndrome (DS),
- Acute promyelocytic leukemia (APL),
- Juvenile myelomonocytic leukemia (JMML),
- Myelodysplastic syndrome (MDS),
- Fanconi anemia,
- Positive pregnancy test
Sites / Locations
- Department of Pediatrics, Aarhus University Hospital Skejby
- Rigshospitalet
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
No Intervention
Arm Label
1
2
Arm Description
Gemtuzumab 5 mg / m2 two courses with three week interval
No further therapy
Outcomes
Primary Outcome Measures
Event free survival
Secondary Outcome Measures
Overall survival
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT00476541
Brief Title
NOPHO-AML 2004 Study for Children With Acute Myeloid Leukemia
Official Title
NOPHO-AML 2004 Study for Children With Acute Myeloid Leukemia
Study Type
Interventional
2. Study Status
Record Verification Date
May 2015
Overall Recruitment Status
Completed
Study Start Date
January 2004 (undefined)
Primary Completion Date
January 2012 (Actual)
Study Completion Date
January 2012 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Aarhus
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The overall objective is to improve the cure rate of children with newly diagnosed acute myeloid leukemia (AML) who undergo risk-adapted therapy.
Stem cell transplantation (SCT) is reserved to high-risk patients defined by cytogenetics and response to chemotherapy. The efficacy and toxicity of Gemtuzumab ozogamicin (GO, Mylotarg) will be evaluated.
Detailed Description
The overall objective is to improve the cure rate of pediatric patients with newly diagnosed acute myeloid leukemia (AML). The specific aims are as follows:
1.1 Therapeutic aims
To improve the event-free survival (EFS) of AML patients who undergo risk-adapted therapy.
To improve the overall survival (OS) by reserving stem cell transplantation (SCT) to high-risk patients based on cytogenetics and response to induction therapy.
To compare the outcome of SCT using HLA-matched sibling donor (MSD) or HLA-matched unrelated donor (MUD).
To assess the efficacy and toxicity of Gemtuzumab ozogamicin (GO, Mylotarg) as post consolidation therapy.
1.2 Biologic aims
To study minimal residual disease (MRD) levels in blood and bone marrow (BM) at defined time points and to study the prognostic impact of MRD.
To test in vitro cellular drug resistance at diagnosis and relapse, and correlate these data to background factors and clinical outcome.
To secure storage of biological material from diagnosis for future biologic studies
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Acute Myeloid Leukemia
Keywords
AML, Children, Gemtuzumab ozogamicin, Stem cell transplantation
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
250 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
1
Arm Type
Experimental
Arm Description
Gemtuzumab 5 mg / m2 two courses with three week interval
Arm Title
2
Arm Type
No Intervention
Arm Description
No further therapy
Intervention Type
Drug
Intervention Name(s)
Gemtuzumab ozogamicin
Other Intervention Name(s)
Mylotarg
Intervention Description
Two courses of Gemtuzumab vs. no further therapy
Primary Outcome Measure Information:
Title
Event free survival
Time Frame
5 years
Secondary Outcome Measure Information:
Title
Overall survival
Time Frame
5 years
10. Eligibility
Sex
All
Minimum Age & Unit of Time
1 Day
Maximum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
AML as defined by the diagnostic criteria,
Age < 19 years at time of study entry,
Written informed consent
Exclusion Criteria:
Previous chemo- or radiotherapy,
AML secondary to previous bone marrow failure syndrome,
Down syndrome (DS),
Acute promyelocytic leukemia (APL),
Juvenile myelomonocytic leukemia (JMML),
Myelodysplastic syndrome (MDS),
Fanconi anemia,
Positive pregnancy test
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Henrik Hasle, MD
Organizational Affiliation
Department of Pediatrics, Aarhus University Hospital Skejby, Aarhus, Denmark
Official's Role
Study Chair
Facility Information:
Facility Name
Department of Pediatrics, Aarhus University Hospital Skejby
City
Aarhus
ZIP/Postal Code
8200
Country
Denmark
Facility Name
Rigshospitalet
City
Copenhagen
ZIP/Postal Code
2100
Country
Denmark
12. IPD Sharing Statement
Citations:
PubMed Identifier
16304571
Citation
Lie SO, Abrahamsson J, Clausen N, Forestier E, Hasle H, Hovi L, Jonmundsson G, Mellander L, Siimes MA, Yssing M, Zeller B, Gustafsson G; Nordic Society of Pediatric Hematology and Oncology (NOPHO); AML Study Group. Long-term results in children with AML: NOPHO-AML Study Group--report of three consecutive trials. Leukemia. 2005 Dec;19(12):2090-100. doi: 10.1038/sj.leu.2403962.
Results Reference
background
PubMed Identifier
12846889
Citation
Lie SO, Abrahamsson J, Clausen N, Forestier E, Hasle H, Hovi L, Jonmundsson G, Mellander L, Gustafsson G. Treatment stratification based on initial in vivo response in acute myeloid leukaemia in children without Down's syndrome: results of NOPHO-AML trials. Br J Haematol. 2003 Jul;122(2):217-25. doi: 10.1046/j.1365-2141.2003.04418.x.
Results Reference
background
PubMed Identifier
22730539
Citation
Hasle H, Abrahamsson J, Forestier E, Ha SY, Heldrup J, Jahnukainen K, Jonsson OG, Lausen B, Palle J, Zeller B; Nordic Society of Paediatric Haematology and Oncology (NOPHO). Gemtuzumab ozogamicin as postconsolidation therapy does not prevent relapse in children with AML: results from NOPHO-AML 2004. Blood. 2012 Aug 2;120(5):978-84. doi: 10.1182/blood-2012-03-416701. Epub 2012 Jun 22.
Results Reference
derived
Learn more about this trial
NOPHO-AML 2004 Study for Children With Acute Myeloid Leukemia
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