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AML2003 - Standard-Therapy vs Intensified Therapy for Adult Acute Myeloid Leukemia Patients <= 60 Years

AML2003 - Randomized Comparison Between Standard-Therapy and Intensified Therapy for Adult Acute Myeloid Leukemia Patients <= 60 Years. A Prospective, Randomized, Multi-center Therapy-Optimizing-Study.

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00180102
Enrollment
600
Registered
2005-09-16
Start date
2003-12-31
Completion date
2009-11-30
Last updated
2009-12-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Leukemia, Nonlymphocytic, Acute

Keywords

acute myeloid leukemia, risk adapted treatment, early allogeneic stem cell transplantation, autologous stem cell transplantation

Brief summary

AML2003 is a prospective randomized trial, to investigate the value of early allogeneic stem cell transplantation in aplasia after induction therapy for high risk patients with acute myeloid leukemia.

Detailed description

AML2003 is a prospective randomized trial, to investigate the value of early allogeneic stem cell transplantation in aplasia after induction therapy for high risk patients with acute myeloid leukemia. A rapid analysis of risk-factors (cytogenetics, FLT3 status, clearance of blasts after first induction) and the donor situation is of utmost importance. For this fast search diagnostic, which is accomplished in all enclosed patients, significant resources are provided, to take the load off the participating centers. Furthermore, the relevance of autologous transplantation and the benefit of additional substances within the postremission therapy such as m-AMSA or mitoxantrone will be investigated. There is an up-front randomisation in four therapy arms with two cross-classifying factors of two stages (intensified vs. standard therapy and Ara C vs. Ara C+ mitoxantrone + m-AMSA). Thus, the intergroup treatment schedule of the German Competence Network is integrated into the AML2003 study as a central element and 25% of the patients are treated accordingly. In the intensified therapy arms a risk-adapted and priority-based therapy is implemented, including early allogeneic and consolidating autologous stem cell transplantation, respectively. In addition to the clinical questions , a detailed concomitant research program was initiated for the AML2003 study, to get a better view of the heterogeneity of AML and to open new ways for custom-made therapies.

Interventions

DRUGCytarabine vs. Cytarabine+Amsacrine+Mitoxantrone
PROCEDUREearly allogeneic PBSCT within induction therapy
PROCEDUREautologous PBSCT

Sponsors

Technische Universität Dresden
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
FACTORIAL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
16 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

* de novo or secondary acute myeloid leukemia FAB-subtypes M0-M2 and M4-M7 * de novo or secondary myelodysplastic syndrome WHO-type RAEB-2 * age 16 to 60 years * written informed consent

Exclusion criteria

* severe comorbidities * severe, uncontrolled complications of the leukemia * prior therapy for AML/MDS * other simultaneous hematological malignancies * HIV-Infection * known allergies against study medication * pregnancy * missing written informed consent

Design outcomes

Primary

MeasureTime frame
overall survival
relapse-free survival

Secondary

MeasureTime frame
complete remission rate after induction therapy
subgroup-analyses within the primary outcomes according to different risk factors
development of explanatory proportional hazard-models

Countries

Germany

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 27, 2026