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

T

Technische Universität Dresden

Status and phase

Completed
Phase 4

Conditions

Leukemia, Nonlymphocytic, Acute

Treatments

Procedure: early allogeneic PBSCT within induction therapy
Drug: Cytarabine vs. Cytarabine+Amsacrine+Mitoxantrone
Procedure: autologous PBSCT

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

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.

Full 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.

Enrollment

600 estimated patients

Sex

All

Ages

16 to 60 years old

Volunteers

No Healthy Volunteers

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

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Factorial Assignment

Masking

None (Open label)

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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