The concept of the investigators risk-adapted multicenter treatment trial for younger adults, AML HD98A, is based on the results of the AML HD93 trial and on published data. Definition of risk groups is different compared to the AML HD93 trial; high-risk: refractory disease after first induction therapy and/or high risk karyotype \[abn(3q), -5/5q-, -7/7q-, abn(12p), abn(17p), complex\]; intermediate-risk: complete remission after induction therapy and intermediate risk karyotype \[normal, abn(11q23), abn(16q22), other rare aberrations\]; low-risk: complete remission after induction therapy and low risk karyotype \[t(8;21)\]. Patients exhibiting a t(15;17) were treated in a separated trial (APL HD95). Treatment consists of a first induction therapy with ICE followed by a second cycle ICE in case of response to first induction therapy. Patients with refractory disease after first induction therapy are assigned to a salvage therapy with A-HAM (all-trans retinoic acid, high-dose cytarabine and mitoxantrone) and the search for potential hematopoietic stem cell donors is extended from the family to unrelated persons. All patients achieving a CR after induction therapy with ICE are assigned to a first consolidation therapy with HAM. For intermediate-risk patients a peripheral stem cell or a bone marrow harvest are intended during the hematological recovery after the first consolidation. Second consolidation therapy was stratified according to the risk definition. For high risk patients a allogeneic transplantation is assigned from a related or unrelated donor preferentially after a dose-intensified conditioning therapy. All patients with intermediate risk and an HLA-matched family donor are assigned to allogeneic transplantation. Intermediate-risk patients without a family donor and normal karyotype at diagnosis are randomized between an autologous stem cell transplantation and a second course of HAM. The other intermediate-risk patients are assigned to autologous transplantation. For low-risk patients a second course of HAM is assigned.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
400
Department of Hematology / Oncology, University Hospital of Innsbruck
Innsbruck, Austria
III Medical Department, Hematology and Oncology Center, Hanuschhospital Wien
Vienna, Austria
Department of General Internal Medicine, University Hospital of Bonn
Bonn, Germany
Department of Internal Medicine Hematology, Heinrich-Heine University
Düsseldorf, Germany
Department of Interial Medicine III, City Hospital Frankfurt Am Main - Höchst
Frankfurt, Germany
Medical Department IV, University of Gießen
Giessen, Germany
Department of Interial Medicine, Wilhelm-Anton-Hospital Goch
Goch, Germany
Centre of Interial Medicine, University of Göttingen
Göttingen, Germany
Medical Department III of Hematology and Oncology, General Hospital Altona
Hamburg, Germany
Department of Interial Medicine V, University of Heidelberg
Heidelberg, Germany
...and 12 more locations
relapse-free survival
Time frame: two years
overall survival
Time frame: two years
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