Open label, randomised, phase III multicenter trial.
* Arm I: * Induction therapy: Patients receive oral tretinoin twice daily and arsenic trioxide IV over 2 hours on days 1-60. Patients achieving hematological complete remission go on to receive consolidation therapy. * Consolidation therapy: Patients receive oral tretinoin twice daily on days 1-14. Treatment with tretinoin repeats every 4 weeks for up to 7 courses. Patients also receive arsenic trioxide IV over 2 hours on days 1-5 in weeks 1-4. Treatment with arsenic trioxide repeats every 8 weeks for up to 4 courses. * Arm II: * Induction therapy: Patients receive tretinoin as in arm I induction therapy and idarubicin IV over 20 minutes on days 2, 4, 6, and 8. Patients achieving hematological complete remission go on to receive consolidation therapy. * Consolidation therapy: Patients receive oral tretinoin twice daily on days 1-45, idarubicin IV over 20 minutes on days 1-4 and day 31, and mitoxantrone hydrochloride IV over 30 minutes on days 16-20. Marrow samples are collected after completion of consolidation therapy and analyzed by reverse transcriptase-PCR for molecular remission. Patients achieving molecular remission (PML-RARa negative) go on to receive maintenance therapy. * Maintenance therapy: Patients receive oral mercaptopurine once daily and methotrexate intramuscularly once weekly for 3 months. Treatment with mercaptopurine and methotrexate repeats every 3 months for 7 courses. After completion of course 1 of mercaptopurine and methotrexate, patients receive oral tretinoin once daily on days 1-15\*. Treatment with tretinoin repeats every 3 months for 6 courses. NOTE: \*Patients do not receive mercaptopurine and methotrexate during tretinoin administration. After completion of study therapy, patients are followed periodically for 5 years. As of 14th September 2010, all patients needed to evaluate the primary endpoint (162 patients) have been recruited but the trial accrual continued in order to assess one secondary outcome (QoL)."
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
276
Induction Arsenic Trioxide (As2O3=ATO), 0.15 mg/Kg IV over 2 hours daily starting on day 1. ATO will be continued until hematological CR or for a maximum of 60 days. Consolidation ATO, 0.15 mg/Kg IV over 2 hours daily for 5 days every week. Treatment will be continued for 4 weeks on and 4 weeks off, for a total of 4 cycles (last cycle administered on weeks 25 - 28).
Induction Idarubicin, 12 mg/m² on days 2, 4, 6 and 8 by short (20') intravenous infusion . If no hematological CR is achieved by 60 days after start of induction, patient will go off-study. Consolidation 1st cycle Idarubicin, 5 mg/m2/day by short (20') intravenous infusion on days 1, 2, 3, 4. 3rd cycle Idarubicin, 12 mg/m2/day as short (20') intravenous infusion only on day 1.
Event-free survival
As of 14th september 2010, all patients needed to evaluate the primary endpoint have been recruited.
Time frame: At maximum 3.5 years from study entry
Rate of hematological complete remission
Time frame: At maximum 60 days from induction therapy start
Overall survival rate
Time frame: At 2 years from study entry
Rate of cumulative incidence of relapse
Time frame: At 2 years from study entry
Incidence of hematological and non-hematological toxicity episodes during treatment as assessed by CTC-NCI
Time frame: At maximum 60 days from induction therapy start and at maximum 225 days from consolidation therapy start
Rate of molecular remission after 3rd consolidation course
Time frame: At maximum 225 days grom consolidation therapy start
Assessment of acute promyelocytic leukemia/RARa transcript level reduction after induction and during consolidation therapy
Time frame: At maximum 60 days from induction therapy start and at maximum 225 days from consolidation therapy start
Quality of life at the end of induction therapy and at the end of the 3rd consolidation course
Time frame: At maximum 60 days from induction therapy start and at maximum 225 days from consolidation therapy start
Event free survival
Time frame: At 2 years from study entry
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Maintenance therapy 6-Mercaptopurine (6-MP), 50 mg/m2/day orally. The dose will be adjusted according to hematopoietic toxicity during the follow-up period
Maintenance therapy Methotrexate (MTX), 15 mg/m2/weekly intramuscularly. The dose will be adjusted according to toxicity during the follow-up period.
Induction ATRA, 45 mg/m²/day will be administered orally in two equally divided doses and rounded to the nearest 10 mg increment, starting on day 1. ATRA treatment will be continued until hematological CR and for a maximum of 60 days. Consolidation 1. st cycle ATRA, 45 mg/m2/day, will be administered orally in two equally divided doses and rounded to the nearest 10 mg increment, starting from day 1 to day 15. 2. nd cycle ATRA, 45 mg/m2/day will be administered orally in two equally divided doses and rounded to the nearest 10 mg increment, starting from day 1 to day 15. 3. rd cycle ATRA, 45 mg/m2/day will be administered orally in two equally divided doses and rounded to the nearest 10 mg increment, starting from day 1 to day 15. Maintenance therapy ATRA, 45 mg/m2/day orally, for 15 days every three months until a two year period is completed.
Induction All-trans retinoic acid (ATRA), 45 mg/m²/day will be administered orally in two equally divided doses and rounded to the nearest 10 mg increment, starting on day 1. ATRA treatment will be continued until hematological complete remission (CR, see below for definition) or for a maximum of 60 days. Consolidation ATRA, 45 mg/m²/day will be administered orally in two equally divided doses and rounded to the nearest 10 mg increment. Treatment will be administered for 2 weeks on 2 weeks off and for a total of 7 cycles (last cycle administered on weeks 25 - 26).
Universitätsklinik Innsbruck Hämatologie Onkologie
Innsbruck, Austria
Krankenhaus der Barmherzigen Schwestern Linz
Linz, Austria
Universitätsklinik für Innere Medizin III Salzburg
Salzburg, Austria
Klinikum Bayreuth GmbH
Bayreuth, Germany
Charité Campus Benjamin Franklin Berlin
Berlin, Germany
Städt. Kliniken Bielefeld gem. GmbH
Bielefeld, Germany
Universitätsklinikum Bonn
Bonn, Germany
Ev. Diakonie-Krankenhaus gGmbH Bremen
Bremen, Germany
Klinikum Bremen-Mitte gGmbH
Bremen, Germany
Klinikum Chemnitz gGmbH
Chemnitz, Germany
...and 100 more locations
Total hospitalization days during study therapy
Time frame: At maximum 3.5 years from study entry
Event-free survival rate in the two arms
Time frame: At 2 years from study entry