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    Klinische Pädiatrie. 2015 May 18. doi: 10.1055/s-0035-1548816
    Randomised Introduction of 2-CDA as Intensification during Consolidation for Children with High-risk AML--results from Study AML-BFM 2004.
    Creutzig U1,  Dworzak M2,  Zimmermann M3,  Bourquin JP4,  Gruhn B5,  Fleischhack G6,  Graf N7,  Klingebiel T8,  Kremens B9,  Lehrnbecher T10,  von Neuhoff C11,  von Stackelberg A12,  Stray J13,  Reinhardt D14
    Author information
    1Department of Pediatric Hematology and Oncology, Children's Hospital, Hannover Medical School, Hannover, Germany.
    2St. Anna Children's Hospital and Children's Cancer Research Institute, Department of Pediatrics, Medical University of Vienna, Vienna, Austria.
    3Department of Pediatric Hematology and Oncology, Children's Hospital, Hannover Medical School, Hannover, Germany.
    4Pediatric Hematology/Oncology, Zürich, University of Zurich, Switzerland.
    5Department of Pediatrics, Jena University Hospital, Jena, Germany.
    6Paediatric Hematology and Oncology, Medical Center, University of Essen, Essen, Germany.
    7Paediatric Haematology and Oncology, Children's Hospital Medical Center, Homburg, Germany.
    8Pediatric Hematology, Oncology and Hemostaseology, University Children's Hospital of Frankfurt/Main, Goethe-University Frankfurt/Main, Frankfurt, Germany.
    9Paediatric Hematology and Oncology, Medical Center, University of Essen, Essen, Germany.
    10Pediatric Hematology, Oncology and Hemostaseology, University Children's Hospital of Frankfurt/Main, Goethe-University Frankfurt/Main, Frankfurt, Germany.
    11Paediatric Hematology and Oncology, Medical Center, University of Essen, Essen, Germany.
    12Department of Pediatric Oncology/Hematology, Charité Universitätsmedizin Berlin, Berlin, Germany.
    13Department of Pediatric Hematology and Oncology, 2nd Faculty of Medicine, Charles University and University Hospital Motol, Prague, Czech Republic.
    14Paediatric Hematology and Oncology, Medical Center, University of Essen, Essen, Germany.
    Abstract

    BACKGROUND: The outcome in children and adolescents with high-risk (HR) acute myeloid leukemia (AML) is still unsatisfactory. Therefore, in study AML-BFM 2004 we aimed to improve outcome of HR-patients by adding moderately dosed 2-Chloro-2-Deoxyadenosine (2-CDA) to the respective consolidation treatment backbone without increasing toxicity. The aim was to improve prognosis especially in FAB M4/M5/MLL patients, who represent the largest subgroup of HR patients.

    PATIENTS AND METHODS: In total, 343 children and adolescents with HR-AML were randomized to receive or not 2-CDA (6 mg/m²/d, days 1, 3) in combination with cytarabine/idarubicine (AI=500 mg/m² cytarabine 5 days continuous infusion plus 7 mg/m²/d idarubicin, days 3 and 5).

    RESULTS: RESULTS for patients of the AI/2-CDA arm (n=168) vs. the AI-arm (n=175) were similar: 5-year overall survival 68±4 vs. 72±4%, plogrank=0.38, event-free survival 53±4 vs. 49±4%, plogrank=0.77; cumulative incidence of relapse at 5 years: 35±4 vs. 37±4%, p(Gray)=0.89. RESULTS in patients with MLL rearrangement or FAB M4/M5 were also similar in the treatment groups. In addition, toxicities did not differ between the two arms.

    CONCLUSION: We conclude that additional, moderate dose 2-CDA does not improve prognosis in HR-patients when given during consolidation treatment. Its effect might be too low in this multidrug regimen, where the strongest effects are achieved during induction, or the chosen dose of 2-CDA might have been too low.


    © Georg Thieme Verlag KG Stuttgart · New York.

    Publikations ID: 25985446
    Quelle: öffnen
     
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