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Improved Treatment Results in the Myelocytic Subtypes FAB M1-M4 but not in FAB M5 After Intensification of Induction Therapy: Results of the German Childhood AML Studies BFM-78 and BFM-83

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Acute Leukemias II

Part of the book series: Haematology and Blood Transfusion / Hämatologie und Bluttransfusion ((HAEMATOLOGY,volume 33))

Abstract

Acute myelogenous leukemia (AML) represents a heterogeneous group of leukemias. It is a rare disease in children, accounting for approximately 20% of acute leukemia in children and adolescents [10]. In contrast to the major advances in childhood lymphoblastic leukemia (ALL), the progress achieved in childhood AML has been less satisfactory. Approximately 20%–25% of children with AML fail to achieve complete remission and a significant number of children in remission still relapse in spite of postremission treatment with polychemotherapy. Since 1978 the German BFM Group conducted three consecutive studies for the treatment of childhood AML, in which 33 hospitals participated [3, 10, 12]. This report updates the latest results of the first two studies BFM-78 and BFM-83 with special emphasis on the main differences between them.

Supported by the Federal Minister for Research and Technology, Federal Republic of Germany

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© 1990 Springer-Verlag Berlin Heidelberg

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Ritter, J., Creutzig, U., Schellong, G. (1990). Improved Treatment Results in the Myelocytic Subtypes FAB M1-M4 but not in FAB M5 After Intensification of Induction Therapy: Results of the German Childhood AML Studies BFM-78 and BFM-83. In: Büchner, T., Schellong, G., Hiddemann, W., Ritter, J. (eds) Acute Leukemias II. Haematology and Blood Transfusion / Hämatologie und Bluttransfusion, vol 33. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-74643-7_35

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  • DOI: https://doi.org/10.1007/978-3-642-74643-7_35

  • Publisher Name: Springer, Berlin, Heidelberg

  • Print ISBN: 978-3-540-50984-4

  • Online ISBN: 978-3-642-74643-7

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