Zusammenfassung
Dank genetischer und molekularer Techniken wurden zunehmende Einblicke in die Biologie der akuten myeloischen Leukämie (AML) gewonnen. Neuere Erkenntnisse zeigen, dass es sich bei der AML nicht um eine homogene Krankheitsentität, sondern um eine heterogene Gruppe biologisch unterschiedlicher Subtypen handelt. Diese Untergruppen werden derzeit überwiegend über zytogenetische und molekulare Marker definiert. Klinisch weisen sie ausgeprägte Unterschiede im Ansprechen auf Therapie und Langzeitergebnisse auf und erlauben daher die Definition von Risikogruppen. Solche Risikogruppen werden in Zukunft Grundlage therapeutischer Entscheidungen sein und letztlich zu einer individualisierten Therapiestrategie führen.
Abstract
Genetic and molecular techniques have provided increasing insights into the biology of acute myeloid leukemia (AML). These investigations showed that AML is not a homogeneous disease but a heterogeneous group of biologically different subentities. These subentities are currently primarily defined by cytogenetics and molecular markers. They differ substantially in response to therapy and long-term outcome and hence allow different risk groups of patients to be defined. These will guide therapeutic decisions in future therapeutic strategies and may ultimately lead to an individualized treatment concept.
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Hiddemann, W., Spiekermann, K., Braess, J. et al. Risikoadaptierte Therapie der akuten myeloischen Leukämie. Internist 47 (Suppl 1), S33–S39 (2006). https://doi.org/10.1007/s00108-006-1622-y
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DOI: https://doi.org/10.1007/s00108-006-1622-y