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Secondary genetic lesions in acute myeloid leukemia with inv(16) or t(16;16): a study of the German-Austrian AML Study Group (AMLSG)‏ by Peter Paschka,

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Presentation on theme: "Secondary genetic lesions in acute myeloid leukemia with inv(16) or t(16;16): a study of the German-Austrian AML Study Group (AMLSG)‏ by Peter Paschka,"— Presentation transcript:

1 Secondary genetic lesions in acute myeloid leukemia with inv(16) or t(16;16): a study of the German-Austrian AML Study Group (AMLSG)‏ by Peter Paschka, Juan Du, Richard F. Schlenk, Verena I. Gaidzik, Lars Bullinger, Andrea Corbacioglu, Daniela Späth, Sabine Kayser, Brigitte Schlegelberger, Jürgen Krauter, Arnold Ganser, Claus-Henning Köhne, Gerhard Held, Marie von Lilienfeld- Toal, Heinz Kirchen, Mathias Rummel, Katharina Götze, Heinz-August Horst, Mark Ringhoffer, Michael Lübbert, Mohammed Wattad, Helmut R. Salih, Andrea Kündgen, Hartmut Döhner, and Konstanze Döhner Blood Volume 121(1): January 3, 2013 ©2013 by American Society of Hematology

2 Pie chart illustrating the genetic heterogeneity and coexistence of the distinct secondary genetic abnormalities in AML with inv (16). Paschka P et al. Blood 2013;121: ©2013 by American Society of Hematology

3 Impact of trisomy 22 on RFS and OS. (A) RFS. (B) OS. Paschka P et al. Blood 2013;121: ©2013 by American Society of Hematology

4 Impact of trisomy 8 on OS. Paschka P et al. Blood 2013;121: ©2013 by American Society of Hematology

5 Impact of KIT mutations on RFS. Paschka P et al. Blood 2013;121: ©2013 by American Society of Hematology

6 Impact of FLT3 mutations on OS. Paschka P et al. Blood 2013;121: ©2013 by American Society of Hematology


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