Abstract
About 20–25% of adult patients with acute lymphoblastic leukemia (ALL) present with a Philadelphia chromosome t(9;22) as cytogenetic marker and/or on a molecular level with the corresponding BCR-ABLrearrangement [1–4]. The proportion of ALL-patients with Ph+/BCR-ABL+ ALL increases with age. The median age of patients with BCR-ABL+ ALL in the German multicenter adult ALL (GMALL) trials is 45 years [4].
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Martin, H., Goekburget, N., Atta, J., Ludwig, WD., Hoelzer, D. (1998). Treatment of Ph+ and t(4;11)+ Acute Lymphoblastic Leukemia in Adults. In: Hiddemann, W., et al. Acute Leukemias VII. Haematology and Blood Transfusion / Hämatologie und Bluttransfusion, vol 39. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-71960-8_103
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DOI: https://doi.org/10.1007/978-3-642-71960-8_103
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