Abstract
The treatment of adults with ALL, although not offering the same satisfactory long-term disease-free survivals (DFS) as is afforded to the majority of children, has improved steadily over the past decades. Outcomes have improved for all adult age groups except for the over sixties [1]. Treating physicians are very much aware that age has, arguably, the most significant impact on outcome. To what extent that relates to the changing biology of the disease with age, per se, or whether it results from a different approach to – or tolerance of – therapy is unclear.
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Fielding, A.K. (2011). Prognostic Factors in Adult Acute Lymphoblastic Leukemia (ALL). In: Advani, A., Lazarus, H. (eds) Adult Acute Lymphocytic Leukemia. Contemporary Hematology. Humana Press. https://doi.org/10.1007/978-1-60761-707-5_7
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DOI: https://doi.org/10.1007/978-1-60761-707-5_7
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