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MDS and Secondary AML : An Evolutionary Perspective

  • M. William Audeh
Part of the Cancer Treatment and Research book series (CTAR, volume 108)

Abstract

The way in which medicine explains disease determines, to a great extent, the approach that is taken to treatment and prevention ([Thagard, 1999]). Myelodysplastic Syndrome (MDS) and its frequent sequela, secondary Acute Myeloid Leukemia (AML), have been explained as clonal disorders of hematopoietic stem cells, which arise as the result of exposure to genotoxic agents, particularly cancer therapies such as chemotherapy and radiation ([Lichtman and Brennan, 2001]). Treatment has until recently been guided by viewing MDS as a disorder of differentiation, or an incipient malignancy requiring additional genotoxic agents to suppress. These assumptions regarding etiology and therapy may be inadequate to answer fundamental questions regarding this disease, such as why only certain individuals exposed to the same chemotherapeutic agents develop MDS/secondary AML, why certain individuals evolve from MDS to secondary AML more rapidly than others, and why treatment with additional genotoxic agents has not proven curative.

Keywords

Acute Myeloid Leukemia Myelodysplastic Syndrome Acute Myelogenous Leukemia Microsatellite Instability Genetic Instability 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

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Copyright information

© Springer Science+Business Media New York 2001

Authors and Affiliations

  • M. William Audeh
    • 1
    • 2
  1. 1.University of CaliforniaLos Angeles
  2. 2.Division of Hematology/OncologyCedars-Sinai Medical CenterLos Angeles

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