Endogenous thrombopoietin serum levels during multicycle chemotherapy
Christoph Engel
Institute for Medical Informatics, Statistics and Epidemiology, University of Leipzig, Leipzig,
Search for more papers by this authorMarkus Loeffler
Institute for Medical Informatics, Statistics and Epidemiology, University of Leipzig, Leipzig,
Search for more papers by this authorHorst Franke
Institute for Medical Informatics, Statistics and Epidemiology, University of Leipzig, Leipzig,
Search for more papers by this authorStephan Schmitz
Department I for Internal Medicine, University of Cologne, Cologne, Germany
Search for more papers by this authorChristoph Engel
Institute for Medical Informatics, Statistics and Epidemiology, University of Leipzig, Leipzig,
Search for more papers by this authorMarkus Loeffler
Institute for Medical Informatics, Statistics and Epidemiology, University of Leipzig, Leipzig,
Search for more papers by this authorHorst Franke
Institute for Medical Informatics, Statistics and Epidemiology, University of Leipzig, Leipzig,
Search for more papers by this authorStephan Schmitz
Department I for Internal Medicine, University of Cologne, Cologne, Germany
Search for more papers by this authorAbstract
Little is known about the behaviour of endogenous thrombopoietin (TPO) serum levels during rapid sequences of dose-intensified chemotherapy. To characterize the relationship between TPO levels and platelet counts in this setting we serially measured both parameters over the entire treatment period of patients receiving multicycle polychemotherapy. We found TPO and platelet responses to be generally antagonistic through all cycles. However, a cross-correlation analysis indicated that TPO responses preceded platelet responses by approximately one day in all patients. The cumulative severity of thrombocytopenia observed over successive cycles was accompanied by an increasing TPO response which tended to grow overproportionally in relation to the degree of peripheral thrombocytopenia. These findings are consistent with a model suggesting that both platelet and megakaryocyte mass contribute to a receptor-dependent consumption process regulating the endogenous TPO level. In order to develop optimal schedules for exogenous TPO administration it might be important to consider endogenous TPO response characteristics.
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