作者: W. Plunkett , V. Heinemann , E. Estey , M. Keating
DOI: 10.1007/978-3-642-74643-7_111
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摘要: The ability to accumulate and retain the active metabolite of Ara-C varies widely among patients. Our studies demonstrate a significant correlation between clinical response pharmacokinetics Ara-CTP in leukemia cells during therapy. Knowledge cellular pharmacology has been used optimize dose rates design combination treatment schedules. An understanding pharmacodynamics other drugs is likely be useful parameter for planning protocols.