在儿科急性髓性白血病中药物基因组学,种族和治疗结果

Jatinder K Lamba1,2,3, Richard Marrero1, Huiyun Wu4

  • 1Department of Pharmacotherapy and Translational Research, College of Pharmacy, University of Florida, Gainesville.

JAMA network open
|May 16, 2024
PubMed
概括

增强诱导疗法消除了黑人患者急性髓性白血病 (AML) 结果中的种族差异. 使用药物基因组学量身定制治疗可能会进一步缩小AML存活率的差距.

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