Arsenic trioxide dose capping to decrease toxicity in the treatment of acute promyelocytic leukemia

被引:8
作者
Zacholski, Kyle [1 ]
Hambley, Bryan [2 ]
Hickey, Erin [3 ]
Kashanian, Sarah [4 ]
Li, Andrew [4 ]
Baer, Maria R. [4 ,5 ]
Duong, Vu H. [4 ,5 ]
Newman, Matthew J. [1 ]
DeZern, Amy [2 ]
Gojo, Ivana [2 ]
Smith, B. Douglas [2 ]
Levis, Mark J. [2 ]
Varadhan, Ravi [2 ]
Gehrie, Eric [6 ]
Emadi, Ashkan [4 ,5 ]
Ghiaur, Gabriel [2 ]
机构
[1] Johns Hopkins Univ Hosp, Sidney Kimmel Comprehens Canc Ctr, Dept Pharm, Baltimore, MD 21287 USA
[2] Johns Hopkins Univ, Sch Med, Sidney Kimmel Comprehens Canc Ctr, Baltimore, MD USA
[3] Virginia Commonwealth Univ, Sch Pharm, Richmond, VA USA
[4] Univ Maryland, Sch Med, Baltimore, MD 21201 USA
[5] Univ Maryland, Greenebaum Comprehens Canc Ctr, Baltimore, MD 21201 USA
[6] Johns Hopkins Univ, Dept Pathol, Transfus Med Div, Baltimore, MD USA
基金
美国国家卫生研究院;
关键词
Acute promyelocytic leukemia; arsenic trioxide; obesity; toxicity; capped dose; RETINOIC ACID; RISK; CHEMOTHERAPY; CHILDREN; OBESITY;
D O I
10.1177/10781552211024727
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Arsenic trioxide (ATO) and all-trans retinoic acid (ATRA) combination therapy yields high complete remission and disease-free survival rates in acute promyelocytic leukemia (APL). ATO is dosed on actual body weight and high ATO doses in overweight patients may contribute to increased toxicity. We performed a retrospective, two-center study comparing toxicities in patients who received the Lo-Coco et al ATRA/ATO regimen with capped ATO, <= 10 mg/dose, and non-capped ATO, >10 mg/dose. A total of 44 patients were included; 15 received doses <= 10 mg and 29 received >10 mg. During induction, there was no difference in the incidence of grade >= 3 hepatotoxicity, grade >= 3 QTc prolongation, neurotoxicity, and cardiac toxicity between groups. In consolidation, patients receiving >10 mg/dose experienced a greater incidence of neurotoxicity (66.7% vs 22.2%; p = 0.046). Capping doses saved $24634.37/patient and reduced waste of partially-used vials. At a median follow-up of 27 months, no disease relapses occurred in either group. This represents an opportunity to improve the safety profile of this highly effective regimen.
引用
收藏
页码:1340 / 1349
页数:10
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