Evaluating risk factors for acute graft versus host disease in pediatric hematopoietic stem cell transplant patients receiving tacrolimus

被引:6
作者
Phan, Michael [1 ]
Chavan, Rishikesh [2 ]
Beuttler, Richard [3 ]
Benipayo, Nicole [4 ]
Magedman, Grace [5 ]
Buchbinder, David [2 ]
Tomaszewski, Daniel [3 ]
Yang, Sun [1 ]
机构
[1] Chapman Univ, Sch Pharm, Dept Pharm Practice, Harry & Diane Rinker Hlth Sci Campus,9401 Jeronim, Irvine, CA 92618 USA
[2] CHOC Childrens Hosp, Hyundai Canc Inst, Orange, CA USA
[3] Chapman Univ, Sch Pharm, Dept Biomed & Pharmaceut Sci, Irvine, CA USA
[4] Chapman Univ, Sch Pharm, Irvine, CA USA
[5] CHOC Childrens Hosp, Dept Pharm, Orange, CA USA
来源
CTS-CLINICAL AND TRANSLATIONAL SCIENCE | 2021年 / 14卷 / 04期
基金
美国国家卫生研究院;
关键词
BONE-MARROW-TRANSPLANTATION; CLINICAL PHARMACOKINETICS; GVHD PROPHYLAXIS; METHOTREXATE; CHILDREN; DONOR; PHARMACOGENETICS; PREVENTION; INFUSION; MOFETIL;
D O I
10.1111/cts.12982
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
To identify the clinical and pharmacological risk factors associated with tacrolimus pharmacodynamics for acute graft-versus-host disease (aGVHD) in pediatric patients receiving allogeneic hematopoietic stem cell transplantation (HSCT) from a matched related donor. A retrospective cohort single center chart review study was conducted with pediatric patients who received tacrolimus prophylaxis after allogeneic HSCT between January 1, 2017, and December 31, 2019. Potential risk factors were tested separately between aGVHD and non-aGVHD cohorts and were further analyzed in a logistic regression model with backward elimination and a partial least squares discriminant analysis. Thirty-three patient cases were included in our study and 52% (17/33) developed aGVHD while on tacrolimus prophylaxis. When tested independently, donor age and sibling versus parent donor/recipient relation were shown to be statistically significant between aGVHD and non-aGVHD patients (p < 0.005). Pharmacological factors associated with tacrolimus treatment failed to demonstrate a significant impact on patient's risk of aGVHD. Using a best fit logistic regression model that tested all the variables together, donor age was the only significant variable predicting patient's risk of aGVHD (p < 0.01). Donor relationship and donor age were unable to be evaluated separately and are therefore confounding variables. Among pediatric patients receiving allogeneic HSCT, aGVHD risk is significantly decreased by either sibling donor and/or younger donors. Although no conclusions were drawn on the effect of tacrolimus therapy (p = 0.08), results warrant additional research with a larger sample size to evaluate the accuracy of monitoring tacrolimus serum trough levels.
引用
收藏
页码:1303 / 1313
页数:11
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