Kolb Michelle, Offer Katharine, Jin Zhezhen, Kahn Justine, Bhatia Monica, Kung Andrew L, Garvin James H, George Diane, Satwani Prakash
Department of Nursing, New York-Presbyterian Morgan Stanley Children's Hospital, New York, New York.
Department of Pediatrics, Columbia University, New York, New York.
Biol Blood Marrow Transplant. 2016 May;22(5):957-61. doi: 10.1016/j.bbmt.2016.02.005. Epub 2016 Feb 13.
Tacrolimus (FK506) is a calcineurin inhibitor and is an essential component of many immunosuppressive regimens. The oral bioavailability of tacrolimus may be affected by many factors, including patient age and gender, as well as by drug-drug interactions or genetic polymorphisms in drug metabolism. The dosing recommendations for pediatric allogeneic hematopoietic cell transplantation (alloHCT) recipients have been derived from tacrolimus use in adult solid-organ transplantation patients. Data describing the impact of conversion of i.v. tacrolimus to oral on the incidence of acute graft-versus-host disease (aGVHD) are limited in children after alloHCT. In this study, we describe the incidence of grades II to IV aGVHD after conversion from i.v. tacrolimus to oral tacrolimus and study the clinical factors associated with delayed achievement of therapeutic blood levels. In this retrospective analysis, 68 pediatric patients (median age, 6.7 years; range, .25 to 22 years), underwent alloHCT for malignant and nonmalignant diseases and received tacrolimus and mycophenolate mofetil for aGVHD prophylaxis. Among all patients, the median number of days to achieve therapeutic tacrolimus trough concentration (10 ng/mL to 20 ng/mL) was 7 days (range, 0 to 37 days). Twenty-two patients developed grades II to IV aGVHD and the cumulative incidence of grades II to IV aGVHD in all patients was 32.4% (standard error, .06). On multivariate analysis ethnicity (white versus others: odds ratio [OR], -4.5; 95% confidence interval [95% CI], 1.091 to 18.91; P = .038) and ≥ 10 days of subtherapeutic tacrolimus levels in first 30 days on i.v. (OR, -3.8; 95% CI, 1.276 to 11.43; P = .017) were significantly associated with delay in achieving therapeutic tacrolimus trough concentration. The impact of race/ethnicity on therapeutic tacrolimus trough concentration in pediatric alloHCT recipients should be further studied prospectively so that individualized dosing plans can be developed.
他克莫司(FK506)是一种钙调神经磷酸酶抑制剂,是许多免疫抑制方案的重要组成部分。他克莫司的口服生物利用度可能受到多种因素影响,包括患者年龄和性别,以及药物相互作用或药物代谢中的基因多态性。儿科异基因造血细胞移植(alloHCT)受者的给药建议源自他克莫司在成人实体器官移植患者中的使用情况。关于异基因造血细胞移植后儿童患者中静脉注射他克莫司转换为口服给药对急性移植物抗宿主病(aGVHD)发生率影响的数据有限。在本研究中,我们描述了从静脉注射他克莫司转换为口服他克莫司后II至IV级aGVHD的发生率,并研究与治疗性血药浓度延迟达到相关的临床因素。在这项回顾性分析中,68例儿科患者(中位年龄6.7岁;范围0.25至22岁)因恶性和非恶性疾病接受了异基因造血细胞移植,并接受他克莫司和霉酚酸酯预防aGVHD。在所有患者中,达到治疗性他克莫司谷浓度(10 ng/mL至20 ng/mL)的中位天数为7天(范围0至37天)。22例患者发生了II至IV级aGVHD,所有患者中II至IV级aGVHD的累积发生率为32.4%(标准误0.06)。多因素分析显示,种族(白人相对于其他种族:比值比[OR],-4.5;95%置信区间[95%CI],1.091至18.91;P = 0.038)以及静脉注射后前30天内他克莫司血药浓度低于治疗水平≥10天(OR,-3.8;95%CI,1.276至11.43;P = 0.017)与达到治疗性他克莫司谷浓度延迟显著相关。种族/民族对儿科异基因造血细胞移植受者治疗性他克莫司谷浓度的影响应进一步进行前瞻性研究,以便制定个体化给药方案。