Khong Jeffrey, Lee Megan, Warren Curtis, Kim Un Bi, Duarte Sergio, Andreoni Kenneth A, Shrestha Sunaina, Johnson Mark W, Battula Narendra R, McKimmy Danielle M, Beduschi Thiago, Lee Ji-Hyun, Li Derek M, Ho Chih-Ming, Zarrinpar Ali
medRxiv. 2023 Jun 3:2023.05.26.23290604. doi: 10.1101/2023.05.26.23290604.
Inter- and intra-individual variability in tacrolimus dose requirements mandates empirical clinician-titrated dosing that frequently results in deviation from a narrow target range. Improved methods to individually dose tacrolimus are needed. Our objective was to determine whether a quantitative, dynamically-customized, phenotypic-outcome-guided dosing method termed Phenotypic Personalized Medicine (PPM) would improve target drug trough maintenance.
In a single-center, randomized, pragmatic clinical trial ( NCT03527238 ), 62 adults were screened, enrolled, and randomized prior to liver transplantation 1:1 to standard-of-care (SOC) clinician-determined or PPM-guided dosing of tacrolimus. The primary outcome measure was percent days with large (>2 ng/mL) deviation from target range from transplant to discharge. Secondary outcomes included percent days outside-of-target-range and mean area-under-the-curve (AUC) outside-of-target-range per day. Safety measures included rejection, graft failure, death, infection, nephrotoxicity, or neurotoxicity.
56 (29 SOC, 27 PPM) patients completed the study. The primary outcome measure was found to be significantly different between the two groups. Patients in the SOC group had a mean of 38.4% of post-transplant days with large deviations from target range; the PPM group had 24.3% of post-transplant days with large deviations; (difference -14.1%, 95% CI: -26.7 to -1.5 %, P=0.029). No significant differences were found in the secondary outcomes. In post-hoc analysis, the SOC group had a 50% longer median length-of-stay than the PPM group [15 days (Q1-Q3: 11-20) versus 10 days (Q1-Q3: 8.5-12); difference 5 days, 95% CI: 2-8 days, P=0.0026].
PPM guided tacrolimus dosing leads to better drug level maintenance than SOC. The PPM approach leads to actionable dosing recommendations on a day-to-day basis.
In a study on 62 adults who underwent liver transplantation, researchers investigated whether a new dosing method called Phenotypic Personalized Medicine (PPM) would improve daily dosing of the immunosuppression drug tacrolimus. They found that PPM guided tacrolimus dosing leads to better drug level maintenance than the standard-of-care clinician-determined dosing. This means that the PPM approach leads to actionable dosing recommendations on a day-to-day basis and can help improve patient outcomes.
他克莫司剂量需求存在个体间和个体内差异,这就要求临床医生根据经验进行滴定给药,而这常常导致偏离狭窄的目标范围。因此需要改进他克莫司的个体化给药方法。我们的目的是确定一种定量的、动态定制的、表型结果导向的给药方法——表型个性化医学(PPM)是否能改善目标药物谷浓度的维持。
在一项单中心、随机、实用的临床试验(NCT03527238)中,62名成年人在肝移植前接受筛选、入组,并按1:1随机分为他克莫司标准治疗(SOC)临床医生确定给药组或PPM指导给药组。主要结局指标是从移植到出院时与目标范围有较大偏差(>2 ng/mL)的天数百分比。次要结局包括超出目标范围的天数百分比以及每天超出目标范围的平均曲线下面积(AUC)。安全指标包括排斥反应、移植物功能衰竭、死亡、感染、肾毒性或神经毒性。
56名(29名SOC组,27名PPM组)患者完成了研究。发现两组的主要结局指标存在显著差异。SOC组患者移植后有较大偏差天数的平均比例为38.4%;PPM组为24.3%;(差异为-14.1%,95%CI:-26.7至-1.5%,P = 0.029)。次要结局未发现显著差异。事后分析中,SOC组的中位住院时间比PPM组长50%[15天(Q1-Q3:11-20)对10天(Q1-Q3:8.5-12);差异5天,95%CI:2-8天,P = 0.0026]。
PPM指导的他克莫司给药比SOC能更好地维持药物水平。PPM方法能在日常基础上给出可操作的给药建议。
在一项针对62名接受肝移植的成年人的研究中,研究人员调查了一种名为表型个性化医学(PPM)的新给药方法是否能改善免疫抑制药物他克莫司的每日给药。他们发现,PPM指导的他克莫司给药比标准治疗临床医生确定的给药能更好地维持药物水平。这意味着PPM方法能在日常基础上给出可操作的给药建议,并有助于改善患者预后。