Mulder M B, Busschbach J J, van Hoek B, Polak W G, Alwayn I P J, de Winter B C M, Murad S Darwish, Verhey-Hart E, Elshove L, Erler N S, Hesselink D A, den Hoed C M, Metselaar H J
Department of Hospital Pharmacy, Erasmus MC, University Medical Center Rotterdam, Rotterdam, Netherlands.
Erasmus MC Transplant Institute, Rotterdam, Netherlands.
Transpl Int. 2025 Apr 28;38:14189. doi: 10.3389/ti.2025.14189. eCollection 2025.
We investigated whether life cycle pharma (LCP)-tacrolimus compared to extended-release (ER)-tacrolimus results in a difference in severity of tremors and HRQoL. In this multi-center, open-label, randomized, controlled trial, 108 patients were randomized in a 1:1 ratio to either LCP-tacrolimus regimen or ER-tacrolimus regimen after transplantation. HRQoL was assessed with the EQ-5D-5L and SF-36 questionnaire (two generic HRQoL instruments) and the quality of life in essential tremor (QUEST) questionnaire (domain specific HRQoL instrument). The EQ-5D-5L scores were translated to the societal values. We examined the HRQoL over the course of the study by fitting generalized mixed effect models. In total, 105 patients were included, 53 to the LCP- and 52 to the ER-tacrolimus regimen. Baseline questionnaires were available for every LT recipient. At 12 months 25% [10/40], 95% confidence interval (CI) 14.2%-40.2% of the LT recipients in the LCP-tacrolimus regimen group experienced tremors compared to 30.4% [14/46], 95%-CI 19.1%-44.8% of the LT recipients in the ER-tacrolimus regimen group; risk difference: 0.054; 95%-CI -0.151-0.249; p = 0.63. No statistically significant differences in HRQoL were seen between the two regimens. We could not demonstrate differences in the HRQoL or occurrence of tremors between LCP-tacrolimus and ER-tacrolimus regimens.
我们研究了与缓释(ER)他克莫司相比,生命周期制药(LCP)他克莫司在震颤严重程度和健康相关生活质量(HRQoL)方面是否存在差异。在这项多中心、开放标签、随机对照试验中,108例患者在移植后按1:1比例随机分为LCP他克莫司方案组或ER他克莫司方案组。使用EQ-5D-5L和SF-36问卷(两种通用的HRQoL工具)以及特发性震颤生活质量(QUEST)问卷(特定领域的HRQoL工具)评估HRQoL。EQ-5D-5L评分被转换为社会价值。我们通过拟合广义混合效应模型在研究过程中检查HRQoL。总共纳入了105例患者,53例接受LCP他克莫司方案,52例接受ER他克莫司方案。每位肝移植受者都有基线问卷。在12个月时,LCP他克莫司方案组中25%[10/40],95%置信区间(CI)为14.2%-40.2%的肝移植受者出现震颤,而ER他克莫司方案组中为30.4%[14/46],95%-CI为19.1%-44.8%;风险差异:0.054;95%-CI为-0.151-0.249;p = 0.63。两种方案在HRQoL方面未观察到统计学上的显著差异。我们无法证明LCP他克莫司和ER他克莫司方案在HRQoL或震颤发生率方面存在差异。