Dai Zi-Yan, Han Lu, Wang Juan, Liu Xiao-Qin, Chen Rui, Jiao Zheng
Department of Pharmacy, Shanghai Chest Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
School of Pharmacy, Shanghai Jiao Tong University, Shanghai, China.
J Clin Pharmacol. 2025 Aug;65(8):980-987. doi: 10.1002/jcph.70021. Epub 2025 Mar 27.
Tacrolimus, a critical immunosuppressant in organ transplantation, is available in immediate-release (IR-T) and extended-release (ER-T) formulations. While ER-T improves patient adherence, clinical studies have not demonstrated superior outcomes compared to IR-T. However, the underlying reasons for this discrepancy remain unclear. This study aimed to evaluate tacrolimus exposure under non-adherent dosing behaviors with IR-T and ER-T and to provide insights for selecting the optimal tacrolimus formulation. Monte Carlo simulations were conducted to assess the proportion of target attainment (%PTA) and deviation time (DT) from the therapeutic range in scenarios involving delayed or missed doses, based on published population pharmacokinetic models. The influence of renal function, the post-transplantation period, and hematocrit levels on %PTA and DT were also analyzed. Our findings revealed that patients on ER-T exhibited lower %PTA and longer DT than those on IR-T when doses were delayed or missed, reflecting poorer "forgiveness." This observation elucidates the lack of clinical superiority observed for ER-T in previous studies. Furthermore, fast metabolizers experienced worse forgiveness with ER-T, exacerbating the challenge of maintaining therapeutic levels. Additionally, a web-based dashboard was developed to calculate the %PTA and DT for individual patients and to provide formulation recommendations tailored to their dosing behaviors and clinical characteristics. In conclusion, adherence and forgiveness play a crucial role in the success of pharmacotherapy. This study highlights the significance of pharmacokinetic modeling and simulation in providing evidence-based recommendations for selecting the optimal tacrolimus formulation.
他克莫司是器官移植中一种关键的免疫抑制剂,有速释(IR-T)和缓释(ER-T)两种剂型。虽然ER-T可提高患者的依从性,但临床研究并未证明其疗效优于IR-T。然而,这种差异的潜在原因仍不清楚。本研究旨在评估IR-T和ER-T在非依从性给药行为下的他克莫司暴露情况,并为选择最佳他克莫司剂型提供见解。基于已发表的群体药代动力学模型,进行蒙特卡洛模拟,以评估在涉及延迟或漏服剂量的情况下达到目标的比例(%PTA)和偏离治疗范围的时间(DT)。还分析了肾功能、移植后时期和血细胞比容水平对%PTA和DT的影响。我们的研究结果显示,当剂量延迟或漏服时,服用ER-T的患者的%PTA较低,DT较长,这反映出其“宽容度”较差。这一观察结果解释了先前研究中未观察到ER-T具有临床优势的原因。此外,快速代谢者使用ER-T时的宽容度更差,这加剧了维持治疗水平的挑战。此外,还开发了一个基于网络的仪表盘,用于计算个体患者的%PTA和DT,并根据其给药行为和临床特征提供剂型推荐。总之,依从性和宽容度在药物治疗的成功中起着关键作用。本研究强调了药代动力学建模和模拟在为选择最佳他克莫司剂型提供循证推荐方面的重要性。