Maruyama Takumi, Kasai Hidefumi, Fukaya Yutaka, Shiokawa Mitsuru, Kimura Toshimi, Hamada Yukihiro
Department of Pharmacy, Tokyo Women's Medical University Hospital, Tokyo, Japan.
Department of Pharmacy, Kochi Medical School Hospital, Kochi, Japan.
Front Microbiol. 2024 Oct 8;15:1480874. doi: 10.3389/fmicb.2024.1480874. eCollection 2024.
Letermovir (LET) is a novel antiviral agent recently approved for cytomegalovirus (CMV) prophylaxis of renal transplant patients in Japan. However, its interactions with tacrolimus (TAC), an important immunosuppressant, remain ambiguous, warranting careful evaluation considering the unique genetic and physiological characteristics of Japanese patients. Therefore, in this study, we aimed to investigate the drug-drug interactions between LET and extended-release TAC (ER-TAC) in Japanese renal transplant patients via physiologically based pharmacokinetic (PBPK) modeling. We developed PBPK models for LET and TAC, including a new model for ER-TAC, using the Simcyp simulator. We also created a virtual Japanese post-transplant population by incorporating physiological parameters specific to Japanese patients, including CYP3A5 genotypes. Our model accurately predicted the pharmacokinetics of both immediate-release and ER-TAC co-administered with LET. In the Japanese population, LET significantly increased ER-TAC exposure, with the effect varying by CYP3A5 genotype. For carrier, the area under the curve ratio ranged from 2.33 to 2.53, while for carriers, it ranged from 2.82 to 2.86. The maximum concentration ratio was approximately 1.50 across all groups. Our findings suggest reducing the ER-TAC dose by approximately 57-60% for carrier and 65% for carriers when co-administered with LET for Japanese renal transplant patients. Moreover, the developed model incorporating population-specific factors, such as hematocrit values and CYP3A5 genotype frequencies, is a valuable tool to evaluate complex drug interactions and guide the dosing strategies for LET and TAC in Japanese patients. Overall, this study expands the application of PBPK modeling in transplant pharmacology, contributing to the development of effective immunosuppressive strategies for Japanese renal transplant patients.
来特莫韦(LET)是一种新型抗病毒药物,最近在日本被批准用于肾移植患者的巨细胞病毒(CMV)预防。然而,它与重要的免疫抑制剂他克莫司(TAC)之间的相互作用仍不明确,鉴于日本患者独特的遗传和生理特征,有必要进行仔细评估。因此,在本研究中,我们旨在通过基于生理的药代动力学(PBPK)模型研究日本肾移植患者中LET与缓释TAC(ER-TAC)之间的药物相互作用。我们使用Simcyp模拟器开发了LET和TAC的PBPK模型,包括一个新的ER-TAC模型。我们还通过纳入日本患者特有的生理参数,包括CYP3A5基因型,创建了一个虚拟的日本移植后人群。我们的模型准确预测了与LET联合给药的速释和ER-TAC的药代动力学。在日本人群中,LET显著增加了ER-TAC的暴露量,其效果因CYP3A5基因型而异。对于携带者,曲线下面积比在2.33至2.53之间,而对于携带者,其范围在2.82至2.86之间。所有组的最大浓度比约为1.50。我们的研究结果表明,对于日本肾移植患者,当与LET联合使用时,携带者的ER-TAC剂量应减少约57-60%,携带者应减少65%。此外,所开发的纳入特定人群因素(如血细胞比容值和CYP3A5基因型频率)的模型是评估复杂药物相互作用并指导日本患者LET和TAC给药策略的有价值工具。总体而言,本研究扩展了PBPK模型在移植药理学中的应用,有助于为日本肾移植患者制定有效的免疫抑制策略。