Division of Clinical Pharmacology and Toxicology, University Hospital, Lausanne, Switzerland.
Clin Pharmacokinet. 2009;48(6):399-418. doi: 10.2165/00003088-200948060-00006.
Valganciclovir and ganciclovir are widely used for the prevention of cytomegalovirus (CMV) infection in solid organ transplant recipients, with a major impact on patients' morbidity and mortality. Oral valganciclovir, the ester prodrug of ganciclovir, has been developed to enhance the oral bioavailability of ganciclovir. It crosses the gastrointestinal barrier through peptide transporters and is then hydrolysed into ganciclovir. This review aims to describe the current knowledge of the pharmacokinetic and pharmacodynamic characteristics of this agent, and to address the issue of therapeutic drug monitoring. Based on currently available literature, ganciclovir pharmacokinetics in adult solid organ transplant recipients receiving oral valganciclovir are characterized by bioavailability of 66 +/- 10% (mean +/- SD), a maximum plasma concentration of 3.1 +/- 0.8 mg/L after a dose of 450 mg and of 6.6 +/- 1.9 mg/L after a dose of 900 mg, a time to reach the maximum plasma concentration of 3.0 +/- 1.0 hours, area under the plasma concentration-time curve values of 29.1 +/- 5.3 mg.h/L and 51.9 +/- 18.3 mg.h/L (after 450 mg and 900 mg, respectively), apparent clearance of 12.4 +/- 3.8 L/h, an elimination half-life of 5.3 +/- 1.5 hours and an apparent terminal volume of distribution of 101 +/- 36 L. The apparent clearance is highly correlated with renal function, hence the dosage needs to be adjusted in proportion to the glomerular filtration rate. Unexplained interpatient variability is limited (18% in apparent clearance and 28% in the apparent central volume of distribution). There is no indication of erratic or limited absorption in given subgroups of patients; however, this may be of concern in patients with severe malabsorption. The in vitro pharmacodynamics of ganciclovir reveal a mean concentration producing 50% inhibition (IC(50)) among CMV clinical strains of 0.7 mg/L (range 0.2-1.9 mg/L). Systemic exposure of ganciclovir appears to be moderately correlated with clinical antiviral activity and haematotoxicity during CMV prophylaxis in high-risk transplant recipients. Low ganciclovir plasma concentrations have been associated with treatment failure and high concentrations with haematotoxicity and neurotoxicity, but no formal therapeutic or toxic ranges have been validated. The pharmacokinetic parameters of ganciclovir after valganciclovir administration (bioavailability, apparent clearance and volume of distribution) are fairly predictable in adult transplant patients, with little interpatient variability beyond the effect of renal function and bodyweight. Thus ganciclovir exposure can probably be controlled with sufficient accuracy by thorough valganciclovir dosage adjustment according to patient characteristics. In addition, the therapeutic margin of ganciclovir is loosely defined. The usefulness of systematic therapeutic drug monitoring in adult transplant patients therefore appears questionable; however, studies are still needed to extend knowledge to particular subgroups of patients or dosage regimens.
缬更昔洛韦和更昔洛韦广泛用于预防实体器官移植受者的巨细胞病毒 (CMV) 感染,对患者的发病率和死亡率有重大影响。更昔洛韦的口服前体药物缬更昔洛韦,旨在提高更昔洛韦的口服生物利用度。它通过肽转运体穿过胃肠道屏障,然后被水解成更昔洛韦。本综述旨在描述该药物的药代动力学和药效学特征,并探讨治疗药物监测的问题。根据目前的文献,口服缬更昔洛韦的成年实体器官移植受者的更昔洛韦药代动力学特征为:生物利用度为 66 +/- 10%(平均值 +/- 标准差),剂量为 450mg 时最大血浆浓度为 3.1 +/- 0.8mg/L,剂量为 900mg 时为 6.6 +/- 1.9mg/L,达到最大血浆浓度的时间为 3.0 +/- 1.0 小时,血浆浓度-时间曲线下面积值分别为 29.1 +/- 5.3mg.h/L 和 51.9 +/- 18.3mg.h/L(分别为 450mg 和 900mg 时),表观清除率为 12.4 +/- 3.8L/h,消除半衰期为 5.3 +/- 1.5 小时,表观终末分布容积为 101 +/- 36L。表观清除率与肾功能高度相关,因此需要根据肾小球滤过率调整剂量。个体间的不可解释变异性有限(表观清除率的 18%和表观中央分布容积的 28%)。在特定的患者亚群中,没有吸收不规则或有限的迹象;然而,在严重吸收不良的患者中,这可能是一个问题。更昔洛韦的体外药效学显示,CMV 临床株的 50%抑制浓度(IC(50))平均为 0.7mg/L(范围为 0.2-1.9mg/L)。在高危移植受者中,CMV 预防期间,系统更昔洛韦暴露量与临床抗病毒活性和血液毒性之间呈中度相关。低更昔洛韦血浆浓度与治疗失败有关,高浓度与血液毒性和神经毒性有关,但尚未验证正式的治疗或毒性范围。在成年移植患者中,缬更昔洛韦给药后的更昔洛韦药代动力学参数(生物利用度、表观清除率和分布容积)相当可预测,除了肾功能和体重的影响外,个体间的变异性很小。因此,通过根据患者特征进行充分的缬更昔洛韦剂量调整,可能可以更准确地控制更昔洛韦的暴露量。此外,更昔洛韦的治疗窗定义较为宽松。因此,在成年移植患者中系统地进行治疗药物监测的实用性似乎值得怀疑;然而,仍需要研究来扩展对特定患者亚群或剂量方案的了解。