Rademaker Tessa, Chu Rachel, Hasan Suhaila, Harris Anthony, Alffenaar Jan-Willem
School of Pharmacy, Faculty of Science, Utrecht University, Utrecht, the Netherlands.
School of Pharmacy, Faculty of Medicine and Health, University of Sydney, Australia.
Pharmacol Res Perspect. 2025 Oct;13(5):e70165. doi: 10.1002/prp2.70165.
Clozapine is superior in the treatment of treatment-refractory schizophrenia but requires therapeutic drug monitoring (TDM) due to its unpredictable pharmacokinetics and dose-dependent side effects. This systematic review evaluates saliva as a more patient-friendly sampling strategy for clozapine TDM. A systematic search was carried out using MEDLINE, Embase, APA PsycInfo, and Cochrane Central Register of Controlled Trials (CCTR) through Ovid. Studies were eligible for inclusion if data on clozapine pharmacokinetics in saliva were described. To assess the feasibility of saliva for the TDM of clozapine, ease of saliva collection, method of detection, detectability of clozapine in saliva, correlation of clozapine concentrations in saliva compared to blood, clozapine stability in saliva, and clinical validation were taken into account. A total of nine studies were included. Overall, the collection of saliva was considered simple, less invasive, and quick compared to the collection of blood. Clozapine was found stable for up to 6 months when stored at -20°C. Various methods were used for the detection of clozapine with a lower limit of detection (LLOQ) ranging from 0.1 to 15 ng/mL. Clozapine saliva concentrations between 8.50 ng/mL and 2,720 ng/mL were observed, and no correlation between clozapine levels in saliva and blood was found. Although saliva is a promising specimen for the TDM of clozapine, no clear recommendation could be made to replace blood with saliva due to methodological issues with the included studies. For this reason, further clinical validation studies are needed.
氯氮平在治疗难治性精神分裂症方面效果更佳,但因其不可预测的药代动力学和剂量依赖性副作用,需要进行治疗药物监测(TDM)。本系统评价评估唾液作为氯氮平TDM一种更方便患者的采样策略。通过Ovid使用MEDLINE、Embase、APA PsycInfo和Cochrane对照试验中央注册库(CCTR)进行了系统检索。如果描述了唾液中氯氮平药代动力学的数据,则这些研究符合纳入标准。为了评估唾液用于氯氮平TDM的可行性,考虑了唾液采集的难易程度、检测方法、唾液中氯氮平的可检测性、唾液与血液中氯氮平浓度的相关性、氯氮平在唾液中的稳定性以及临床验证。总共纳入了9项研究。总体而言,与采集血液相比,唾液采集被认为简单、侵入性小且快速。发现氯氮平在-20°C下储存长达6个月时是稳定的。使用了各种方法检测氯氮平,检测下限(LLOQ)范围为0.1至15 ng/mL。观察到唾液中氯氮平浓度在8.50 ng/mL至2720 ng/mL之间,且未发现唾液与血液中氯氮平水平之间存在相关性。尽管唾液是氯氮平TDM的一种有前景的标本,但由于纳入研究存在方法学问题,无法明确建议用唾液替代血液。因此,需要进一步的临床验证研究。