Department of Nephrology, Royal Perth Hospital, Perth, WA, Australia.
Department of Nephrology, Fraser Coast Hospital and Health Service, Hervey Bay, QLD, Australia.
BMC Nephrol. 2021 Dec 2;22(1):400. doi: 10.1186/s12882-021-02607-4.
Tolvaptan is the only available disease-modifying treatment for autosomal dominant polycystic kidney disease (ADPKD). Prior to October 2020 access to tolvaptan in Australia was restricted by a controlled monitoring and distribution program called IMADJIN®. Focusing on hepatic safety, the IMADJIN® program collected real-world data on patients with ADPKD. A retrospective, secondary data analysis of the IMADJIN® dataset was undertaken to determine the time to all-cause discontinuation of tolvaptan in Australia.
Demographic and treatment data from 17 September 2018 to 30 September 2020 were extracted from the IMADJIN® dataset. Treatment persistence was analyzed using Kaplan-Meier methods, and Cox's proportional hazard models were used to analyze differences in treatment persistence by age, sex and location.
Four hundred seventy-nine patients with ADPKD were included in the analysis. After a median follow-up of 12.0 months (95% confidence interval [CI] 2.6, 23.4), the Kaplan-Meier estimation of 12-month persistence was 76.7% (95% CI 72.2, 80.5%). 114 (23.8%) patients discontinued treatment; sex, state, and remoteness did not significantly affect treatment persistence. Patients in the youngest tertile were more likely to discontinue compared to older ages (p = 0.049). Reasons for discontinuation included: aquaretic tolerability (4.2%), hepatic adverse events (abnormal liver function tests) (2.1%), disease progression (1.5%), and acute kidney injury (0.2%). Patients with a lack of aquaretic tolerance had shorter time to discontinuation. Hepatic toxicity events were initially observed 3 months after tolvaptan initiation and were less prevalent over time.
Persistence to tolvaptan in the real-world IMADJIN® dataset was 76%. Discontinuation due to hepatic events was low. Prescribers should take extra care when initiating treatment in younger patients as they are more likely to discontinue tolvaptan compared to older individuals. Nevertheless, the precise reason for this observation remains to be elucidated.
托伐普坦是治疗常染色体显性多囊肾病(ADPKD)的唯一可用的疾病修正治疗药物。在 2020 年 10 月之前,托伐普坦在澳大利亚的使用受到名为“IMADJIN”的受控监测和分配计划的限制。该计划专注于肝安全性,收集了 ADPKD 患者的真实世界数据。对“IMADJIN”数据集进行了回顾性二次数据分析,以确定澳大利亚托伐普坦停药的全因时间。
从 2018 年 9 月 17 日至 2020 年 9 月 30 日,从“IMADJIN”数据集提取人口统计学和治疗数据。使用 Kaplan-Meier 方法分析治疗持久性,并使用 Cox 比例风险模型分析年龄、性别和地点对治疗持久性的差异。
纳入了 479 例 ADPKD 患者进行分析。中位随访 12.0 个月(95%置信区间[CI]2.6,23.4)后,Kaplan-Meier 估计的 12 个月的持久性为 76.7%(95%CI72.2,80.5%)。114(23.8%)名患者停止治疗;性别、州和偏远程度并未显著影响治疗持久性。最年轻的三分位组患者比年龄较大的患者更有可能停药(p=0.049)。停药的原因包括:利尿性耐受性(4.2%)、肝不良反应(肝功能异常)(2.1%)、疾病进展(1.5%)和急性肾损伤(0.2%)。缺乏利尿耐受性的患者停药时间更短。肝毒性事件最初在托伐普坦开始后 3 个月观察到,随着时间的推移,其发生率较低。
在真实世界的“IMADJIN”数据集中,托伐普坦的持久性为 76%。由于肝事件导致的停药率较低。在为年龄较小的患者开始治疗时,应格外小心,因为与年龄较大的个体相比,他们更有可能停止使用托伐普坦。然而,这一观察结果的确切原因仍有待阐明。