Luong Chieu-Hoang Ly, Ellett Lisa Kalisch, Pratt Nicole, Staff Kirsten, Janetzki Jack
Clinical and Health Sciences, University of South Australia, Adelaide, South Australia, Australia.
Quality Use of Medicines and Pharmacy Research Centre, University of South Australia, Adelaide, South Australia, Australia.
J Viral Hepat. 2025 Oct;32(10):e70082. doi: 10.1111/jvh.70082.
Direct-acting antivirals (DAAs) have transformed hepatitis C virus (HCV) treatment in Australia since their inclusion on the Pharmaceutical Benefits Scheme (PBS) in 2016. Treatment has shifted from genotype-specific to pan-genotypic regimens, with glecaprevir/pibrentasvir and sofosbuvir/velpatasvir now recommended in clinical guidelines. This study examined trends in DAA dispensing in light of evolving treatment regimens. A retrospective analysis of publicly available PBS data was conducted, assessing monthly DAA dispensings from March 2016 to December 2024. Dispensings were summarised by count and proportion, PBS item code, schedule (general, private, or public hospital) and number of repeats as a proxy for treatment duration. Dispensing volumes of DAAs increased following PBS-listing in March 2016, with the highest number of dispensings observed between 2016 and 2017 (average of 11,378 prescriptions dispensed per month). Dispensing rates subsequently declined, with an average of 1583 prescriptions dispensed per month from 2020 to 2024. Since introduction to market in August 2017, sofosbuvir with velpatasvir (pan-genotypic regimen) has maintained an average market share of 55%. Glecaprevir/pibrentasvir (pan-genotypic regimen) has maintained an average market share of 34% since its introduction in August 2018. Sofosbuvir/velpatasvir/voxilaprevir, listed on the PBS in April 2019, and used for salvage therapy, has had a smaller average market share of 4% since listing. Pan-genotypic regimens now account for nearly all DAA use in Australia. Declining dispensing rates may reflect reduced new infections and treatment fatigue. Increasing retreatment rates underscore the need for ongoing monitoring and real-world evaluations. Future head-to-head comparisons may support optimal regimen selection.
自2016年直接作用抗病毒药物(DAAs)被纳入澳大利亚药品福利计划(PBS)以来,它们改变了丙型肝炎病毒(HCV)的治疗方式。治疗方案已从基因型特异性方案转变为泛基因型方案,目前临床指南推荐使用格卡瑞韦/哌柏瑞韦和索磷布韦/维帕他韦。本研究根据不断演变的治疗方案,对DAAs配药趋势进行了研究。对公开可用的PBS数据进行了回顾性分析,评估了2016年3月至2024年12月期间每月的DAAs配药情况。配药情况按数量和比例、PBS项目代码、配药类别(普通、私人或公立医院)以及重复配药次数(作为治疗持续时间的替代指标)进行了汇总。2016年3月DAAs被列入PBS后,配药量有所增加,2016年至2017年期间配药数量最多(平均每月配药11,378张处方)。随后配药率下降,2020年至2024年期间平均每月配药1583张处方。自2017年8月上市以来,索磷布韦与维帕他韦(泛基因型方案)的平均市场份额保持在55%。格卡瑞韦/哌柏瑞韦(泛基因型方案)自2018年8月推出以来,平均市场份额保持在34%。索磷布韦/维帕他韦/伏西瑞韦于2019年4月列入PBS,用于挽救治疗,自上市以来平均市场份额较小,为4%。泛基因型方案现在几乎占澳大利亚所有DAAs的使用量。配药率下降可能反映出新感染病例减少和治疗疲劳。再治疗率上升凸显了持续监测和真实世界评估的必要性。未来的直接比较可能有助于选择最佳治疗方案。