Real-world efficacy and safety of universal 8-week glecaprevir/pibrentasvir in patients with chronic hepatitis C with early chronic kidney disease or pre-end-stage renal disease: Insights from a nationwide hepatisis C virus registry in Taiwan.

Szu Jen Wang, Chung-Feng Huang, Te Sheng Chang, Ching Chu Lo, Chao Hung Hung, Chien Wei Huang, Lee Won Chong, Pin Nan Cheng, Ming Lun Yeh, Cheng Yuan Peng, Chien Yu Cheng, Jee Fu Huang, Ming Jong Bair, Chih Lang Lin, Chi Chieh Yang, Hsing Tao Kuo, Tsai Yuan Hsieh, Tzong Hsi Lee, Pei Lun Lee, Wen Chih Wu, Chih Lin Lin, Wei Wen Su, Sheng Shun Yang, Chia Chi Wang, Jui Ting Hu, Lein Ray Mo, Chun Ting Chen, Yi Hsiang Huang, Chun Chao Chang, Chia Sheng Huang, Guei Ying Chen, Chien Neng Kao, Chi Ming Tai, Chun Jen Liu, Mei Hsuan Lee, Pei Chien Tsai, Chia Yen Dai, Jia Horng Kao, Han Chieh Lin, Wang Long Chuang, Kuo Chih Tseng, Chi Yi Chen, Shu-Chi Wang, Ming-Lung Yu
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Abstract

An 8-week regimen of glecaprevir/pibrentasvir is recommended for treatment-naïve patients with chronic hepatitis C (CHC). In alignment with the Taiwanese government's objective to eliminate hepatitis C by 2025, this study aimed to provide real-world evidence on the use of this regimen in treatment-naïve patients with chronic kidney disease (CKD) by using data from the Taiwan Association for the Study of the Liver HCV Registry (TACR). CKD was defined by an estimated glomerular filtration rate (eGFR) of <60 mL/min/1.73 m2 or higher with proteinuria persisting for over 3 months. Patients were categorized as having early CKD (eGFR ≥45 mL/min/1.73 m2) or pre-end-stage renal disease (pre-ESRD) (eGFR <45 mL/min/1.73 m2). Among 1072 patients who received at least one dose of the regimen, 1054 had available data for assessing sustained virologic response at 12 weeks posttreatment (SVR12). The overall SVR12 rate was 99.6%, with rates of 99.7% for pre-ESRD patients and 99.6% for early CKD patients. Subgroup analysis showed 100% efficacy for genotype 3 and dyslipidemia, 99.5% for diabetes, 99.4% for cardiovascular disease, 96.9% for a history of cerebral vascular accident, and 95.5% for patients with a history of drug injection or HIV co-infection. Adverse events were reported in 16.8% of patients, with 0.8% experiencing serious events, and only two cases were treatment-related. Renal function significantly improved, with overall eGFR increasing from 39.2 to 41.9 mL/min/1.73 m2. Early CKD patients showed an eGFR rise from 53.5 to 57.1, while pre-ESRD patients improved from 27.1 to 29.2 at SVR12. The study concluded that the 8-week regimen is highly effective, well-tolerated, and associated with significant renal function improvement in treatment-naïve CHC patients with both early CKD and pre-ESRD.

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通用的8周glecaprevir/pibrentasvir治疗慢性丙型肝炎合并早期慢性肾病或终末期肾病患者的实际疗效和安全性:来自台湾全国丙型肝炎病毒登记的见解
建议对treatment-naïve慢性丙型肝炎(CHC)患者进行为期8周的glecaprevir/pibrentasvir治疗方案。​CKD的定义是肾小球滤过率(eGFR)估计为2或更高,蛋白尿持续超过3个月。患者被分类为早期CKD (eGFR≥45 mL/min/1.73 m2)或终末期肾病(esrd前)(eGFR 2)。在1072名接受至少一剂治疗方案的患者中,1054名患者在治疗后12周有持续病毒学反应评估(SVR12)的可用数据。总体SVR12率为99.6%,esrd前患者为99.7%,早期CKD患者为99.6%。亚组分析显示,基因3型和血脂异常患者有效率100%,糖尿病患者有效率99.5%,心血管疾病患者有效率99.4%,脑血管意外史患者有效率96.9%,有药物注射史或合并HIV感染患者有效率95.5%。16.8%的患者报告了不良事件,其中0.8%发生了严重事件,只有2例与治疗相关。肾功能明显改善,总eGFR从39.2增加到41.9 mL/min/1.73 m2。早期CKD患者的eGFR从53.5上升到57.1,而esrd前期患者的SVR12从27.1提高到29.2。该研究得出结论,8周的方案非常有效,耐受性良好,并且与treatment-naïve CHC合并早期CKD和esrd前患者的肾功能改善显著相关。
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