Jang Suk-Chan, Choi Won-Mook, Kim Gi-Ae, Choi Gwang Hyeon, Lee Yun Bin, Sinn Dong Hyun, Kim Hye-Lin, Lim Young-Suk
School of Pharmacy, Sungkyunkwan University, Suwon, Gyeonggi-do, Korea.
Department of Gastroenterology, Liver Center, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea.
Liver Int. 2025 Aug;45(8):e70238. doi: 10.1111/liv.70238.
BACKGROUND & AIMS: Growing evidence suggests that chronic hepatitis B (CHB) patients with high viremia are at a high risk of developing hepatocellular carcinoma (HCC) even with normal alanine transaminase (ALT) levels. This study aimed to evaluate the cost-effectiveness of initiating antiviral therapy in patients in an indeterminate phase of CHB, defined as those who do not clearly fit into the established four phases categorised by serum HBV DNA and ALT levels.
A cost-utility analysis was conducted using a Markov model to compare the incremental cost-effectiveness ratio (ICER) of initiating antiviral therapy at the indeterminate phase ('treat-Indet') versus delaying treatment until chronic hepatitis ('untreated-Indet'). A hypothetical cohort of 10 000 patients in the indeterminate phase (60% male, HBV DNA 4-8 log IU/mL, ALT < 40 IU/L, 50% HBeAg-positivity) was simulated over a 10-year horizon. Input parameters were obtained from a Korean multicentre historical cohort.
From a healthcare system perspective, the ICER of the treat-Indet strategy was US$12050/quality-adjusted life-year (QALY), indicating cost-effectiveness under the local willingness-to-pay threshold of US$25000/QALY. From a societal perspective, the ICER was less than 0, indicating lower costs. A U-shaped association was identified between baseline HBV DNA levels and the ICER, as HBV DNA levels of 6-7 log IU/mL were associated with the lowest ICER (US$2018/QALY), followed by 5-6 (US$7233/QALY), 7-8 (US$19677/QALY) and 4-5 log IU/mL (US$24570/QALY), following the order of HCC risk.
Initiating antiviral therapy in high-viremic indeterminate phase CHB patients with normal ALT levels was cost-effective compared with delaying treatment until chronic hepatitis.
越来越多的证据表明,即使丙氨酸转氨酶(ALT)水平正常,高病毒血症的慢性乙型肝炎(CHB)患者发生肝细胞癌(HCC)的风险也很高。本研究旨在评估在CHB不确定期患者中启动抗病毒治疗的成本效益,该不确定期定义为那些不符合根据血清HBV DNA和ALT水平划分的既定四个阶段的患者。
使用马尔可夫模型进行成本效用分析,以比较在不确定期启动抗病毒治疗(“不确定期治疗”)与延迟治疗直至慢性肝炎(“不确定期未治疗”)的增量成本效益比(ICER)。模拟了一个假设的队列,其中包括10000名处于不确定期的患者(60%为男性,HBV DNA 4-8 log IU/mL,ALT<40 IU/L,50% HBeAg阳性),随访期为10年。输入参数来自韩国多中心历史队列。
从医疗保健系统的角度来看,不确定期治疗策略的ICER为12050美元/质量调整生命年(QALY),表明在当地支付意愿阈值25000美元/QALY下具有成本效益。从社会角度来看,ICER小于0,表明成本更低。在基线HBV DNA水平与ICER之间发现了一种U型关联,因为HBV DNA水平为6-7 log IU/mL时ICER最低(2018美元/QALY),其次是5-6 log IU/mL(7233美元/QALY)、7-8 log IU/mL(19677美元/QALY)和4-5 log IU/mL(24570美元/QALY),与HCC风险顺序一致。
与延迟治疗直至慢性肝炎相比,在ALT水平正常的高病毒血症不确定期CHB患者中启动抗病毒治疗具有成本效益。