Department of Virology and Liver Unit, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan.
Department of General Internal Medicine, Kyushu University Hospital, Fukuoka, Japan.
Hepatol Int. 2020 Dec;14(6):1023-1033. doi: 10.1007/s12072-020-10105-2. Epub 2020 Dec 4.
Despite HCV cure, patients remain at risk for HCC, but risk factor data for HCC following SVR are limited for Asian patients.
To address this gap, we analyzed 5814 patients (5646 SVR, 168 non-SVR) from the Real-World Evidence from the Asia Liver Consortium for HCV (REAL-C) who did not have HCC or a history of HCC at baseline (pre-DAA treatment) and did not develop HCC within 6 months of baseline. To assess the effect of SVR on HCC incidence, we used 1:4 propensity score matching [(PSM), age, sex, baseline cirrhosis, and baseline AFP] to balance the SVR and non-SVR groups.
In the PSM cohort (160 non-SVR and 612 SVR), the HCC incidence rate per 100 person years was higher in the non-SVR compared to the SVR group (5.26 vs. 1.94, p < 0.001). Achieving SVR was independently associated with decreased HCC risk (adjusted HR [aHR]: 0.41, p = 0.002). Next, we stratified the SVR cohort of 5646 patients to cirrhotic and noncirrhotic subgroups. Among cirrhotic SVR patients, aged ≥ 60, having an albumin bilirubin grade (ALBI) of 2 or 3 (aHR: 2.5, p < 0.001), and baseline AFP ≥ 10 ng/mL (aHR: 1.6, p = 0.001) were associated with higher HCC risk, while among the non-cirrhotic SVR group, only baseline AFP ≥ 10 ng/mL was significant (aHR: 4.26, p = 0.005).
Achieving SVR decreases HCC risk; however, among East Asians, patients with elevated pretreatment AFP remained at risk. Pretreatment AFP, an easily obtained serum marker, may provide both prognostic and surveillance value for HCC in East Asian patients who obtained SVR.
尽管 HCV 已被治愈,但患者仍有发生 HCC 的风险,但对于 SVR 后的亚洲患者,有关 HCC 的风险因素数据有限。
为了解决这一差距,我们分析了来自亚洲肝脏联盟 HCV 真实世界证据(REAL-C)的 5814 名患者(5646 名 SVR,168 名非 SVR)的数据,这些患者在基线(DAA 治疗前)时没有 HCC 或 HCC 病史,并且在基线后 6 个月内没有发生 HCC。为了评估 SVR 对 HCC 发生率的影响,我们使用 1:4 的倾向评分匹配(PSM)[年龄、性别、基线肝硬化和基线 AFP]来平衡 SVR 和非 SVR 组。
在 PSM 队列(160 名非 SVR 和 612 名 SVR)中,非 SVR 组的 HCC 发生率(每 100 人年 5.26)高于 SVR 组(每 100 人年 1.94,p<0.001)。获得 SVR 与 HCC 风险降低独立相关(调整后的 HR [aHR]:0.41,p=0.002)。接下来,我们对 5646 名 SVR 患者的队列进行了分层,分为肝硬化和非肝硬化亚组。在肝硬化 SVR 患者中,年龄≥60 岁、ALBI 分级为 2 或 3(aHR:2.5,p<0.001)以及基线 AFP≥10ng/mL(aHR:1.6,p=0.001)与更高的 HCC 风险相关,而非肝硬化 SVR 组中仅基线 AFP≥10ng/mL 有意义(aHR:4.26,p=0.005)。
获得 SVR 可降低 HCC 风险;然而,在东亚人群中,基线 AFP 升高的患者仍有风险。基线 AFP 是一种易于获得的血清标志物,它可能为获得 SVR 的东亚患者的 HCC 提供预后和监测价值。