Mascarenhas André, Serrazina Juliana, Bronze Sérgio, Cortez-Pinto Helena, Presa José, Barreira Ana, Carrola Paulo, Vara-Luiz Francisco, Rosu-Pires Alexandra, Martins Pedro Lages, Prata Rita, Revés Joana, Bravo Catarina, Nascimento Catarina, Gouveia Catarina, Franco Ana Rita, Lima Pedro, O'Neill Catarina, Mendes Raquel R, Simão Inês Rodrigues, Santos Inês Costa, Gonçalves André Ruge, Barreiro Pedro, Mendo Rui, Barosa Rita, Figueiredo Pedro, Chagas Cristina
Department of Gastroenterology, Unidade Local de Saúde Lisboa Ocidental, Lisbon, Portugal.
Department of Gastroenterology and Hepatology, Unidade Local de Saúde Santa Maria, Lisbon, Portugal.
GE Port J Gastroenterol. 2024 Aug 30;32(3):161-173. doi: 10.1159/000540700. eCollection 2025 Jun.
Chronic infection with hepatitis C virus (HCV) causes 25% of hepatocellular carcinoma (HCC) cases worldwide, a major cause of morbimortality even after sustained virologic response (SVR). Universal screening to all patients with advanced liver fibrosis is currently recommended. A risk-based strategy could improve the detection rate of early HCC and diminish the surveillance burden. Although several risk prediction models exist, exclusion of a subgroup of patients from surveillance has not yet been recommended. The objective of this study was the comparison of the predictive accuracy of transient elastography, FIB-4, and aMAP for HCC in HCV patients after SVR in Portugal.
This was a multicentric retrospective study including patients with HCV after SVR. Comparative, univariate, multivariate, area under the ROC (receiver-operating characteristic) curve (AUC), and Youden's J-statistic analysis were performed.
HCC incidence was 4.2% (1.3/100 patient-years) after a median follow-up of 31 months with inclusion of 337 patients. All patients had a liver stiffness measurement (LSM) before SVR (considered the baseline), but only 148 (43.9%) had a transient elastography after SVR. FIB-4 and aMAP post-SVR were calculated in all patients. Multiple parameters positively correlated with HCC, but only age and baseline transient elastography remained as independent predictors in the multivariate analysis. The optimal cutoffs for prediction of HCC were baseline transient elastography 13.7 kPa, post-SVR transient elastography 16.5 and 15.8 kPa (first and last measurements, respectively), FIB-4 1.6, and aMAP 58. Baseline transient elastography revealed a fair accuracy in predicting HCC (AUC 0.776, < 0.001), with the cutoff of 13.7 kPa presenting a sensitivity of 85% and a specificity of 69%. Regarding patients who were F3-4 at baseline ( = 162), almost one-third had a baseline LSM ≤13.7 kPa ( = 51, 31.5%), an FIB-4 ≤1.6 ( = 50, 30.9%), and an aMAP score ≤58 ( = 48, 29.6%), and these cutoffs presented an NPV of 98%, 94%, and 96%, respectively, when considering HCC development.
Transient elastography (FibroScan) before SVR was a fair predictor of HCC, being more accurate than FIB-4 and aMAP. Transient elastography values ≤13.7 kPa at baseline, FIB-4 ≤1.6 and aMAP ≤58 were the cutoffs considered of low risk for HCC in a Portuguese cohort of HCV patients after SVR with advanced fibrosis. aMAP score is a risk-based surveillance tool that could improve the current HCC screening strategy, but further validation is needed.
丙型肝炎病毒(HCV)慢性感染导致全球25%的肝细胞癌(HCC)病例,即使在实现持续病毒学应答(SVR)后仍是导致发病和死亡的主要原因。目前建议对所有晚期肝纤维化患者进行普遍筛查。基于风险的策略可提高早期HCC的检出率并减轻监测负担。尽管存在多种风险预测模型,但尚未建议将某一亚组患者排除在监测之外。本研究的目的是比较葡萄牙HCV患者SVR后瞬时弹性成像、FIB-4和aMAP对HCC的预测准确性。
这是一项多中心回顾性研究,纳入SVR后的HCV患者。进行了比较、单变量、多变量、ROC(受试者工作特征)曲线下面积(AUC)和尤登J统计分析。
在纳入337例患者并进行31个月的中位随访后,HCC发病率为4.2%(1.3/100患者年)。所有患者在SVR前均进行了肝脏硬度测量(LSM)(视为基线),但SVR后仅148例(43.9%)进行了瞬时弹性成像检查。所有患者均计算了SVR后的FIB-4和aMAP。多个参数与HCC呈正相关,但多变量分析中仅年龄和基线瞬时弹性成像仍为独立预测因素。预测HCC的最佳临界值为基线瞬时弹性成像13.7 kPa、SVR后瞬时弹性成像16.5 kPa和15.8 kPa(分别为首次和末次测量值)、FIB-4 1.6和aMAP 58。基线瞬时弹性成像在预测HCC方面显示出较好的准确性(AUC 0.776,P<0.001),临界值13.7 kPa时灵敏度为85%,特异度为69%。对于基线时为F3-4期的患者(n=162),近三分之一患者的基线LSM≤13.7 kPa(n=51,31.5%)、FIB-4≤1.6(n=50,30.9%)和aMAP评分≤58(n=48,29.6%),在考虑HCC发生时,这些临界值的阴性预测值分别为98%、94%和96%。
SVR前的瞬时弹性成像(FibroScan)是HCC的较好预测指标,比FIB-4和aMAP更准确。基线时瞬时弹性成像值≤13.7 kPa、FIB-4≤1.6和aMAP≤58是葡萄牙晚期纤维化HCV患者SVR后HCC低风险的临界值。aMAP评分是一种基于风险的监测工具,可改善当前的HCC筛查策略,但需要进一步验证。