Pastras Ploutarchos, Zazas Evaggelos, Kalafateli Maria, Aggeletopoulou Ioanna, Tsounis Efthymios P, Kanaloupitis Stavros, Zisimopoulos Konstantinos, Kottaridou Eirini-Eleni-Konstantina, Antonopoulou Aspasia, Drakopoulos Dimosthenis, Diamantopoulou Georgia, Tsintoni Aggeliki, Thomopoulos Konstantinos, Triantos Christos
Division of Gastroenterology, Department of Internal Medicine, University Hospital of Patras, 26504 Patras, Greece.
Department of Internal Medicine, University Hospital of Patras, 26504 Patras, Greece.
Cancers (Basel). 2024 Jul 12;16(14):2521. doi: 10.3390/cancers16142521.
Chronic hepatitis B (CHB) infection constitutes a leading cause of hepatocellular carcinoma (HCC) development. The identification of HCC risk factors and the development of prognostic risk scores are essential for early diagnosis and prognosis. The aim of this observational, retrospective study was to evaluate baseline risk factors associated with HCC in CHB. Six hundred thirty-two consecutive adults with CHB ( = 632) [median age: 46 (IQR: 24)], attending the outpatients' Hepatology clinics between 01/1993-09/2020 were evaluated. Core promoter mutations and cirrhosis-HCC (GAG-HCC), Chinese University-HCC (CU-HCC), risk estimation for hepatocellular carcinoma in chronic hepatitis B (REACH-B), Fibrosis-4 (FIB-4), and Platelet Age Gender-HBV (PAGE-B) prognostic scores were calculated, and receiver operating curves were used to assess their prognostic performance. HCC was developed in 34 (5.38%) patients. In the multivariable Cox regression analysis, advanced age (HR: 1.086, 95% CI: 1.037-1.137), male sex (HR: 7.696, 95% CI: 1.971-30.046), alcohol abuse (HR: 2.903, 95% CI: 1.222-6.987) and cirrhosis (HR: 21.239, 95% CI: 6.001-75.167) at baseline were independently associated with the development of HCC. GAG-HCC and PAGE-B showed the highest performance with c-statistics of 0.895 (95% CI: 0.829-0.961) and 0.857 (95% CI: 0.791-0.924), respectively. In the subgroup of patients with cirrhosis, the performance of all scores declined. When treated and untreated patients were studied separately, the discriminatory ability of the scores differed. In conclusion, HCC development was independently associated with advanced age, male sex, alcohol abuse, and baseline cirrhosis among a diverse population with CHB. GAG-HCC and PAGE-B showed high discriminatory performance to assess the risk of HCC development in these patients, but these performances declined in the subgroup of patients with cirrhosis. Further research to develop scores more specific to certain CHB subgroups is needed.
慢性乙型肝炎(CHB)感染是肝细胞癌(HCC)发生的主要原因。识别HCC危险因素并制定预后风险评分对于早期诊断和预后至关重要。这项观察性、回顾性研究的目的是评估CHB中与HCC相关的基线危险因素。对1993年1月至2020年9月期间在门诊肝病诊所就诊的632例连续成年CHB患者(n = 632)[中位年龄:46岁(四分位间距:24)]进行了评估。计算了核心启动子突变与肝硬化-HCC(GAG-HCC)、香港中文大学-HCC(CU-HCC)、慢性乙型肝炎肝细胞癌风险评估(REACH-B)、纤维化-4(FIB-4)和血小板年龄性别-HBV(PAGE-B)预后评分,并使用受试者工作曲线评估其预后性能。34例(5.38%)患者发生了HCC。在多变量Cox回归分析中,高龄(HR:1.086,95%CI:1.037 - 1.137)、男性(HR:7.696,95%CI:1.971 - 30.046)、酗酒(HR:2.903,95%CI:1.222 - 6.987)和基线肝硬化(HR:21.239,95%CI:6.001 - 75.167)与HCC的发生独立相关。GAG-HCC和PAGE-B表现最佳,c统计量分别为0.895(95%CI:0.829 - 0.961)和0.857(95%CI:0.791 - 0.924)。在肝硬化患者亚组中,所有评分的性能均下降。当分别研究治疗和未治疗的患者时,评分的鉴别能力有所不同。总之,在不同的CHB人群中,HCC的发生与高龄、男性、酗酒和基线肝硬化独立相关。GAG-HCC和PAGE-B在评估这些患者发生HCC的风险方面表现出较高的鉴别性能,但在肝硬化患者亚组中这些性能下降。需要进一步研究开发更针对某些CHB亚组的评分。