2nd Department of Internal Medicine, Athens University Medical School, Hippokration General Hospital, Athens, Greece.
Gut. 2011 Aug;60(8):1109-16. doi: 10.1136/gut.2010.221846. Epub 2011 Jan 26.
To evaluate the risk and predictors of hepatocellular carcinoma (HCC) in HBeAg-negative chronic hepatitis B patients of the large HEPNET.Greece cohort study who received long-term oral antivirals starting with lamivudine monotherapy.
Retrospective analysis of HCC incidence in HBeAg-negative chronic hepatitis B patients from a retrospective-prospective cohort who were treated with nucleos(t)ide analogue(s) starting with lamivudine monotherapy for ≥12 months.
A nationwide network of liver centres.
818 patients were included: 517 with chronic hepatitis B only; 160 with compensated cirrhosis; 56 with decompensated cirrhosis; 85 with unclassified disease severity.
All patients were treated with nucleos(t)ide analogue(s) starting with lamivudine monotherapy.
Development of HCC.
During a median follow-up of 4.7 years, HCC developed in 49 (6.0%) patients. The 5-year cumulative incidence of HCC was higher in patients with cirrhosis than in those with chronic hepatitis B only (11.5% vs 3.2%, respectively; p<0.001). HCC developed in 0.7%, 6.7% and 11.7% of patients <50, 50-60 and >60 years old, respectively (p<0.001). Virological on-therapy remission did not significantly affect the incidence of HCC in all patients or those with cirrhosis, but it showed a trend for lower HCC incidence in patients with chronic hepatitis B only (p=0.076). In multivariate analysis, age, gender and cirrhosis were independently associated with HCC risk regardless of virological remission.
Long-term therapy with nucleos(t)ide analogue(s) starting with lamivudine monotherapy does not eliminate HCC risk in HBeAg-negative chronic hepatitis B. The risk of HCC is particularly high in patients with cirrhosis, who should remain under HCC surveillance even during effective therapy. Older age and male gender remain independent risk factors for HCC, while virological on-therapy remission does not seem to significantly reduce the overall incidence of HCC.
评估 HBeAg 阴性慢性乙型肝炎患者接受长期口服抗病毒药物治疗(起始治疗为拉米夫定单药治疗)后发生肝细胞癌(HCC)的风险和预测因素。
对来自回顾性前瞻性队列的 HBeAg 阴性慢性乙型肝炎患者 HCC 发生率进行回顾性分析,这些患者接受核苷(酸)类似物治疗,起始治疗为拉米夫定单药治疗,治疗时间≥12 个月。
全国性肝脏中心网络。
共纳入 818 例患者:517 例慢性乙型肝炎患者;160 例代偿性肝硬化患者;56 例失代偿性肝硬化患者;85 例疾病严重程度未分类患者。
所有患者均接受核苷(酸)类似物治疗,起始治疗为拉米夫定单药治疗。
HCC 的发生。
中位随访 4.7 年后,49 例(6.0%)患者发生 HCC。肝硬化患者的 5 年 HCC 累积发生率高于单纯慢性乙型肝炎患者(分别为 11.5%和 3.2%;p<0.001)。年龄<50、50-60 和>60 岁的患者 HCC 发生率分别为 0.7%、6.7%和 11.7%(p<0.001)。病毒学治疗应答缓解并未显著影响所有患者或肝硬化患者的 HCC 发生率,但在单纯慢性乙型肝炎患者中,病毒学治疗应答缓解似乎降低了 HCC 发生率(p=0.076)。多因素分析显示,年龄、性别和肝硬化与 HCC 风险独立相关,与病毒学缓解无关。
起始治疗为拉米夫定单药治疗的核苷(酸)类似物长期治疗并不能消除 HBeAg 阴性慢性乙型肝炎患者的 HCC 风险。肝硬化患者的 HCC 风险特别高,即使在有效治疗期间,他们也应接受 HCC 监测。年龄较大和男性是 HCC 的独立危险因素,而病毒学治疗应答缓解似乎并不能显著降低 HCC 的总体发生率。