Division of Hepatology, Department of Internal Medicine, The Catholic University of Korea, Seoul, Republic of Korea.
The Catholic University Liver Research Center, Seoul, Republic of Korea.
Gut. 2020 Jul;69(7):1301-1308. doi: 10.1136/gutjnl-2019-318947. Epub 2019 Oct 31.
The use of tenofovir (TDF) and entecavir (ETV) in patients with chronic hepatitis B (CHB) has led to a decrease in the incidence of hepatocellular carcinoma (HCC) and liver-related events. However, whether there is a difference between the two agents in the extent of improving such outcomes has not been clarified thus far. Therefore, we aimed to compare TDF and ETV on the risk of HCC and mortality.
A total of 7015 consecutive patients with CHB who were treated with TDF or ETV between February 2007 and January 2018 at the liver units of the Catholic University of Korea were screened for study eligibility and 3022 patients were finally analysed. Study end points were HCC and all-cause mortality or liver transplantation (LT) within 5 years after the initiation of antiviral therapy. Propensity score matching (PSM) and inverse probability of treatment weighting methods were used.
No difference was observed between TDF and ETV in the incidence rates of HCC in the entire cohort (HR 1.030; 95% CI 0.703 to 1.509, PSM model, p=0.880) and subgroups of patients with chronic hepatitis and cirrhosis. Also, no difference was observed between TDF and ETV in the incidence rates of all-cause mortality or LT in the entire cohort (HR 1.090; 95% CI 0.622 to 1.911, PSM model, p=0.763), and patients with chronic hepatitis and cirrhosis.
This study has demonstrated the clinical outcomes in patients with CHB who received TDF or ETV treatment. There was no difference in the intermediate-term risk of HCC and mortality or LT between the two drugs.
替诺福韦(TDF)和恩替卡韦(ETV)在慢性乙型肝炎(CHB)患者中的应用降低了肝细胞癌(HCC)和肝脏相关事件的发生率。然而,这两种药物在改善这些结局的程度上是否存在差异,目前尚未阐明。因此,我们旨在比较 TDF 和 ETV 对 HCC 和死亡率的影响。
2007 年 2 月至 2018 年 1 月,韩国天主教大学的肝脏科共筛选了 7015 例接受 TDF 或 ETV 治疗的 CHB 连续患者,以评估其研究纳入标准,最终纳入 3022 例患者进行分析。研究终点为抗病毒治疗开始后 5 年内 HCC 和全因死亡率或肝移植(LT)。采用倾向评分匹配(PSM)和逆概率处理加权方法。
在整个队列中,TDF 和 ETV 组 HCC 的发生率无差异(HR 1.030;95%CI 0.703 至 1.509,PSM 模型,p=0.880),在慢性肝炎和肝硬化患者亚组中也无差异。在整个队列中,TDF 和 ETV 组全因死亡率或 LT 的发生率也无差异(HR 1.090;95%CI 0.622 至 1.911,PSM 模型,p=0.763),在慢性肝炎和肝硬化患者亚组中也无差异。
本研究评估了接受 TDF 或 ETV 治疗的 CHB 患者的临床结局。两种药物在 HCC 和死亡率或 LT 的中期风险方面无差异。