首页> 外文期刊>Journal of viral hepatitis. >Long-term entecavir or tenofovir disoproxil fumarate therapy in treatment-naive chronic hepatitis B patients in the real-world setting
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Long-term entecavir or tenofovir disoproxil fumarate therapy in treatment-naive chronic hepatitis B patients in the real-world setting

机译:在现实世界中,长期接受恩替卡韦或替诺福韦富马酸替诺福韦治疗的初治慢性乙型肝炎患者

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The aim of this study was to determine the long-term efficacy of entecavir (ETV) and tenofovir disoproxil fumarate (TDF) on the natural course of disease in chronic hepatitis B patients (CHB) with/without cirrhosis in clinical practice. A total of 355 treatment-naive CHB patients were enrolled into the study. The primary outcome measure was viral suppression as defined by serum HBV DNA level <20IU/mL. A secondary outcome measure was to determine the development of Hepatocellular carcinoma (HCC). Virological and biochemical responses were similar between the two treatment groups over time. The presence of cirrhosis and hepatitis B e antigen (HBeAg) positivity did not appear to impact viral suppression. The cumulative probability of HBeAg loss was 41% at 4years of therapy. Hepatitis B surface antigen (HBsAg) loss occurred in four patients. Model for End-Stage Liver Disease score was significantly improved from baseline to week 48 and 96 under antiviral therapy (P=0.013, P=0.01). HCC was diagnosed in 17 patients (4.8%). The cumulative probability of the development of HCC was 3.3% at 1year and 7.3% at 4years of therapy. The development of HCC was independently associated with older age (P=0.031) and the presence of cirrhosis (P=0.004). Serum creatinine levels and creatinine clearance remained stable over time. ETV and TDF effectively maintained virological and biochemical responses in long-term follow-up of CHB patients with/without cirrhosis. HCC may still develop, although at a lower rate, and is more likely to develop in patients with cirrhosis, especially in older patients.
机译:这项研究的目的是确定恩替卡韦(ETV)和替诺福韦富马酸替诺福韦酯(TDF)在临床上有或没有肝硬化的慢性乙型肝炎患者(CHB)的自然病程中的长期疗效。总共355名未接受过治疗的CHB患者被纳入研究。主要结果指标是病毒抑制,其定义为血清HBV DNA水平<20IU / mL。次要结果指标是确定肝细胞癌(HCC)的发展。随着时间的推移,两个治疗组之间的病毒学和生化反应相似。肝硬化和乙肝e抗原(HBeAg)阳性的出现似乎并未影响病毒抑制。治疗4年后,HBeAg丢失的累积概率为41%。乙肝表面抗原(HBsAg)丢失发生在四例患者中。在抗病毒治疗下,从基线到第48周和第96周,终末期肝病评分模型得到了显着改善(P = 0.013,P = 0.01)。在17例患者中诊断出HCC(4.8%)。治疗1年的肝癌累积概率为3.3%,治疗4年为7.3%。肝癌的发生与年龄(P = 0.031)和肝硬化(P = 0.004)独立相关。血清肌酐水平和肌酐清除率随时间保持稳定。在对有/无肝硬化的CHB患者进行长期随访时,ETV和TDF有效地保持了病毒学和生化反应。尽管肝癌的发生率较低,但仍可能发生肝癌,尤其是在老年患者中,肝癌更容易发生。

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