Tenofovir disoproxil fumarate in Asian or Pacific Islander chronic hepatitis B patients with high viral load (≥ 9 log10 copies/ml)

被引:8
作者
Fung, Scott [1 ]
Gordon, Stuart C. [2 ]
Krastev, Zahary [3 ]
Horban, Andrzej [4 ]
Petersen, Joerg [5 ]
Sperl, Jan [6 ]
Gane, Edward [7 ]
Jacobson, Ira M. [8 ]
Yee, Leland J. [9 ]
Dinh, Phillip [9 ]
Martins, Eduardo B. [9 ]
Flaherty, John F. [9 ]
Kitrinos, Kathryn M. [9 ]
Dusheiko, Geoffrey [10 ]
Trinh, Huy [11 ]
Flisiak, Robert [12 ]
Rustgi, Vinod K. [13 ]
Buti, Maria [14 ,15 ]
Marcellin, Patrick [16 ]
机构
[1] Univ Toronto, Toronto, ON M5S 1A1, Canada
[2] Henry Ford Hlth Syst, Detroit, MI USA
[3] Univ Hosp, Sofia, Bulgaria
[4] Med Univ Warsaw, Warsaw, Poland
[5] Asklepios Klin St Georg, Liver Unit, Hamburg, Germany
[6] Inst Clin & Expt Med, Prague, Czech Republic
[7] Auckland City Hosp, Auckland, New Zealand
[8] Weill Cornell Med Coll, New York, NY USA
[9] Gilead Sci Inc, Foster City, CA 94404 USA
[10] Royal Free Hosp, London NW3 2QG, England
[11] San Jose Gastroenterol, San Jose, CA USA
[12] Med Univ Bialystok, Bialystok, Poland
[13] Metropolitan Liver Dis, Fairfax, VA USA
[14] Hosp Gen Univ Vall dHebron, Barcelona, Catalonia, Spain
[15] Inst Salud Carlos III, Ciberehd, Barcelona, Catalonia, Spain
[16] Univ Paris, Hop Beaujon, Clichy, France
关键词
Asian; hepatitis B; tenofovir disoproxil fumarate; viremia; E-ANTIGEN; RISK; EMTRICITABINE; EFFICACY; TDF; TRANSMISSION; MONOTHERAPY; REGRESSION; INFECTION; CIRRHOSIS;
D O I
10.1111/liv.12694
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background & AimsWe evaluated the antiviral response of Asian or Pacific Islander (API) patients with chronic hepatitis B (CHB) who had baseline high viral load (HVL), defined as pre-treatment hepatitis B virus (HBV) DNA 9 log(10) copies/ml, following up to 288weeks of tenofovir disoproxil fumarate (TDF) treatment. MethodsA total of 205 HBeAg-negative and HBeAg-positive self-described API patients received 48weeks of TDF 300mg (HVL n=18) or adefovir dipivoxil 10mg (HVL n=15) in a blinded fashion, followed by open-label TDF for an additional 240weeks. The proportions of HVL vs. non-HVL patients with HBV DNA <400 copies/ml were compared. Mean declines in HBV DNA were evaluated in API vs. non-API patients. ResultsThroughout the first 72weeks of treatment, a smaller proportion of HVL API patients reached HBV DNA <400 copies/ml than non-HVL API patients. However, after this timepoint similar proportions of HVL and non-HVL API patients achieved HBV DNA <400 copies/ml (100% vs. 97%, respectively), which was maintained through week 288, where 92% of HVL patients and 99% of non-HVL API patients on treatment had HBV DNA <400 copies/ml. During the 288weeks of treatment, API patients had similar mean HBV DNA declines as non-API patients, regardless of whether patients were HVL or non-HVL. No API HVL patient had persistent viremia at week 288. No resistance was detected among HVL or non-HVL patients. ConclusionsAPI patients with HVL CHB achieve HBV DNA <400 copies/ml with long-term TDF treatment; however, achieving viral suppression may take longer for HVL patients relative to non-HVL API patients.
引用
收藏
页码:422 / 428
页数:7
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