Long-Term Efficacy of Tenofovir Monotherapy for Hepatitis B Virus-Monoinfected Patients After Failure of Nucleoside/Nucleotide Analogues

被引:278
作者
van Boemmel, Florian [1 ]
de Man, Robert A. [2 ]
Wedemeyer, Heiner [3 ]
Deterding, Katja [3 ]
Petersen, Joerg [4 ]
Buggisch, Peter [4 ]
Erhardt, Andreas [5 ]
Hueppe, Dietrich
Stein, Kerstin [6 ]
Trojan, Joerg [7 ]
Sarrazin, Christoph [7 ]
Boecher, Wulf O. [8 ]
Spengler, Ulrich [9 ]
Wasmuth, Hermann E. [10 ]
Reinders, Jurrien G. P. [2 ]
Moeller, Bernd
Rhode, Peter [11 ]
Feucht, Heinz-Hubert [12 ]
Wiedenmann, Bertram [1 ]
Berg, Thomas [1 ]
机构
[1] Univ Med Berlin, Med Klin MS Hepatol & Gastroenterol Charite, D-13353 Berlin, Germany
[2] Univ Med Ctr Rotterdam, Dept Gastroenterol & Hepatol, Man Erasmus MC, Rotterdam, Netherlands
[3] Hannover Med Sch, Dept Gastroenterol Hepatol & Endocrinol, D-3000 Hannover, Germany
[4] Univ Hamburg Eppendorf, Dept Med, Hamburg, Germany
[5] Univ Klin Dusseldorf, Klin Gastroenterol Hepatol & Infektiol, Dusseldorf, Germany
[6] Univ Klinikum Heidelberg, Med Klin Gastroenterol & Infektiol 4, Heidelberg, Germany
[7] Johann Wolfgang Goethe Univ Hosp, Dept Internal Med 1, Frankfurt, Germany
[8] Johannes Gutenberg Univ Mainz, Med Klin & Poliklin 1, Mainz, Germany
[9] Univ Bonn, Dept Internal Med, D-5300 Bonn, Germany
[10] Univ Hosp Aachen, Dept Med 3, Aachen, Germany
[11] St Marien Hosp, Gastroenterol Abt, Hamm, Germany
[12] Lab Gemeinschaft Hamburg, Hamburg, Germany
关键词
IN-VITRO SUSCEPTIBILITY; HBV INFECTION; RESISTANT; ADEFOVIR; LAMIVUDINE; THERAPY; MUTATIONS; COMBINATION; NUCLEOSIDE;
D O I
10.1002/hep.23246
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Tenofovir disoproxil fumarate (TDF) has demonstrated high antiviral efficacy in treatment-naive patients with chronic hepatitis B virus (HBV) infection but experience in nucleoside/nucleotide analogue (NA)-experienced patients is limited. In this retrospective multicenter study we therefore assessed the long-term efficacy of TDF monotherapy in patients with prior failure or resistance to different NA treatments. Criteria for inclusion were HBV DNA levels >4.0 log(10) copies/mL at the start and a minimum, period of TDF therapy for at least 6 months. In all, 131 patients (mean age 42 +/- 12 years, 95 male, 65% hepatitis B e antigen [HBeAg]-positive) were eligible. Pretreatment consisted of either monotherapy with lamivudine (LAM; n = 18), adefovir (ADV, n = 8), and sequential LAM-ADV therapy (n = 73), or add-on combination therapy with both drugs (n = 29). Three patients had failed entecavir therapy. Resistance analysis in 113 of the 131 patients revealed genotypic LAM and ADV resistance in 62% and 19% of patients, respectively. The mean HBV DNA level at TDF baseline was 7.6 +/- 1.5 log(10) copies/mL The overall cumulative proportion of patients achieving HBV DNA levels <400 copies/mL was 79% after a mean treatment duration of 23 months (range, 6-60). Although LAM resistance did not influence the antiviral efficacy of TDF, the presence of ADV resistance impaired TDF efficacy (100% versus 52% probability of HBV DNA <400 copies/ml, respectively). However, virologic breakthrough was not observed in any of the patients during the entire observation period. Loss of HBeAg occurred in 24% of patients and HBsAg loss occurred in 3%. No significant adverse events were noticed during TDF monotherapy. Conclusion: TDF monotherapy induced a potent and long-lasting antiviral response in NA-experienced patients with previous treatment failure. Our data may have implications for current add-on strategies. (HEPATOLOGY 2010; 51: 73-80.)
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收藏
页码:73 / 80
页数:8
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