Literature DB >> 23588725

Snapshot on drug-resistance rate and profiles in patients with chronic hepatitis B receiving nucleos(t)ide analogues in clinical practice.

R Salpini1, C Alteri, V Cento, M Pollicita, V Micheli, G Gubertini, G M De Sanctis, M Visca, S Romano, C Sarrecchia, M Andreoni, M Angelico, G Parruti, V Svicher, C F Perno.   

Abstract

While the selection of complex HBV drug-resistance patterns on therapeutic failure can compromise the efficacy of anti-HBV therapies, recent data show that patients failing treatment without drug-resistance have a rate of virological success close to drug-naive patients. The goal of this study is defining, in clinical practice, the burden of drug-resistance mutations in a cohort of patients treated with anti-HBV drugs. Prevalence and patterns of drug-resistance were analyzed by RT-sequencing in 204 patients infected chronically: 148 experiencing virological rebound (defined as an increase in serum HBV-DNA > 20 IU/ml after achieving virological success [HBV-DNA < 20 IU/ml]), and 56 null/partial responders (always detectable serum HBV-DNA [>20 IU/ml] within 48 weeks of therapy). The highest rate of drug-resistance was observed in patients experiencing virological rebound (prevalence, 79.1%). Conversely, almost half (46.4%) null/partial responders have no evidence of drug-resistance. The rate of drug-resistance was higher in patients treated with lamivudine (76.8% [109/142]) and telbivudine (83.3% [5/6]), followed by adefovir (62.5% [15/24]), and entecavir (52.2% [12/23]). Complex mutational patterns characterized by the co-presence of rtM204V/I-rtA181T/V (impairing the efficacy of all anti-HBV drugs) were detected in four patients (2.7%) with virological rebound. Drug-resistance is the main cause of failure to therapy in patients experiencing virological rebound, supporting the need of rapid switch to anti-HBV drugs with higher genetic barrier and potency (entecavir/tenofovir). Conversely, nearly half of null/partial responders shows no evidence of drug-resistance mutations, maintaining high chance of achieving therapeutic success with the same class of drug. In this setting, genotypic resistance may help in selecting patients still carrying wild-type viruses, that may take major benefits from antiviral treatment.
Copyright © 2013 Wiley Periodicals, Inc.

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Year:  2013        PMID: 23588725     DOI: 10.1002/jmv.23567

Source DB:  PubMed          Journal:  J Med Virol        ISSN: 0146-6615            Impact factor:   2.327


  9 in total

1.  Evolution of drug-resistant mutations in HBV genomes in patients with treatment failure during the past seven years (2010-2016).

Authors:  Hong-Yu Zhang; Long-Gen Liu; Chun-Yan Ye; Chun-Hua Chen; Shuang-Xiong Hang; Zhen Zhu; Hong-Yu Shen; Ze-Yu Huang; Wen-Yi Chen; Yuan Xue
Journal:  Virus Genes       Date:  2017-11-08       Impact factor: 2.332

Review 2.  Treatment for hepatitis B in patients with drug resistance.

Authors:  Frank Tacke; Daniela C Kroy
Journal:  Ann Transl Med       Date:  2016-09

3.  AASLD guidelines for treatment of chronic hepatitis B.

Authors:  Norah A Terrault; Natalie H Bzowej; Kyong-Mi Chang; Jessica P Hwang; Maureen M Jonas; M Hassan Murad
Journal:  Hepatology       Date:  2015-11-13       Impact factor: 17.425

4.  Genotypic resistance profiles in Chinese patients with chronic hepatitis B virus infection and the efficacy of nucleoside analog rescue therapy.

Authors:  Ling-Bo Liang; Lan-Lan Chen; En-Qiang Chen; Juan Liao; Hong Tang
Journal:  Ther Clin Risk Manag       Date:  2015-03-12       Impact factor: 2.423

5.  Novel HBsAg mutations correlate with hepatocellular carcinoma, hamper HBsAg secretion and promote cell proliferation in vitro.

Authors:  Romina Salpini; Matteo Surdo; Nadia Warner; Maria Francesca Cortese; Danny Colledge; Sally Soppe; Maria Concetta Bellocchi; Daniele Armenia; Luca Carioti; Fabio Continenza; Domenico Di Carlo; Patrizia Saccomandi; Carmen Mirabelli; Michela Pollicita; Roberta Longo; Sara Romano; Giuseppina Cappiello; Alberto Spanò; Pascale Trimoulet; Herve Fleury; Jacopo Vecchiet; Nerio Iapadre; Angelo Barlattani; Ada Bertoli; Terenzio Mari; Caterina Pasquazzi; Gabriele Missale; Cesare Sarrecchia; Elisa Orecchini; Alessandro Michienzi; Massimo Andreoni; Simona Francioso; Mario Angelico; Jens Verheyen; Francesca Ceccherini-Silberstein; Stephen Locarnini; Carlo Federico Perno; Valentina Svicher
Journal:  Oncotarget       Date:  2017-02-28

6.  Highly Sensitive HBsAg, Anti-HBc and Anti HBsAg Titres in Early Diagnosis of HBV Reactivation in Anti-HBc-Positive Onco-Haematological Patients.

Authors:  Carlotta Cerva; Romina Salpini; Mohammad Alkhatib; Vincenzo Malagnino; Lorenzo Piermatteo; Arianna Battisti; Ada Bertoli; Jeff Gersch; Vera Holzmayer; Mary Kuhns; Gavin Cloherty; Ludovica Ferrari; Campogiani Laura; Elisabetta Teti; Maria Cantonetti; William Arcese; Francesca Ceccherini-Silberstein; Carlo-Federico Perno; Massimo Andreoni; Valentina Svicher; Loredana Sarmati
Journal:  Biomedicines       Date:  2022-02-14

7.  Profile of hepatitis B virus resistance mutations against nucleoside/nucleotide analogue treatment in Chinese patients with chronic hepatitis B.

Authors:  Jun Lei; Ying Wang; Li-Li Wang; Shao-Jun Zhang; Wei Chen; Zhi-Gang Bai; Lv-Ye Xu
Journal:  Virol J       Date:  2013-10-25       Impact factor: 4.099

Review 8.  Chronic hepatitis B: New potential therapeutic drugs target.

Authors:  Wattana Leowattana; Tawithep Leowattana
Journal:  World J Virol       Date:  2022-01-25

9.  Whole exome HBV DNA integration is independent of the intrahepatic HBV reservoir in HBeAg-negative chronic hepatitis B.

Authors:  Valentina Svicher; Romina Salpini; Lorenzo Piermatteo; Luca Carioti; Arianna Battisti; Luna Colagrossi; Rossana Scutari; Matteo Surdo; Valeria Cacciafesta; Andrea Nuccitelli; Navjyot Hansi; Francesca Ceccherini Silberstein; Carlo Federico Perno; Upkar S Gill; Patrick T F Kennedy
Journal:  Gut       Date:  2020-12-21       Impact factor: 31.793

  9 in total

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