Virological patterns of hepatitis C virus patients with failure to the current-generation direct-acting antivirals

被引:4
作者
Pisaturo, M. [1 ]
Starace, M. [1 ]
Minichini, C. [1 ]
De Pascalis, S. [2 ]
Occhiello, L. [1 ]
Di Fraia, A. [1 ]
Messina, V [3 ]
Sangiovanni, V [4 ]
Claar, E. [5 ]
Coppola, N. [1 ,2 ,6 ]
机构
[1] Univ Campania L Vanvitelli, Lab Identificat Prognost Factors Response Treatme, Naples, Italy
[2] Univ Campania L Vanvitelli, Dept Mental & Phys Hlth & Prevent Med, Infect Dis & Viral Hepatitis, Naples, Italy
[3] AO S Anna & S Sebastian, Infect Dis Unit, Caserta, Italy
[4] AORN Colli, Infect Dis Unit 3, Naples, Italy
[5] Evangel Hosp Villa Betania, Internal Med Unit, Naples, Italy
[6] Univ Campania Luigi Vanvitelli, Sect Infect Dis, Dept Mental Hlth & Publ Med, Via L Armanni 5, I-80131 Naples, Italy
关键词
Glecaprevir/pibrentasvir; Elbasvir/grazoprevir; Sofosbuvir/velpatasvir; RESISTANCE; PREVALENCE; SUBSTITUTIONS; SENSITIVITY; SOFOSBUVIR; INHIBITORS; INFECTION; VARIANTS; REGIMENS; EFFICACY;
D O I
10.1016/j.ijantimicag.2020.106067
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
There are few data on the virological characterisation of patients with failure to current-generation directacting antivirals (DAAs), namely elbasvir/grazoprevir, sofosbuvir/velpatasvir and glecaprevir/pibrentasvir. This study aimed to characterise virological patterns in patients with failure to current DAA regimens as well as the efficacy of re-treatment. All 61 consecutive hepatitis C virus (HCV) treatment-naive patients with failure to current DAAs from January 2018 to February 2019 were enrolled. Sanger sequencing of NS3, NS5A and NS5B proteins was performed using homemade protocols. NS5A resistance-associated substitutions (RASs) were more frequent in the 17 patients treated with sofosbuvir/velpatasvir (89.5%) and 33 patients treated with elbasvir/grazoprevir (97%) compared with the 11 patients treated with glecaprevir/pibrentasvir (18.2%) (P = 0.002 and 0.000, respectively). NS3 RASs were more often detected in the 33 patients with failure to elbasvir/grazoprevir (30.3%) than in the 11 patients treated with glecaprevir/pibrentasvir (9.1%). NS3 RASs were also detected in 12% of sofosbuvir/velpatasvir-treated patients. NS5B RASs were infrequently identified. Of the glecaprevir/pibrentasvir-treated patients, 73% did not show RASs in any HCV regions, a prevalence higher than that observed in those treated with elbasvir/grazoprevir (0%; P < 0.05) or sofosbuvir/velpatasvir (12%; P < 0.05). Of the 61 patients, 21 (34.4%) were re-treated with sofosbuvir/velpatasvir and voxilaprevir. All patients achieved sustained virological response at 12 weeks (SVR12). To our knowledge, this is one of the first real-life studies describing patients who failed current-generation DAAs; the prevalence of RASs differed according to the DAA regimen used, and the efficacy of re-treatment was high. (c) 2020 Elsevier B.V. and International Society of Chemotherapy. All rights reserved.
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页数:7
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