Cargando…

Adherence to pan‐genotypic glecaprevir/pibrentasvir and efficacy in HCV‐infected patients: A pooled analysis of clinical trials

BACKGROUND & AIMS: Adequate adherence to hepatitis C virus (HCV) treatment is believed to be a key component of treatment success because non‐adherence can potentially result in treatment failure and the emergence of resistant viral variants. This analysis assessed factors associated with non‐ad...

Descripción completa

Detalles Bibliográficos
Autores principales: Brown, Ashley, Welzel, Tania M., Conway, Brian, Negro, Francesco, Bräu, Norbert, Grebely, Jason, Puoti, Massimo, Aghemo, Alessio, Kleine, Henning, Pugatch, David, Mensa, Federico J., Chen, Yaozhu J., Lei, Yang, Lawitz, Eric, Asselah, Tarik
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7187170/
https://www.ncbi.nlm.nih.gov/pubmed/31568620
http://dx.doi.org/10.1111/liv.14266
_version_ 1783527116899352576
author Brown, Ashley
Welzel, Tania M.
Conway, Brian
Negro, Francesco
Bräu, Norbert
Grebely, Jason
Puoti, Massimo
Aghemo, Alessio
Kleine, Henning
Pugatch, David
Mensa, Federico J.
Chen, Yaozhu J.
Lei, Yang
Lawitz, Eric
Asselah, Tarik
author_facet Brown, Ashley
Welzel, Tania M.
Conway, Brian
Negro, Francesco
Bräu, Norbert
Grebely, Jason
Puoti, Massimo
Aghemo, Alessio
Kleine, Henning
Pugatch, David
Mensa, Federico J.
Chen, Yaozhu J.
Lei, Yang
Lawitz, Eric
Asselah, Tarik
author_sort Brown, Ashley
collection PubMed
description BACKGROUND & AIMS: Adequate adherence to hepatitis C virus (HCV) treatment is believed to be a key component of treatment success because non‐adherence can potentially result in treatment failure and the emergence of resistant viral variants. This analysis assessed factors associated with non‐adherence to glecaprevir/pibrentasvir (G/P) therapy and the impact of non‐adherence on sustained virological response at post‐treatment week 12 (SVR12) rates in HCV genotype (GT) 1‐6‐infected patients. METHODS: Adherence was calculated by pill counts at study visits during treatment, and defined as having a lowest treatment adherence of ≥80% and ≤120% at each study visit. Exploratory logistic regression modelling assessed predictors of non‐adherence to G/P therapy. SVR12 rates by treatment adherence were assessed in the intent‐to‐treat (ITT) population and modified ITT (mITT) population, which excludes non‐virological failures. RESULTS: Overall, 97% (2024/2091) of patients were adherent to G/P therapy at all consecutive study visits. Alcohol use was the only baseline characteristic independently associated with non‐adherence to G/P therapy (OR: 2.38; 95% CI: 1.13‐5.01; P = .022). In the mITT population, overall SVR12 rates were high both in patients who were adherent to G/P therapy and those who were not (99% [1983/2008] and 95% [58/61] respectively; P = .047). Corresponding SVR12 rates in the ITT population were 98% (1983/2024) and 87% (58/67) respectively. CONCLUSIONS: Most patients adhered to G/P therapy. SVR12 rates were high both in patients who were adherent to G/P treatment and those who were not. Patient education on treatment adherence should remain an important part of HCV treatment. CLINICAL TRIALS REGISTRATION: NCT02604017, NCT02640482, NCT02640157, NCT02636595, NCT02642432, NCT02651194, NCT02243293, NCT02446717.
format Online
Article
Text
id pubmed-7187170
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-71871702020-04-28 Adherence to pan‐genotypic glecaprevir/pibrentasvir and efficacy in HCV‐infected patients: A pooled analysis of clinical trials Brown, Ashley Welzel, Tania M. Conway, Brian Negro, Francesco Bräu, Norbert Grebely, Jason Puoti, Massimo Aghemo, Alessio Kleine, Henning Pugatch, David Mensa, Federico J. Chen, Yaozhu J. Lei, Yang Lawitz, Eric Asselah, Tarik Liver Int Viral Hepatitis BACKGROUND & AIMS: Adequate adherence to hepatitis C virus (HCV) treatment is believed to be a key component of treatment success because non‐adherence can potentially result in treatment failure and the emergence of resistant viral variants. This analysis assessed factors associated with non‐adherence to glecaprevir/pibrentasvir (G/P) therapy and the impact of non‐adherence on sustained virological response at post‐treatment week 12 (SVR12) rates in HCV genotype (GT) 1‐6‐infected patients. METHODS: Adherence was calculated by pill counts at study visits during treatment, and defined as having a lowest treatment adherence of ≥80% and ≤120% at each study visit. Exploratory logistic regression modelling assessed predictors of non‐adherence to G/P therapy. SVR12 rates by treatment adherence were assessed in the intent‐to‐treat (ITT) population and modified ITT (mITT) population, which excludes non‐virological failures. RESULTS: Overall, 97% (2024/2091) of patients were adherent to G/P therapy at all consecutive study visits. Alcohol use was the only baseline characteristic independently associated with non‐adherence to G/P therapy (OR: 2.38; 95% CI: 1.13‐5.01; P = .022). In the mITT population, overall SVR12 rates were high both in patients who were adherent to G/P therapy and those who were not (99% [1983/2008] and 95% [58/61] respectively; P = .047). Corresponding SVR12 rates in the ITT population were 98% (1983/2024) and 87% (58/67) respectively. CONCLUSIONS: Most patients adhered to G/P therapy. SVR12 rates were high both in patients who were adherent to G/P treatment and those who were not. Patient education on treatment adherence should remain an important part of HCV treatment. CLINICAL TRIALS REGISTRATION: NCT02604017, NCT02640482, NCT02640157, NCT02636595, NCT02642432, NCT02651194, NCT02243293, NCT02446717. John Wiley and Sons Inc. 2019-10-18 2020-04 /pmc/articles/PMC7187170/ /pubmed/31568620 http://dx.doi.org/10.1111/liv.14266 Text en © 2019 The Authors. Liver International published by John Wiley & Sons Ltd This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Viral Hepatitis
Brown, Ashley
Welzel, Tania M.
Conway, Brian
Negro, Francesco
Bräu, Norbert
Grebely, Jason
Puoti, Massimo
Aghemo, Alessio
Kleine, Henning
Pugatch, David
Mensa, Federico J.
Chen, Yaozhu J.
Lei, Yang
Lawitz, Eric
Asselah, Tarik
Adherence to pan‐genotypic glecaprevir/pibrentasvir and efficacy in HCV‐infected patients: A pooled analysis of clinical trials
title Adherence to pan‐genotypic glecaprevir/pibrentasvir and efficacy in HCV‐infected patients: A pooled analysis of clinical trials
title_full Adherence to pan‐genotypic glecaprevir/pibrentasvir and efficacy in HCV‐infected patients: A pooled analysis of clinical trials
title_fullStr Adherence to pan‐genotypic glecaprevir/pibrentasvir and efficacy in HCV‐infected patients: A pooled analysis of clinical trials
title_full_unstemmed Adherence to pan‐genotypic glecaprevir/pibrentasvir and efficacy in HCV‐infected patients: A pooled analysis of clinical trials
title_short Adherence to pan‐genotypic glecaprevir/pibrentasvir and efficacy in HCV‐infected patients: A pooled analysis of clinical trials
title_sort adherence to pan‐genotypic glecaprevir/pibrentasvir and efficacy in hcv‐infected patients: a pooled analysis of clinical trials
topic Viral Hepatitis
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7187170/
https://www.ncbi.nlm.nih.gov/pubmed/31568620
http://dx.doi.org/10.1111/liv.14266
work_keys_str_mv AT brownashley adherencetopangenotypicglecaprevirpibrentasvirandefficacyinhcvinfectedpatientsapooledanalysisofclinicaltrials
AT welzeltaniam adherencetopangenotypicglecaprevirpibrentasvirandefficacyinhcvinfectedpatientsapooledanalysisofclinicaltrials
AT conwaybrian adherencetopangenotypicglecaprevirpibrentasvirandefficacyinhcvinfectedpatientsapooledanalysisofclinicaltrials
AT negrofrancesco adherencetopangenotypicglecaprevirpibrentasvirandefficacyinhcvinfectedpatientsapooledanalysisofclinicaltrials
AT braunorbert adherencetopangenotypicglecaprevirpibrentasvirandefficacyinhcvinfectedpatientsapooledanalysisofclinicaltrials
AT grebelyjason adherencetopangenotypicglecaprevirpibrentasvirandefficacyinhcvinfectedpatientsapooledanalysisofclinicaltrials
AT puotimassimo adherencetopangenotypicglecaprevirpibrentasvirandefficacyinhcvinfectedpatientsapooledanalysisofclinicaltrials
AT aghemoalessio adherencetopangenotypicglecaprevirpibrentasvirandefficacyinhcvinfectedpatientsapooledanalysisofclinicaltrials
AT kleinehenning adherencetopangenotypicglecaprevirpibrentasvirandefficacyinhcvinfectedpatientsapooledanalysisofclinicaltrials
AT pugatchdavid adherencetopangenotypicglecaprevirpibrentasvirandefficacyinhcvinfectedpatientsapooledanalysisofclinicaltrials
AT mensafedericoj adherencetopangenotypicglecaprevirpibrentasvirandefficacyinhcvinfectedpatientsapooledanalysisofclinicaltrials
AT chenyaozhuj adherencetopangenotypicglecaprevirpibrentasvirandefficacyinhcvinfectedpatientsapooledanalysisofclinicaltrials
AT leiyang adherencetopangenotypicglecaprevirpibrentasvirandefficacyinhcvinfectedpatientsapooledanalysisofclinicaltrials
AT lawitzeric adherencetopangenotypicglecaprevirpibrentasvirandefficacyinhcvinfectedpatientsapooledanalysisofclinicaltrials
AT asselahtarik adherencetopangenotypicglecaprevirpibrentasvirandefficacyinhcvinfectedpatientsapooledanalysisofclinicaltrials