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Are There Still Difficult-to-Treat Patients with Chronic Hepatitis C in the Era of Direct-Acting Antivirals?
Difficult-to-treat populations with chronic hepatitis C (CHC), in the era of interferon treatment, included patients with liver cirrhosis, kidney impairment, treatment-experienced individuals, and those coinfected with the human immunodeficiency virus. The current study aimed to determine whether, i...
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Published in: | Viruses 2022-01, Vol.14 (1), p.96 |
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creator | Pabjan, Paweł Brzdęk, Michał Chrapek, Magdalena Dziedzic, Kacper Dobrowolska, Krystyna Paluch, Katarzyna Garbat, Anna Błoniarczyk, Piotr Reczko, Katarzyna Stępień, Piotr Zarębska-Michaluk, Dorota |
description | Difficult-to-treat populations with chronic hepatitis C (CHC), in the era of interferon treatment, included patients with liver cirrhosis, kidney impairment, treatment-experienced individuals, and those coinfected with the human immunodeficiency virus. The current study aimed to determine whether, in the era of direct-acting antivirals (DAA), there are still patients that are difficult-to-treat. The study included all consecutive patients chronically infected with hepatitis C virus (HCV) who started interferon-free therapy between July 2015 and December 2020 in the Department of Infectious Diseases in Kielce. The analyzed real-world population consisted of 963 patients, and most of them were infected with genotype 1 (87.6%) with the predominance of subtype 1b and were treatment-naïve (78.8%). Liver cirrhosis was determined in 207 individuals (21.5%), of whom 82.6% were compensated. The overall sustained virologic response, after exclusion of non-virologic failures, was achieved in 98.4%. The univariable analysis demonstrated the significantly lower response rates in males, patients with liver cirrhosis, decompensation of hepatic function at baseline, documented esophageal varices, concomitant diabetes, body mass index ≥25, and previous ineffective antiviral treatment. Despite an overall very high effectiveness, some unfavorable factors, including male gender, genotype 3 infection, liver cirrhosis, and treatment experience, significantly reduce the chances for a virologic response were identified. |
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The current study aimed to determine whether, in the era of direct-acting antivirals (DAA), there are still patients that are difficult-to-treat. The study included all consecutive patients chronically infected with hepatitis C virus (HCV) who started interferon-free therapy between July 2015 and December 2020 in the Department of Infectious Diseases in Kielce. The analyzed real-world population consisted of 963 patients, and most of them were infected with genotype 1 (87.6%) with the predominance of subtype 1b and were treatment-naïve (78.8%). Liver cirrhosis was determined in 207 individuals (21.5%), of whom 82.6% were compensated. The overall sustained virologic response, after exclusion of non-virologic failures, was achieved in 98.4%. The univariable analysis demonstrated the significantly lower response rates in males, patients with liver cirrhosis, decompensation of hepatic function at baseline, documented esophageal varices, concomitant diabetes, body mass index ≥25, and previous ineffective antiviral treatment. Despite an overall very high effectiveness, some unfavorable factors, including male gender, genotype 3 infection, liver cirrhosis, and treatment experience, significantly reduce the chances for a virologic response were identified.</description><identifier>ISSN: 1999-4915</identifier><identifier>EISSN: 1999-4915</identifier><identifier>DOI: 10.3390/v14010096</identifier><identifier>PMID: 35062302</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Adult ; Aged ; Aged, 80 and over ; Antiviral agents ; Antiviral Agents - therapeutic use ; Body mass index ; Cirrhosis ; Coinfection ; Contraindications ; Creatinine ; Diabetes mellitus ; difficult-to-treat ; direct-acting antiviral ; Drug Therapy, Combination ; Esophagus ; Failure ; Female ; Genotype ; Genotype & phenotype ; Genotypes ; Hepacivirus - drug effects ; Hepacivirus - genetics ; Hepatitis B - complications ; Hepatitis C ; Hepatitis C, Chronic - complications ; Hepatitis C, Chronic - drug therapy ; Hepatitis C, Chronic - virology ; HIV ; HIV Infections - complications ; Human immunodeficiency virus ; Humans ; Immune system ; Infections ; Infectious diseases ; Interferon ; Laboratories ; Liver ; Liver cirrhosis ; Liver Cirrhosis - complications ; Liver diseases ; Male ; Middle Aged ; Patients ; Performance evaluation ; Sustained Virologic Response ; Treatment Failure ; Treatment Outcome ; Young Adult</subject><ispartof>Viruses, 2022-01, Vol.14 (1), p.96</ispartof><rights>2022 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2022 by the authors. 2022</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c469t-8e19e828c3542659c54c6397efc5e6c92945eca16bf864e3c92da1d8503e23e43</citedby><cites>FETCH-LOGICAL-c469t-8e19e828c3542659c54c6397efc5e6c92945eca16bf864e3c92da1d8503e23e43</cites><orcidid>0000-0001-8930-2221 ; 0000-0003-0938-1084 ; 0000-0002-1180-9230 ; 0000-0003-2480-6124</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2621380614/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2621380614?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,38516,43895,44590,53791,53793,74412,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35062302$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Pabjan, Paweł</creatorcontrib><creatorcontrib>Brzdęk, Michał</creatorcontrib><creatorcontrib>Chrapek, Magdalena</creatorcontrib><creatorcontrib>Dziedzic, Kacper</creatorcontrib><creatorcontrib>Dobrowolska, Krystyna</creatorcontrib><creatorcontrib>Paluch, Katarzyna</creatorcontrib><creatorcontrib>Garbat, Anna</creatorcontrib><creatorcontrib>Błoniarczyk, Piotr</creatorcontrib><creatorcontrib>Reczko, Katarzyna</creatorcontrib><creatorcontrib>Stępień, Piotr</creatorcontrib><creatorcontrib>Zarębska-Michaluk, Dorota</creatorcontrib><title>Are There Still Difficult-to-Treat Patients with Chronic Hepatitis C in the Era of Direct-Acting Antivirals?</title><title>Viruses</title><addtitle>Viruses</addtitle><description>Difficult-to-treat populations with chronic hepatitis C (CHC), in the era of interferon treatment, included patients with liver cirrhosis, kidney impairment, treatment-experienced individuals, and those coinfected with the human immunodeficiency virus. The current study aimed to determine whether, in the era of direct-acting antivirals (DAA), there are still patients that are difficult-to-treat. The study included all consecutive patients chronically infected with hepatitis C virus (HCV) who started interferon-free therapy between July 2015 and December 2020 in the Department of Infectious Diseases in Kielce. The analyzed real-world population consisted of 963 patients, and most of them were infected with genotype 1 (87.6%) with the predominance of subtype 1b and were treatment-naïve (78.8%). Liver cirrhosis was determined in 207 individuals (21.5%), of whom 82.6% were compensated. The overall sustained virologic response, after exclusion of non-virologic failures, was achieved in 98.4%. The univariable analysis demonstrated the significantly lower response rates in males, patients with liver cirrhosis, decompensation of hepatic function at baseline, documented esophageal varices, concomitant diabetes, body mass index ≥25, and previous ineffective antiviral treatment. Despite an overall very high effectiveness, some unfavorable factors, including male gender, genotype 3 infection, liver cirrhosis, and treatment experience, significantly reduce the chances for a virologic response were identified.</description><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Antiviral agents</subject><subject>Antiviral Agents - therapeutic use</subject><subject>Body mass index</subject><subject>Cirrhosis</subject><subject>Coinfection</subject><subject>Contraindications</subject><subject>Creatinine</subject><subject>Diabetes mellitus</subject><subject>difficult-to-treat</subject><subject>direct-acting antiviral</subject><subject>Drug Therapy, Combination</subject><subject>Esophagus</subject><subject>Failure</subject><subject>Female</subject><subject>Genotype</subject><subject>Genotype & phenotype</subject><subject>Genotypes</subject><subject>Hepacivirus - drug effects</subject><subject>Hepacivirus - genetics</subject><subject>Hepatitis B - 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The current study aimed to determine whether, in the era of direct-acting antivirals (DAA), there are still patients that are difficult-to-treat. The study included all consecutive patients chronically infected with hepatitis C virus (HCV) who started interferon-free therapy between July 2015 and December 2020 in the Department of Infectious Diseases in Kielce. The analyzed real-world population consisted of 963 patients, and most of them were infected with genotype 1 (87.6%) with the predominance of subtype 1b and were treatment-naïve (78.8%). Liver cirrhosis was determined in 207 individuals (21.5%), of whom 82.6% were compensated. The overall sustained virologic response, after exclusion of non-virologic failures, was achieved in 98.4%. The univariable analysis demonstrated the significantly lower response rates in males, patients with liver cirrhosis, decompensation of hepatic function at baseline, documented esophageal varices, concomitant diabetes, body mass index ≥25, and previous ineffective antiviral treatment. Despite an overall very high effectiveness, some unfavorable factors, including male gender, genotype 3 infection, liver cirrhosis, and treatment experience, significantly reduce the chances for a virologic response were identified.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>35062302</pmid><doi>10.3390/v14010096</doi><orcidid>https://orcid.org/0000-0001-8930-2221</orcidid><orcidid>https://orcid.org/0000-0003-0938-1084</orcidid><orcidid>https://orcid.org/0000-0002-1180-9230</orcidid><orcidid>https://orcid.org/0000-0003-2480-6124</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Adult Aged Aged, 80 and over Antiviral agents Antiviral Agents - therapeutic use Body mass index Cirrhosis Coinfection Contraindications Creatinine Diabetes mellitus difficult-to-treat direct-acting antiviral Drug Therapy, Combination Esophagus Failure Female Genotype Genotype & phenotype Genotypes Hepacivirus - drug effects Hepacivirus - genetics Hepatitis B - complications Hepatitis C Hepatitis C, Chronic - complications Hepatitis C, Chronic - drug therapy Hepatitis C, Chronic - virology HIV HIV Infections - complications Human immunodeficiency virus Humans Immune system Infections Infectious diseases Interferon Laboratories Liver Liver cirrhosis Liver Cirrhosis - complications Liver diseases Male Middle Aged Patients Performance evaluation Sustained Virologic Response Treatment Failure Treatment Outcome Young Adult |
title | Are There Still Difficult-to-Treat Patients with Chronic Hepatitis C in the Era of Direct-Acting Antivirals? |
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