Telaprevir in the Treatment of Acute Hepatitis C Virus Infection in HIV-Infected Men

Background. There is an international epidemic of hepatitis C virus (HCV) infection among human immunodeficiency virus (HIV)–infected men who have sex with men. Sustained virologic response (SVR) rates with pegylated interferon and ribavirin treatment are higher in these men during acute HCV than du...

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Veröffentlicht in:Clinical infectious diseases 2014-03, Vol.58 (6), p.873-879
Hauptverfasser: Fierer, Daniel S., Dieterich, Douglas T., Mullen, Michael P., Branch, Andrea D., Uriel, Alison J., Carriero, Damaris C., van Seggelen, Wouter O., Hijdra, Rosanne M., Cassagnol, David G.
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container_end_page 879
container_issue 6
container_start_page 873
container_title Clinical infectious diseases
container_volume 58
creator Fierer, Daniel S.
Dieterich, Douglas T.
Mullen, Michael P.
Branch, Andrea D.
Uriel, Alison J.
Carriero, Damaris C.
van Seggelen, Wouter O.
Hijdra, Rosanne M.
Cassagnol, David G.
description Background. There is an international epidemic of hepatitis C virus (HCV) infection among human immunodeficiency virus (HIV)–infected men who have sex with men. Sustained virologic response (SVR) rates with pegylated interferon and ribavirin treatment are higher in these men during acute HCV than during chronic HCV, but treatment is still lengthy and SVR rates are suboptimal. Methods. We performed a pilot study of combination therapy with telaprevir, pegylated interferon, and ribavirin in acute genotype 1 HCV infection in HIV-infected men. Men who were treated prior to the availability of, or ineligible for, telaprevir were the comparator group. The primary endpoint was SVR12, defined as an HCV viral load
doi_str_mv 10.1093/cid/cit799
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There is an international epidemic of hepatitis C virus (HCV) infection among human immunodeficiency virus (HIV)–infected men who have sex with men. Sustained virologic response (SVR) rates with pegylated interferon and ribavirin treatment are higher in these men during acute HCV than during chronic HCV, but treatment is still lengthy and SVR rates are suboptimal. Methods. We performed a pilot study of combination therapy with telaprevir, pegylated interferon, and ribavirin in acute genotype 1 HCV infection in HIV-infected men. Men who were treated prior to the availability of, or ineligible for, telaprevir were the comparator group. The primary endpoint was SVR12, defined as an HCV viral load &lt;5 IU/mL at least 12 weeks after completing treatment. Results. In the telaprevir group, 84% (16/19) of men achieved SVR12 vs 63% (30/48) in the comparator group. Among men with SVR, median time to undetectable viral load was week 2 in the telaprevir group vs week 4 in the comparator group, and 94% vs 53% had undetectable viral loads at week 4. Most patients (81%) who achieved SVR in the telaprevir group received ≤12 weeks of treatment and there were no relapses after treatment. The overall safety profile was similar to that known for telaprevir-based regimens. Conclusions. Incorporating telaprevir into treatment of acute genotype 1 HCV in HIV-infected men halved the treatment duration and increased the SVR rate. Larger studies should be done to confirm these findings. Clinicians should be alert to detect acute HCV infection of HIV-infected men to take advantage of this effective therapy and decrease further transmission in this epidemic.</description><identifier>ISSN: 1058-4838</identifier><identifier>EISSN: 1537-6591</identifier><identifier>DOI: 10.1093/cid/cit799</identifier><identifier>PMID: 24336914</identifier><identifier>CODEN: CIDIEL</identifier><language>eng</language><publisher>Oxford: OXFORD UNIVERSITY PRESS</publisher><subject>Adult ; AIDS ; Antibiotics. Antiinfectious agents. Antiparasitic agents ; Antiretroviral drugs ; Antiviral agents ; Antiviral Agents - therapeutic use ; Biological and medical sciences ; Comparators ; Drug Therapy, Combination ; Epidemics ; Genotypes ; Hepacivirus ; Hepatitis ; Hepatitis C ; Hepatitis C - drug therapy ; Hepatitis C - virology ; HIV ; HIV infections ; HIV Infections - virology ; HIV/AIDS ; Homosexuality, Male ; Human immunodeficiency virus ; Human viral diseases ; Humans ; Infections ; Infectious diseases ; Interferon ; Interferons ; Male ; Medical sciences ; Medical treatment ; Middle Aged ; Oligopeptides - therapeutic use ; Pharmacology. Drug treatments ; Pilot Projects ; Polymerase chain reaction ; Viral diseases ; Viral diseases of the lymphoid tissue and the blood. Aids ; Viral hepatitis ; Virology</subject><ispartof>Clinical infectious diseases, 2014-03, Vol.58 (6), p.873-879</ispartof><rights>Copyright © 2014 Oxford University Press on behalf of the Infectious Diseases Society of America</rights><rights>2015 INIST-CNRS</rights><rights>Copyright Oxford University Press, UK Mar 15, 2014</rights><rights>The Author 2013. Published by Oxford University Press on behalf of the Infectious Diseases Society of America. All rights reserved. For Permissions, please e-mail: . 2013</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c491t-33837f1acdd6e199509ff610849f11fc3195d79fae12eefcf706d15b02cd26b93</citedby><cites>FETCH-LOGICAL-c491t-33837f1acdd6e199509ff610849f11fc3195d79fae12eefcf706d15b02cd26b93</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/24031725$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/24031725$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>230,314,777,781,800,882,27905,27906,57998,58231</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=28318423$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24336914$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Fierer, Daniel S.</creatorcontrib><creatorcontrib>Dieterich, Douglas T.</creatorcontrib><creatorcontrib>Mullen, Michael P.</creatorcontrib><creatorcontrib>Branch, Andrea D.</creatorcontrib><creatorcontrib>Uriel, Alison J.</creatorcontrib><creatorcontrib>Carriero, Damaris C.</creatorcontrib><creatorcontrib>van Seggelen, Wouter O.</creatorcontrib><creatorcontrib>Hijdra, Rosanne M.</creatorcontrib><creatorcontrib>Cassagnol, David G.</creatorcontrib><creatorcontrib>New York Acute Hepatitis C Surveillance Networka</creatorcontrib><creatorcontrib>New York Acute Hepatitis C Surveillance Network</creatorcontrib><creatorcontrib>for the New York Acute Hepatitis C Surveillance Network</creatorcontrib><title>Telaprevir in the Treatment of Acute Hepatitis C Virus Infection in HIV-Infected Men</title><title>Clinical infectious diseases</title><addtitle>Clin Infect Dis</addtitle><description>Background. There is an international epidemic of hepatitis C virus (HCV) infection among human immunodeficiency virus (HIV)–infected men who have sex with men. Sustained virologic response (SVR) rates with pegylated interferon and ribavirin treatment are higher in these men during acute HCV than during chronic HCV, but treatment is still lengthy and SVR rates are suboptimal. Methods. We performed a pilot study of combination therapy with telaprevir, pegylated interferon, and ribavirin in acute genotype 1 HCV infection in HIV-infected men. Men who were treated prior to the availability of, or ineligible for, telaprevir were the comparator group. The primary endpoint was SVR12, defined as an HCV viral load &lt;5 IU/mL at least 12 weeks after completing treatment. Results. In the telaprevir group, 84% (16/19) of men achieved SVR12 vs 63% (30/48) in the comparator group. Among men with SVR, median time to undetectable viral load was week 2 in the telaprevir group vs week 4 in the comparator group, and 94% vs 53% had undetectable viral loads at week 4. Most patients (81%) who achieved SVR in the telaprevir group received ≤12 weeks of treatment and there were no relapses after treatment. The overall safety profile was similar to that known for telaprevir-based regimens. Conclusions. Incorporating telaprevir into treatment of acute genotype 1 HCV in HIV-infected men halved the treatment duration and increased the SVR rate. Larger studies should be done to confirm these findings. Clinicians should be alert to detect acute HCV infection of HIV-infected men to take advantage of this effective therapy and decrease further transmission in this epidemic.</description><subject>Adult</subject><subject>AIDS</subject><subject>Antibiotics. Antiinfectious agents. Antiparasitic agents</subject><subject>Antiretroviral drugs</subject><subject>Antiviral agents</subject><subject>Antiviral Agents - therapeutic use</subject><subject>Biological and medical sciences</subject><subject>Comparators</subject><subject>Drug Therapy, Combination</subject><subject>Epidemics</subject><subject>Genotypes</subject><subject>Hepacivirus</subject><subject>Hepatitis</subject><subject>Hepatitis C</subject><subject>Hepatitis C - drug therapy</subject><subject>Hepatitis C - virology</subject><subject>HIV</subject><subject>HIV infections</subject><subject>HIV Infections - virology</subject><subject>HIV/AIDS</subject><subject>Homosexuality, Male</subject><subject>Human immunodeficiency virus</subject><subject>Human viral diseases</subject><subject>Humans</subject><subject>Infections</subject><subject>Infectious diseases</subject><subject>Interferon</subject><subject>Interferons</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Medical treatment</subject><subject>Middle Aged</subject><subject>Oligopeptides - therapeutic use</subject><subject>Pharmacology. Drug treatments</subject><subject>Pilot Projects</subject><subject>Polymerase chain reaction</subject><subject>Viral diseases</subject><subject>Viral diseases of the lymphoid tissue and the blood. 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Aids</topic><topic>Viral hepatitis</topic><topic>Virology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Fierer, Daniel S.</creatorcontrib><creatorcontrib>Dieterich, Douglas T.</creatorcontrib><creatorcontrib>Mullen, Michael P.</creatorcontrib><creatorcontrib>Branch, Andrea D.</creatorcontrib><creatorcontrib>Uriel, Alison J.</creatorcontrib><creatorcontrib>Carriero, Damaris C.</creatorcontrib><creatorcontrib>van Seggelen, Wouter O.</creatorcontrib><creatorcontrib>Hijdra, Rosanne M.</creatorcontrib><creatorcontrib>Cassagnol, David G.</creatorcontrib><creatorcontrib>New York Acute Hepatitis C Surveillance Networka</creatorcontrib><creatorcontrib>New York Acute Hepatitis C Surveillance Network</creatorcontrib><creatorcontrib>for the New York Acute Hepatitis C Surveillance Network</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Health and Safety Science Abstracts (Full archive)</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Toxicology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><collection>Safety Science and Risk</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Clinical infectious diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fierer, Daniel S.</au><au>Dieterich, Douglas T.</au><au>Mullen, Michael P.</au><au>Branch, Andrea D.</au><au>Uriel, Alison J.</au><au>Carriero, Damaris C.</au><au>van Seggelen, Wouter O.</au><au>Hijdra, Rosanne M.</au><au>Cassagnol, David G.</au><aucorp>New York Acute Hepatitis C Surveillance Networka</aucorp><aucorp>New York Acute Hepatitis C Surveillance Network</aucorp><aucorp>for the New York Acute Hepatitis C Surveillance Network</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Telaprevir in the Treatment of Acute Hepatitis C Virus Infection in HIV-Infected Men</atitle><jtitle>Clinical infectious diseases</jtitle><addtitle>Clin Infect Dis</addtitle><date>2014-03-15</date><risdate>2014</risdate><volume>58</volume><issue>6</issue><spage>873</spage><epage>879</epage><pages>873-879</pages><issn>1058-4838</issn><eissn>1537-6591</eissn><coden>CIDIEL</coden><abstract>Background. There is an international epidemic of hepatitis C virus (HCV) infection among human immunodeficiency virus (HIV)–infected men who have sex with men. Sustained virologic response (SVR) rates with pegylated interferon and ribavirin treatment are higher in these men during acute HCV than during chronic HCV, but treatment is still lengthy and SVR rates are suboptimal. Methods. We performed a pilot study of combination therapy with telaprevir, pegylated interferon, and ribavirin in acute genotype 1 HCV infection in HIV-infected men. Men who were treated prior to the availability of, or ineligible for, telaprevir were the comparator group. The primary endpoint was SVR12, defined as an HCV viral load &lt;5 IU/mL at least 12 weeks after completing treatment. Results. In the telaprevir group, 84% (16/19) of men achieved SVR12 vs 63% (30/48) in the comparator group. Among men with SVR, median time to undetectable viral load was week 2 in the telaprevir group vs week 4 in the comparator group, and 94% vs 53% had undetectable viral loads at week 4. Most patients (81%) who achieved SVR in the telaprevir group received ≤12 weeks of treatment and there were no relapses after treatment. The overall safety profile was similar to that known for telaprevir-based regimens. Conclusions. Incorporating telaprevir into treatment of acute genotype 1 HCV in HIV-infected men halved the treatment duration and increased the SVR rate. Larger studies should be done to confirm these findings. Clinicians should be alert to detect acute HCV infection of HIV-infected men to take advantage of this effective therapy and decrease further transmission in this epidemic.</abstract><cop>Oxford</cop><pub>OXFORD UNIVERSITY PRESS</pub><pmid>24336914</pmid><doi>10.1093/cid/cit799</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record>
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source MEDLINE; Jstor Complete Legacy; Oxford University Press Journals All Titles (1996-Current); EZB-FREE-00999 freely available EZB journals; Alma/SFX Local Collection
subjects Adult
AIDS
Antibiotics. Antiinfectious agents. Antiparasitic agents
Antiretroviral drugs
Antiviral agents
Antiviral Agents - therapeutic use
Biological and medical sciences
Comparators
Drug Therapy, Combination
Epidemics
Genotypes
Hepacivirus
Hepatitis
Hepatitis C
Hepatitis C - drug therapy
Hepatitis C - virology
HIV
HIV infections
HIV Infections - virology
HIV/AIDS
Homosexuality, Male
Human immunodeficiency virus
Human viral diseases
Humans
Infections
Infectious diseases
Interferon
Interferons
Male
Medical sciences
Medical treatment
Middle Aged
Oligopeptides - therapeutic use
Pharmacology. Drug treatments
Pilot Projects
Polymerase chain reaction
Viral diseases
Viral diseases of the lymphoid tissue and the blood. Aids
Viral hepatitis
Virology
title Telaprevir in the Treatment of Acute Hepatitis C Virus Infection in HIV-Infected Men
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