Treatment of acute hepatitis C in human immunodeficiency virus–infected patients: The HEPAIG study
Acute hepatitis C continues to be a concern in men who have sex with men (MSM), and its optimal management has yet to be established. In this study, the clinical, biological, and therapeutic data of 53 human immunodeficiency virus (HIV)‐infected MSM included in a multicenter prospective study on acu...
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creator | Piroth, Lionel Larsen, Christine Binquet, Christine Alric, Laurent Auperin, Isabelle Chaix, Marie‐Laure Dominguez, Stéphanie Duval, Xavier Gervais, Anne Ghosn, Jade Delarocque‐Astagneau, Elisabeth Pol, Stanislas |
description | Acute hepatitis C continues to be a concern in men who have sex with men (MSM), and its optimal management has yet to be established. In this study, the clinical, biological, and therapeutic data of 53 human immunodeficiency virus (HIV)‐infected MSM included in a multicenter prospective study on acute hepatitis C in 2006‐2007 were retrospectively collected and analyzed. The mean hepatitis C virus (HCV) viral load at diagnosis was 5.8 ± 1.1 log10 IU/mL (genotype 4, n = 28; genotype 1, n = 14, genotype 3, n = 7). The cumulative rates of spontaneous HCV clearance were 11.0% and 16.5% 3 and 6 months after diagnosis, respectively. Forty patients were treated, 38 of whom received pegylated interferon and ribavirin. The mean duration of HCV therapy was 39 ± 17 weeks (24 ± 4 weeks in 14 cases). On treatment, 18/36 (50.0%; 95% confidence interval 34.3‐65.7) patients had undetectable HCV RNA at week 4 (RVR), and 32/39 (82.1%; 95 confidence interval 70.0‐94.1) achieved sustained virological response (SVR). SVR did not correlate with pretreatment parameters, including HCV genotype, but correlated with RVR (predictive positive value of 94.4%) and with effective duration of HCV therapy (64.3% for 24 ± 4 weeks versus 92.0% for longer treatment; P = 0.03). Conclusion: The low rate of spontaneous clearance and the high SVR rates argue for early HCV therapy following diagnosis of acute hepatitis C in HIV‐infected MSM. Pegylated interferon and ribavirin seem to be the best option. The duration of treatment should be modulated according to RVR, with a 24‐week course for patients presenting RVR and a 48‐week course for those who do not, irrespectively of HCV genotype. (HEPATOLOGY 2010) |
doi_str_mv | 10.1002/hep.23959 |
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In this study, the clinical, biological, and therapeutic data of 53 human immunodeficiency virus (HIV)‐infected MSM included in a multicenter prospective study on acute hepatitis C in 2006‐2007 were retrospectively collected and analyzed. The mean hepatitis C virus (HCV) viral load at diagnosis was 5.8 ± 1.1 log10 IU/mL (genotype 4, n = 28; genotype 1, n = 14, genotype 3, n = 7). The cumulative rates of spontaneous HCV clearance were 11.0% and 16.5% 3 and 6 months after diagnosis, respectively. Forty patients were treated, 38 of whom received pegylated interferon and ribavirin. The mean duration of HCV therapy was 39 ± 17 weeks (24 ± 4 weeks in 14 cases). On treatment, 18/36 (50.0%; 95% confidence interval 34.3‐65.7) patients had undetectable HCV RNA at week 4 (RVR), and 32/39 (82.1%; 95 confidence interval 70.0‐94.1) achieved sustained virological response (SVR). SVR did not correlate with pretreatment parameters, including HCV genotype, but correlated with RVR (predictive positive value of 94.4%) and with effective duration of HCV therapy (64.3% for 24 ± 4 weeks versus 92.0% for longer treatment; P = 0.03). Conclusion: The low rate of spontaneous clearance and the high SVR rates argue for early HCV therapy following diagnosis of acute hepatitis C in HIV‐infected MSM. Pegylated interferon and ribavirin seem to be the best option. The duration of treatment should be modulated according to RVR, with a 24‐week course for patients presenting RVR and a 48‐week course for those who do not, irrespectively of HCV genotype. (HEPATOLOGY 2010)</description><identifier>ISSN: 0270-9139</identifier><identifier>EISSN: 1527-3350</identifier><identifier>DOI: 10.1002/hep.23959</identifier><identifier>PMID: 21064156</identifier><identifier>CODEN: HPTLD9</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Acute Disease ; Adult ; Antiviral Agents - therapeutic use ; Biological and medical sciences ; Gastroenterology. Liver. Pancreas. Abdomen ; Hepatitis C ; Hepatitis C - complications ; Hepatitis C - drug therapy ; Hepatitis C Antibodies - analysis ; Hepatitis C virus ; Hepatology ; HIV Infections - complications ; HIV Infections - drug therapy ; Human immunodeficiency virus ; Human viral diseases ; Humans ; Infectious diseases ; Interferon-alpha - therapeutic use ; Lentivirus ; Liver. Biliary tract. Portal circulation. Exocrine pancreas ; Male ; Medical sciences ; Middle Aged ; Polyethylene Glycols - therapeutic use ; Recombinant Proteins ; Retrospective Studies ; Retroviridae ; Viral diseases ; Viral diseases of the lymphoid tissue and the blood. Aids ; Viral hepatitis ; Viral Load - drug effects</subject><ispartof>Hepatology (Baltimore, Md.), 2010-12, Vol.52 (6), p.1915-1921</ispartof><rights>Copyright © 2010 American Association for the Study of Liver Diseases</rights><rights>2015 INIST-CNRS</rights><rights>Copyright © 2010 American Association for the Study of Liver Diseases.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4159-7962a5b35b42a91aa4e2db794645ebb3ca884ea212b4b95141902ca0a079e3373</citedby><cites>FETCH-LOGICAL-c4159-7962a5b35b42a91aa4e2db794645ebb3ca884ea212b4b95141902ca0a079e3373</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fhep.23959$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fhep.23959$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=23630954$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21064156$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Piroth, Lionel</creatorcontrib><creatorcontrib>Larsen, Christine</creatorcontrib><creatorcontrib>Binquet, Christine</creatorcontrib><creatorcontrib>Alric, Laurent</creatorcontrib><creatorcontrib>Auperin, Isabelle</creatorcontrib><creatorcontrib>Chaix, Marie‐Laure</creatorcontrib><creatorcontrib>Dominguez, Stéphanie</creatorcontrib><creatorcontrib>Duval, Xavier</creatorcontrib><creatorcontrib>Gervais, Anne</creatorcontrib><creatorcontrib>Ghosn, Jade</creatorcontrib><creatorcontrib>Delarocque‐Astagneau, Elisabeth</creatorcontrib><creatorcontrib>Pol, Stanislas</creatorcontrib><creatorcontrib>Steering Committee of the HEPAIG Study</creatorcontrib><title>Treatment of acute hepatitis C in human immunodeficiency virus–infected patients: The HEPAIG study</title><title>Hepatology (Baltimore, Md.)</title><addtitle>Hepatology</addtitle><description>Acute hepatitis C continues to be a concern in men who have sex with men (MSM), and its optimal management has yet to be established. In this study, the clinical, biological, and therapeutic data of 53 human immunodeficiency virus (HIV)‐infected MSM included in a multicenter prospective study on acute hepatitis C in 2006‐2007 were retrospectively collected and analyzed. The mean hepatitis C virus (HCV) viral load at diagnosis was 5.8 ± 1.1 log10 IU/mL (genotype 4, n = 28; genotype 1, n = 14, genotype 3, n = 7). The cumulative rates of spontaneous HCV clearance were 11.0% and 16.5% 3 and 6 months after diagnosis, respectively. Forty patients were treated, 38 of whom received pegylated interferon and ribavirin. The mean duration of HCV therapy was 39 ± 17 weeks (24 ± 4 weeks in 14 cases). On treatment, 18/36 (50.0%; 95% confidence interval 34.3‐65.7) patients had undetectable HCV RNA at week 4 (RVR), and 32/39 (82.1%; 95 confidence interval 70.0‐94.1) achieved sustained virological response (SVR). SVR did not correlate with pretreatment parameters, including HCV genotype, but correlated with RVR (predictive positive value of 94.4%) and with effective duration of HCV therapy (64.3% for 24 ± 4 weeks versus 92.0% for longer treatment; P = 0.03). Conclusion: The low rate of spontaneous clearance and the high SVR rates argue for early HCV therapy following diagnosis of acute hepatitis C in HIV‐infected MSM. Pegylated interferon and ribavirin seem to be the best option. The duration of treatment should be modulated according to RVR, with a 24‐week course for patients presenting RVR and a 48‐week course for those who do not, irrespectively of HCV genotype. (HEPATOLOGY 2010)</description><subject>Acute Disease</subject><subject>Adult</subject><subject>Antiviral Agents - therapeutic use</subject><subject>Biological and medical sciences</subject><subject>Gastroenterology. Liver. Pancreas. Abdomen</subject><subject>Hepatitis C</subject><subject>Hepatitis C - complications</subject><subject>Hepatitis C - drug therapy</subject><subject>Hepatitis C Antibodies - analysis</subject><subject>Hepatitis C virus</subject><subject>Hepatology</subject><subject>HIV Infections - complications</subject><subject>HIV Infections - drug therapy</subject><subject>Human immunodeficiency virus</subject><subject>Human viral diseases</subject><subject>Humans</subject><subject>Infectious diseases</subject><subject>Interferon-alpha - therapeutic use</subject><subject>Lentivirus</subject><subject>Liver. Biliary tract. Portal circulation. Exocrine pancreas</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Polyethylene Glycols - therapeutic use</subject><subject>Recombinant Proteins</subject><subject>Retrospective Studies</subject><subject>Retroviridae</subject><subject>Viral diseases</subject><subject>Viral diseases of the lymphoid tissue and the blood. Aids</subject><subject>Viral hepatitis</subject><subject>Viral Load - drug effects</subject><issn>0270-9139</issn><issn>1527-3350</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp90U9rFDEYBvAgit1WD34BCYjUHqbN_0y8laW2hYIe1vOQybzDpsxk1mRS2ZvfwW_oJzF11wqFesrll-dN3gehN5ScUkLY2Ro2p4wbaZ6hBZVMV5xL8hwtCNOkMpSbA3SY0i0hxAhWv0QHjBIlqFQL1K0i2HmEMOOpx9blGXCJs7OffcJL7ANe59EG7Mcxh6mD3jsPwW3xnY85_frx04ce3Awdvr9UctJHvFoDvrr4cn59idOcu-0r9KK3Q4LX-_MIff10sVpeVTefL6-X5zeVK48xlTaKWdly2QpmDbVWAOtabYQSEtqWO1vXAiyjrBWtkVRQQ5izxBJtgHPNj9DxLncTp28Z0tyMPjkYBhtgyqmpKaNcGV0X-eG_kmqtlNKMmkLfPaK3U46h_KMopWrGFFVFneyUi1NKEfpmE_1o47ahpLkvqSlbbf6UVOzbfWJuR-ge5N9WCni_BzY5O_TRBufTP8cVJ0aK4s527rsfYPv0xKaUsRv9G8vKp2Y</recordid><startdate>201012</startdate><enddate>201012</enddate><creator>Piroth, Lionel</creator><creator>Larsen, Christine</creator><creator>Binquet, Christine</creator><creator>Alric, Laurent</creator><creator>Auperin, Isabelle</creator><creator>Chaix, Marie‐Laure</creator><creator>Dominguez, Stéphanie</creator><creator>Duval, Xavier</creator><creator>Gervais, Anne</creator><creator>Ghosn, Jade</creator><creator>Delarocque‐Astagneau, Elisabeth</creator><creator>Pol, Stanislas</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley</general><general>Wolters Kluwer Health, Inc</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7T5</scope><scope>7TM</scope><scope>7TO</scope><scope>7U9</scope><scope>H94</scope><scope>K9.</scope><scope>7X8</scope></search><sort><creationdate>201012</creationdate><title>Treatment of acute hepatitis C in human immunodeficiency virus–infected patients: The HEPAIG study</title><author>Piroth, Lionel ; Larsen, Christine ; Binquet, Christine ; Alric, Laurent ; Auperin, Isabelle ; Chaix, Marie‐Laure ; Dominguez, Stéphanie ; Duval, Xavier ; Gervais, Anne ; Ghosn, Jade ; Delarocque‐Astagneau, Elisabeth ; Pol, Stanislas</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4159-7962a5b35b42a91aa4e2db794645ebb3ca884ea212b4b95141902ca0a079e3373</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Acute Disease</topic><topic>Adult</topic><topic>Antiviral Agents - therapeutic use</topic><topic>Biological and medical sciences</topic><topic>Gastroenterology. Liver. Pancreas. Abdomen</topic><topic>Hepatitis C</topic><topic>Hepatitis C - complications</topic><topic>Hepatitis C - drug therapy</topic><topic>Hepatitis C Antibodies - analysis</topic><topic>Hepatitis C virus</topic><topic>Hepatology</topic><topic>HIV Infections - complications</topic><topic>HIV Infections - drug therapy</topic><topic>Human immunodeficiency virus</topic><topic>Human viral diseases</topic><topic>Humans</topic><topic>Infectious diseases</topic><topic>Interferon-alpha - therapeutic use</topic><topic>Lentivirus</topic><topic>Liver. Biliary tract. Portal circulation. Exocrine pancreas</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Polyethylene Glycols - therapeutic use</topic><topic>Recombinant Proteins</topic><topic>Retrospective Studies</topic><topic>Retroviridae</topic><topic>Viral diseases</topic><topic>Viral diseases of the lymphoid tissue and the blood. 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In this study, the clinical, biological, and therapeutic data of 53 human immunodeficiency virus (HIV)‐infected MSM included in a multicenter prospective study on acute hepatitis C in 2006‐2007 were retrospectively collected and analyzed. The mean hepatitis C virus (HCV) viral load at diagnosis was 5.8 ± 1.1 log10 IU/mL (genotype 4, n = 28; genotype 1, n = 14, genotype 3, n = 7). The cumulative rates of spontaneous HCV clearance were 11.0% and 16.5% 3 and 6 months after diagnosis, respectively. Forty patients were treated, 38 of whom received pegylated interferon and ribavirin. The mean duration of HCV therapy was 39 ± 17 weeks (24 ± 4 weeks in 14 cases). On treatment, 18/36 (50.0%; 95% confidence interval 34.3‐65.7) patients had undetectable HCV RNA at week 4 (RVR), and 32/39 (82.1%; 95 confidence interval 70.0‐94.1) achieved sustained virological response (SVR). SVR did not correlate with pretreatment parameters, including HCV genotype, but correlated with RVR (predictive positive value of 94.4%) and with effective duration of HCV therapy (64.3% for 24 ± 4 weeks versus 92.0% for longer treatment; P = 0.03). Conclusion: The low rate of spontaneous clearance and the high SVR rates argue for early HCV therapy following diagnosis of acute hepatitis C in HIV‐infected MSM. Pegylated interferon and ribavirin seem to be the best option. The duration of treatment should be modulated according to RVR, with a 24‐week course for patients presenting RVR and a 48‐week course for those who do not, irrespectively of HCV genotype. (HEPATOLOGY 2010)</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>21064156</pmid><doi>10.1002/hep.23959</doi><tpages>7</tpages></addata></record> |
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subjects | Acute Disease Adult Antiviral Agents - therapeutic use Biological and medical sciences Gastroenterology. Liver. Pancreas. Abdomen Hepatitis C Hepatitis C - complications Hepatitis C - drug therapy Hepatitis C Antibodies - analysis Hepatitis C virus Hepatology HIV Infections - complications HIV Infections - drug therapy Human immunodeficiency virus Human viral diseases Humans Infectious diseases Interferon-alpha - therapeutic use Lentivirus Liver. Biliary tract. Portal circulation. Exocrine pancreas Male Medical sciences Middle Aged Polyethylene Glycols - therapeutic use Recombinant Proteins Retrospective Studies Retroviridae Viral diseases Viral diseases of the lymphoid tissue and the blood. Aids Viral hepatitis Viral Load - drug effects |
title | Treatment of acute hepatitis C in human immunodeficiency virus–infected patients: The HEPAIG study |
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