A Multicenter Study to Clarify the Optimal HCV-RNA Negative Period during Combined Therapy with Pegylated Interferon Plus Ribavirin in Patients with Chronic Hepatitis Caused by HCV Genotype 2
Objective A multicenter open trial was performed to clarify the optimal duration of combined pegylated interferon (Peg-IFN) plus ribavirin therapy in patients with chronic hepatitis caused by HCV genotype 2. Methods A total of 100 patients seen between 2005 and 2007 received the combination therapy...
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Veröffentlicht in: | Internal Medicine 2012, Vol.51(1), pp.9-15 |
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creator | Nagoshi, Sumiko Koshima, Yohei Nakamura, Ikuo Funyu, Junji Sekine, Chuichi Harada, Youji Nishikawa, Ko Yoshida, Takeshi Matsui, Atsushi Sotome, Naoki Toshima, Kenichi Takegoshi, So Shiomi, Masao Tanaka, Masahiko Saito, Akira Fujiwara, Kenji Mochida, Satoshi |
description | Objective A multicenter open trial was performed to clarify the optimal duration of combined pegylated interferon (Peg-IFN) plus ribavirin therapy in patients with chronic hepatitis caused by HCV genotype 2. Methods A total of 100 patients seen between 2005 and 2007 received the combination therapy for 4 to 52 weeks. The cutoff value of the HCV-RNA-negative (titers under 1.7 Log IU/mL) period during the therapy to predict sustained virological response (SVR) was determined by ROC curve and multivariate logistic regression analyses. The result was validated in 48 patients between 2008 and 2009. Results SVR was achieved in 78 patients. Serum HCV-RNA titers decreased to less than 1.7 Log IU/mL at 4 weeks of the therapy in 60 patients. The SVR rate in these patients was 85%, which was significantly higher than that of remaining 40 patients with a SVR rate of 68%. An HCV-RNA-negative period of ≥17 weeks was selected as the cutoff value, which showed a significant odds ratio of 4.77 for SVR. Among the 35 patients who showed a decrease of the serum HCV-RNA of less than 1.7 Log IU/mL between 8 and 16 weeks of therapy, the SVR rate was significantly higher in 16 patients with a serum HCV-RNA-negative period of ≥17 weeks (94%) than in 19 patients in whom the period was less than 17 weeks (63%). Similar results were obtained in the subsequent validation study. Conclusion Prolonged combined Peg-IFN plus ribavirin therapy, with an HCV-RNA-negative period of ≥17 weeks, yielded good therapeutic outcomes in patients with chronic HCV genotype 2 hepatitis. |
doi_str_mv | 10.2169/internalmedicine.51.6237 |
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Methods A total of 100 patients seen between 2005 and 2007 received the combination therapy for 4 to 52 weeks. The cutoff value of the HCV-RNA-negative (titers under 1.7 Log IU/mL) period during the therapy to predict sustained virological response (SVR) was determined by ROC curve and multivariate logistic regression analyses. The result was validated in 48 patients between 2008 and 2009. Results SVR was achieved in 78 patients. Serum HCV-RNA titers decreased to less than 1.7 Log IU/mL at 4 weeks of the therapy in 60 patients. The SVR rate in these patients was 85%, which was significantly higher than that of remaining 40 patients with a SVR rate of 68%. An HCV-RNA-negative period of ≥17 weeks was selected as the cutoff value, which showed a significant odds ratio of 4.77 for SVR. Among the 35 patients who showed a decrease of the serum HCV-RNA of less than 1.7 Log IU/mL between 8 and 16 weeks of therapy, the SVR rate was significantly higher in 16 patients with a serum HCV-RNA-negative period of ≥17 weeks (94%) than in 19 patients in whom the period was less than 17 weeks (63%). Similar results were obtained in the subsequent validation study. Conclusion Prolonged combined Peg-IFN plus ribavirin therapy, with an HCV-RNA-negative period of ≥17 weeks, yielded good therapeutic outcomes in patients with chronic HCV genotype 2 hepatitis.</description><identifier>ISSN: 0918-2918</identifier><identifier>EISSN: 1349-7235</identifier><identifier>DOI: 10.2169/internalmedicine.51.6237</identifier><identifier>PMID: 22214617</identifier><language>eng</language><publisher>Japan: The Japanese Society of Internal Medicine</publisher><subject>Adult ; Aged ; Antiviral Agents - administration & dosage ; chronic hepatitis ; Cohort Studies ; Female ; Genotype ; genotype 2 ; HCV ; Hepacivirus - classification ; Hepacivirus - genetics ; Hepatitis C, Chronic - drug therapy ; Hepatitis C, Chronic - virology ; Humans ; Interferon alpha-2 ; Interferon-alpha - administration & dosage ; Male ; Middle Aged ; pegylated interferon ; Polyethylene Glycols - administration & dosage ; rapid virological response ; Recombinant Proteins - administration & dosage ; ribavirin ; Ribavirin - administration & dosage ; RNA, Viral - blood ; sustained virological response ; Treatment Outcome</subject><ispartof>Internal Medicine, 2012, Vol.51(1), pp.9-15</ispartof><rights>2012 by The Japanese Society of Internal Medicine</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c521t-64b263ad07631510dda8200e2fcff41091176e34fdcc1289d7eb4f2661dec5543</citedby><cites>FETCH-LOGICAL-c521t-64b263ad07631510dda8200e2fcff41091176e34fdcc1289d7eb4f2661dec5543</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,1877,4010,27900,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22214617$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Nagoshi, Sumiko</creatorcontrib><creatorcontrib>Koshima, Yohei</creatorcontrib><creatorcontrib>Nakamura, Ikuo</creatorcontrib><creatorcontrib>Funyu, Junji</creatorcontrib><creatorcontrib>Sekine, Chuichi</creatorcontrib><creatorcontrib>Harada, Youji</creatorcontrib><creatorcontrib>Nishikawa, Ko</creatorcontrib><creatorcontrib>Yoshida, Takeshi</creatorcontrib><creatorcontrib>Matsui, Atsushi</creatorcontrib><creatorcontrib>Sotome, Naoki</creatorcontrib><creatorcontrib>Toshima, Kenichi</creatorcontrib><creatorcontrib>Takegoshi, So</creatorcontrib><creatorcontrib>Shiomi, Masao</creatorcontrib><creatorcontrib>Tanaka, Masahiko</creatorcontrib><creatorcontrib>Saito, Akira</creatorcontrib><creatorcontrib>Fujiwara, Kenji</creatorcontrib><creatorcontrib>Mochida, Satoshi</creatorcontrib><title>A Multicenter Study to Clarify the Optimal HCV-RNA Negative Period during Combined Therapy with Pegylated Interferon Plus Ribavirin in Patients with Chronic Hepatitis Caused by HCV Genotype 2</title><title>Internal Medicine</title><addtitle>Intern. Med.</addtitle><description>Objective A multicenter open trial was performed to clarify the optimal duration of combined pegylated interferon (Peg-IFN) plus ribavirin therapy in patients with chronic hepatitis caused by HCV genotype 2. Methods A total of 100 patients seen between 2005 and 2007 received the combination therapy for 4 to 52 weeks. The cutoff value of the HCV-RNA-negative (titers under 1.7 Log IU/mL) period during the therapy to predict sustained virological response (SVR) was determined by ROC curve and multivariate logistic regression analyses. The result was validated in 48 patients between 2008 and 2009. Results SVR was achieved in 78 patients. Serum HCV-RNA titers decreased to less than 1.7 Log IU/mL at 4 weeks of the therapy in 60 patients. The SVR rate in these patients was 85%, which was significantly higher than that of remaining 40 patients with a SVR rate of 68%. An HCV-RNA-negative period of ≥17 weeks was selected as the cutoff value, which showed a significant odds ratio of 4.77 for SVR. Among the 35 patients who showed a decrease of the serum HCV-RNA of less than 1.7 Log IU/mL between 8 and 16 weeks of therapy, the SVR rate was significantly higher in 16 patients with a serum HCV-RNA-negative period of ≥17 weeks (94%) than in 19 patients in whom the period was less than 17 weeks (63%). Similar results were obtained in the subsequent validation study. Conclusion Prolonged combined Peg-IFN plus ribavirin therapy, with an HCV-RNA-negative period of ≥17 weeks, yielded good therapeutic outcomes in patients with chronic HCV genotype 2 hepatitis.</description><subject>Adult</subject><subject>Aged</subject><subject>Antiviral Agents - administration & dosage</subject><subject>chronic hepatitis</subject><subject>Cohort Studies</subject><subject>Female</subject><subject>Genotype</subject><subject>genotype 2</subject><subject>HCV</subject><subject>Hepacivirus - classification</subject><subject>Hepacivirus - genetics</subject><subject>Hepatitis C, Chronic - drug therapy</subject><subject>Hepatitis C, Chronic - virology</subject><subject>Humans</subject><subject>Interferon alpha-2</subject><subject>Interferon-alpha - administration & dosage</subject><subject>Male</subject><subject>Middle Aged</subject><subject>pegylated interferon</subject><subject>Polyethylene Glycols - administration & dosage</subject><subject>rapid virological response</subject><subject>Recombinant Proteins - administration & dosage</subject><subject>ribavirin</subject><subject>Ribavirin - administration & dosage</subject><subject>RNA, Viral - blood</subject><subject>sustained virological response</subject><subject>Treatment Outcome</subject><issn>0918-2918</issn><issn>1349-7235</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNptkdtu1DAQhiMEokvhFdDccZXFhxwvVxF0i0q7KoXbyLEnG1feJNhOUZ6OV8NRyl4gJGtsjb_5ZzR_FAElW0az8qPuPdpemBMqLXWP25RuM8bzF9GG8qSMc8bTl9GGlLSIWQgX0RvnHgnhRV6y19EFY4wmGc030e8dfJ2M1xIXSfjmJzWDH6Aywuo2PDuEu9HrkzCwr37E97c7uMWj8PoJ4YBWDwrUZHV_hGo4NWEWBQ8dWjHO8Ev7LjDH2Qgf0tdLhxbt0MPBTA7udSOedCiFcA5BMYzg1qKqC5SWsMcx5L12UInJBY1mXqaAK-wHP48I7G30qhXG4bvn-zL6_vnTQ7WPb-6urqvdTSxTRn2cJQ3LuFAkzzhNKVFKFIwQZK1s24SGRdE8Q560SkrKilLl2CQtyzKqUKZpwi-jD6vuaIefEzpfn7STaIzocZhcXdKEE0LzPJDFSko7OGexrUcb1mfnmpJ6ca_-1706pfXiXih9_9xkasLnufCvXQH4sgKPzosjngFhg4MG_6tM11CeIdkJW2PP_wC1JLnq</recordid><startdate>2012</startdate><enddate>2012</enddate><creator>Nagoshi, Sumiko</creator><creator>Koshima, Yohei</creator><creator>Nakamura, Ikuo</creator><creator>Funyu, Junji</creator><creator>Sekine, Chuichi</creator><creator>Harada, Youji</creator><creator>Nishikawa, Ko</creator><creator>Yoshida, Takeshi</creator><creator>Matsui, Atsushi</creator><creator>Sotome, Naoki</creator><creator>Toshima, Kenichi</creator><creator>Takegoshi, So</creator><creator>Shiomi, Masao</creator><creator>Tanaka, Masahiko</creator><creator>Saito, Akira</creator><creator>Fujiwara, Kenji</creator><creator>Mochida, Satoshi</creator><general>The Japanese Society of Internal Medicine</general><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>7X8</scope></search><sort><creationdate>2012</creationdate><title>A Multicenter Study to Clarify the Optimal HCV-RNA Negative Period during Combined Therapy with Pegylated Interferon Plus Ribavirin in Patients with Chronic Hepatitis Caused by HCV Genotype 2</title><author>Nagoshi, Sumiko ; Koshima, Yohei ; Nakamura, Ikuo ; Funyu, Junji ; Sekine, Chuichi ; Harada, Youji ; Nishikawa, Ko ; Yoshida, Takeshi ; Matsui, Atsushi ; Sotome, Naoki ; Toshima, Kenichi ; Takegoshi, So ; Shiomi, Masao ; Tanaka, Masahiko ; Saito, Akira ; Fujiwara, Kenji ; Mochida, Satoshi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c521t-64b263ad07631510dda8200e2fcff41091176e34fdcc1289d7eb4f2661dec5543</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Antiviral Agents - administration & dosage</topic><topic>chronic hepatitis</topic><topic>Cohort Studies</topic><topic>Female</topic><topic>Genotype</topic><topic>genotype 2</topic><topic>HCV</topic><topic>Hepacivirus - classification</topic><topic>Hepacivirus - genetics</topic><topic>Hepatitis C, Chronic - drug therapy</topic><topic>Hepatitis C, Chronic - virology</topic><topic>Humans</topic><topic>Interferon alpha-2</topic><topic>Interferon-alpha - administration & dosage</topic><topic>Male</topic><topic>Middle Aged</topic><topic>pegylated interferon</topic><topic>Polyethylene Glycols - administration & dosage</topic><topic>rapid virological response</topic><topic>Recombinant Proteins - administration & dosage</topic><topic>ribavirin</topic><topic>Ribavirin - administration & dosage</topic><topic>RNA, Viral - blood</topic><topic>sustained virological response</topic><topic>Treatment Outcome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Nagoshi, Sumiko</creatorcontrib><creatorcontrib>Koshima, Yohei</creatorcontrib><creatorcontrib>Nakamura, Ikuo</creatorcontrib><creatorcontrib>Funyu, Junji</creatorcontrib><creatorcontrib>Sekine, Chuichi</creatorcontrib><creatorcontrib>Harada, Youji</creatorcontrib><creatorcontrib>Nishikawa, Ko</creatorcontrib><creatorcontrib>Yoshida, Takeshi</creatorcontrib><creatorcontrib>Matsui, Atsushi</creatorcontrib><creatorcontrib>Sotome, Naoki</creatorcontrib><creatorcontrib>Toshima, Kenichi</creatorcontrib><creatorcontrib>Takegoshi, So</creatorcontrib><creatorcontrib>Shiomi, Masao</creatorcontrib><creatorcontrib>Tanaka, Masahiko</creatorcontrib><creatorcontrib>Saito, Akira</creatorcontrib><creatorcontrib>Fujiwara, Kenji</creatorcontrib><creatorcontrib>Mochida, Satoshi</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Internal Medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Nagoshi, Sumiko</au><au>Koshima, Yohei</au><au>Nakamura, Ikuo</au><au>Funyu, Junji</au><au>Sekine, Chuichi</au><au>Harada, Youji</au><au>Nishikawa, Ko</au><au>Yoshida, Takeshi</au><au>Matsui, Atsushi</au><au>Sotome, Naoki</au><au>Toshima, Kenichi</au><au>Takegoshi, So</au><au>Shiomi, Masao</au><au>Tanaka, Masahiko</au><au>Saito, Akira</au><au>Fujiwara, Kenji</au><au>Mochida, Satoshi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A Multicenter Study to Clarify the Optimal HCV-RNA Negative Period during Combined Therapy with Pegylated Interferon Plus Ribavirin in Patients with Chronic Hepatitis Caused by HCV Genotype 2</atitle><jtitle>Internal Medicine</jtitle><addtitle>Intern. Med.</addtitle><date>2012</date><risdate>2012</risdate><volume>51</volume><issue>1</issue><spage>9</spage><epage>15</epage><pages>9-15</pages><issn>0918-2918</issn><eissn>1349-7235</eissn><abstract>Objective A multicenter open trial was performed to clarify the optimal duration of combined pegylated interferon (Peg-IFN) plus ribavirin therapy in patients with chronic hepatitis caused by HCV genotype 2. Methods A total of 100 patients seen between 2005 and 2007 received the combination therapy for 4 to 52 weeks. The cutoff value of the HCV-RNA-negative (titers under 1.7 Log IU/mL) period during the therapy to predict sustained virological response (SVR) was determined by ROC curve and multivariate logistic regression analyses. The result was validated in 48 patients between 2008 and 2009. Results SVR was achieved in 78 patients. Serum HCV-RNA titers decreased to less than 1.7 Log IU/mL at 4 weeks of the therapy in 60 patients. The SVR rate in these patients was 85%, which was significantly higher than that of remaining 40 patients with a SVR rate of 68%. An HCV-RNA-negative period of ≥17 weeks was selected as the cutoff value, which showed a significant odds ratio of 4.77 for SVR. Among the 35 patients who showed a decrease of the serum HCV-RNA of less than 1.7 Log IU/mL between 8 and 16 weeks of therapy, the SVR rate was significantly higher in 16 patients with a serum HCV-RNA-negative period of ≥17 weeks (94%) than in 19 patients in whom the period was less than 17 weeks (63%). Similar results were obtained in the subsequent validation study. Conclusion Prolonged combined Peg-IFN plus ribavirin therapy, with an HCV-RNA-negative period of ≥17 weeks, yielded good therapeutic outcomes in patients with chronic HCV genotype 2 hepatitis.</abstract><cop>Japan</cop><pub>The Japanese Society of Internal Medicine</pub><pmid>22214617</pmid><doi>10.2169/internalmedicine.51.6237</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adult Aged Antiviral Agents - administration & dosage chronic hepatitis Cohort Studies Female Genotype genotype 2 HCV Hepacivirus - classification Hepacivirus - genetics Hepatitis C, Chronic - drug therapy Hepatitis C, Chronic - virology Humans Interferon alpha-2 Interferon-alpha - administration & dosage Male Middle Aged pegylated interferon Polyethylene Glycols - administration & dosage rapid virological response Recombinant Proteins - administration & dosage ribavirin Ribavirin - administration & dosage RNA, Viral - blood sustained virological response Treatment Outcome |
title | A Multicenter Study to Clarify the Optimal HCV-RNA Negative Period during Combined Therapy with Pegylated Interferon Plus Ribavirin in Patients with Chronic Hepatitis Caused by HCV Genotype 2 |
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