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
Hauptverfasser: 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
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container_end_page 15
container_issue 1
container_start_page 9
container_title Internal Medicine
container_volume 51
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 &amp; 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 &amp; dosage ; Male ; Middle Aged ; pegylated interferon ; Polyethylene Glycols - administration &amp; dosage ; rapid virological response ; Recombinant Proteins - administration &amp; dosage ; ribavirin ; Ribavirin - administration &amp; 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. 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dosage</subject><subject>ribavirin</subject><subject>Ribavirin - administration &amp; 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 ; 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dosage</topic><topic>Male</topic><topic>Middle Aged</topic><topic>pegylated interferon</topic><topic>Polyethylene Glycols - administration &amp; dosage</topic><topic>rapid virological response</topic><topic>Recombinant Proteins - administration &amp; dosage</topic><topic>ribavirin</topic><topic>Ribavirin - administration &amp; 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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identifier ISSN: 0918-2918
ispartof Internal Medicine, 2012, Vol.51(1), pp.9-15
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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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