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Multicenter comparison of PEG-IFN α2a or α2b plus ribavirin for treatment-naïve HCV patient in Korean population
Two recent Italian studies suggested that Pegylated-interferon (PEG-IFN) alfa-2a achieves a higher sustained virological response (SVR) rate than PEG-IFN alfa-2b. We intended to compare the efficacy and safety of PEG-IFN alfa-2a with those of PEG-IFN alfa-2b in Korean patients with chronic hepatitis...
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Published in: | BMC gastroenterology 2013-04, Vol.13 (1), p.74-74, Article 74 |
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creator | Jin, Young-Joo Lee, Jin-Woo Lee, Jung Il Park, Sang Hoon Park, Choong Kee Kim, Young Seok Jeong, Sook-Hyang Kim, Yun Soo Kim, Ju Hyun Hwang, Seong Gyu Rim, Kyu Sung Yim, Hyung Joon Cheong, Jae Youn Cho, Sung Won Lee, June Sung Park, Young Min Jang, Jeong Won Lee, Chun Kyon Sohn, Joo Hyun Yang, Jin Mo Han, Seungbong |
description | Two recent Italian studies suggested that Pegylated-interferon (PEG-IFN) alfa-2a achieves a higher sustained virological response (SVR) rate than PEG-IFN alfa-2b. We intended to compare the efficacy and safety of PEG-IFN alfa-2a with those of PEG-IFN alfa-2b in Korean patients with chronic hepatitis C virus (HCV).
This retrospective, multi-center trial was conducted on 661 treatment-naïve chronic HCV patients. Patients received PEG-IFN alfa-2a (180 μg/week; n=402) or PEG-IFN alfa-2b (1.5 μg/kg/week; n=259) with ribavirin (800-1200 mg/day) for 24 or 48 weeks according to HCV genotypes.
Early virologic response and sustained virologic response (SVR) rates were not significantly different between two PEG-IFN groups both in patients with HCV genotype 1 (all P-values>0.05) and 2/3 (all P-values>0.05). SVR rates were not different between two groups in each categorized baseline characteristics: age (years) (≤ 50 and >50), HCV viral load (IU/mL) (≤ 7 × 10(5) and >7 × 10(5)), and hepatic fibrosis (F0-2 and F3-4) (all P-values >0.05). In additional analysis for 480 patients who sufficiently complied with treatment doses and duration (80/80/80 rule) and propensity-score matched analysis, SVR rates were not different between two groups both in patients with HCV genotype 1 and 2/3 (all P-values >0.05). Adverse event rates were similar between two groups.
Unlike the Western data, efficacy and safety of PEG-IFN alfa-2a were similar to those of PEG-IFN alfa-2b in chronically HCV-infected Korean patients regardless of age, HCV viral load, and hepatic fibrosis. |
doi_str_mv | 10.1186/1471-230X-13-74 |
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This retrospective, multi-center trial was conducted on 661 treatment-naïve chronic HCV patients. Patients received PEG-IFN alfa-2a (180 μg/week; n=402) or PEG-IFN alfa-2b (1.5 μg/kg/week; n=259) with ribavirin (800-1200 mg/day) for 24 or 48 weeks according to HCV genotypes.
Early virologic response and sustained virologic response (SVR) rates were not significantly different between two PEG-IFN groups both in patients with HCV genotype 1 (all P-values>0.05) and 2/3 (all P-values>0.05). SVR rates were not different between two groups in each categorized baseline characteristics: age (years) (≤ 50 and >50), HCV viral load (IU/mL) (≤ 7 × 10(5) and >7 × 10(5)), and hepatic fibrosis (F0-2 and F3-4) (all P-values >0.05). In additional analysis for 480 patients who sufficiently complied with treatment doses and duration (80/80/80 rule) and propensity-score matched analysis, SVR rates were not different between two groups both in patients with HCV genotype 1 and 2/3 (all P-values >0.05). Adverse event rates were similar between two groups.
Unlike the Western data, efficacy and safety of PEG-IFN alfa-2a were similar to those of PEG-IFN alfa-2b in chronically HCV-infected Korean patients regardless of age, HCV viral load, and hepatic fibrosis.</description><identifier>ISSN: 1471-230X</identifier><identifier>EISSN: 1471-230X</identifier><identifier>DOI: 10.1186/1471-230X-13-74</identifier><identifier>PMID: 23627926</identifier><language>eng</language><publisher>England: BioMed Central Ltd</publisher><subject>Antiviral Agents - adverse effects ; Antiviral Agents - therapeutic use ; Drug Therapy, Combination ; Female ; Hepacivirus - genetics ; Hepatitis C, Chronic - drug therapy ; Hepatitis C, Chronic - virology ; Humans ; Interferon-alpha - adverse effects ; Interferon-alpha - therapeutic use ; Male ; Middle Aged ; Polyethylene Glycols - adverse effects ; Polyethylene Glycols - therapeutic use ; Recombinant Proteins - adverse effects ; Recombinant Proteins - therapeutic use ; Republic of Korea ; Retrospective Studies ; Ribavirin - therapeutic use ; Viral Load</subject><ispartof>BMC gastroenterology, 2013-04, Vol.13 (1), p.74-74, Article 74</ispartof><rights>Copyright © 2013 Jin et al.; licensee BioMed Central Ltd. 2013 Jin et al.; licensee BioMed Central Ltd.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b3674-6999ef77d19a09bd6e65f7838ef1a251d8b41370b875ea17dd91b8c690321b7c3</citedby><cites>FETCH-LOGICAL-b3674-6999ef77d19a09bd6e65f7838ef1a251d8b41370b875ea17dd91b8c690321b7c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3644280/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3644280/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27898,27899,53763,53765</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23627926$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Jin, Young-Joo</creatorcontrib><creatorcontrib>Lee, Jin-Woo</creatorcontrib><creatorcontrib>Lee, Jung Il</creatorcontrib><creatorcontrib>Park, Sang Hoon</creatorcontrib><creatorcontrib>Park, Choong Kee</creatorcontrib><creatorcontrib>Kim, Young Seok</creatorcontrib><creatorcontrib>Jeong, Sook-Hyang</creatorcontrib><creatorcontrib>Kim, Yun Soo</creatorcontrib><creatorcontrib>Kim, Ju Hyun</creatorcontrib><creatorcontrib>Hwang, Seong Gyu</creatorcontrib><creatorcontrib>Rim, Kyu Sung</creatorcontrib><creatorcontrib>Yim, Hyung Joon</creatorcontrib><creatorcontrib>Cheong, Jae Youn</creatorcontrib><creatorcontrib>Cho, Sung Won</creatorcontrib><creatorcontrib>Lee, June Sung</creatorcontrib><creatorcontrib>Park, Young Min</creatorcontrib><creatorcontrib>Jang, Jeong Won</creatorcontrib><creatorcontrib>Lee, Chun Kyon</creatorcontrib><creatorcontrib>Sohn, Joo Hyun</creatorcontrib><creatorcontrib>Yang, Jin Mo</creatorcontrib><creatorcontrib>Han, Seungbong</creatorcontrib><title>Multicenter comparison of PEG-IFN α2a or α2b plus ribavirin for treatment-naïve HCV patient in Korean population</title><title>BMC gastroenterology</title><addtitle>BMC Gastroenterol</addtitle><description>Two recent Italian studies suggested that Pegylated-interferon (PEG-IFN) alfa-2a achieves a higher sustained virological response (SVR) rate than PEG-IFN alfa-2b. We intended to compare the efficacy and safety of PEG-IFN alfa-2a with those of PEG-IFN alfa-2b in Korean patients with chronic hepatitis C virus (HCV).
This retrospective, multi-center trial was conducted on 661 treatment-naïve chronic HCV patients. Patients received PEG-IFN alfa-2a (180 μg/week; n=402) or PEG-IFN alfa-2b (1.5 μg/kg/week; n=259) with ribavirin (800-1200 mg/day) for 24 or 48 weeks according to HCV genotypes.
Early virologic response and sustained virologic response (SVR) rates were not significantly different between two PEG-IFN groups both in patients with HCV genotype 1 (all P-values>0.05) and 2/3 (all P-values>0.05). SVR rates were not different between two groups in each categorized baseline characteristics: age (years) (≤ 50 and >50), HCV viral load (IU/mL) (≤ 7 × 10(5) and >7 × 10(5)), and hepatic fibrosis (F0-2 and F3-4) (all P-values >0.05). In additional analysis for 480 patients who sufficiently complied with treatment doses and duration (80/80/80 rule) and propensity-score matched analysis, SVR rates were not different between two groups both in patients with HCV genotype 1 and 2/3 (all P-values >0.05). Adverse event rates were similar between two groups.
Unlike the Western data, efficacy and safety of PEG-IFN alfa-2a were similar to those of PEG-IFN alfa-2b in chronically HCV-infected Korean patients regardless of age, HCV viral load, and hepatic fibrosis.</description><subject>Antiviral Agents - adverse effects</subject><subject>Antiviral Agents - therapeutic use</subject><subject>Drug Therapy, Combination</subject><subject>Female</subject><subject>Hepacivirus - genetics</subject><subject>Hepatitis C, Chronic - drug therapy</subject><subject>Hepatitis C, Chronic - virology</subject><subject>Humans</subject><subject>Interferon-alpha - adverse effects</subject><subject>Interferon-alpha - therapeutic use</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Polyethylene Glycols - adverse effects</subject><subject>Polyethylene Glycols - therapeutic use</subject><subject>Recombinant Proteins - adverse effects</subject><subject>Recombinant Proteins - therapeutic use</subject><subject>Republic of Korea</subject><subject>Retrospective Studies</subject><subject>Ribavirin - therapeutic use</subject><subject>Viral Load</subject><issn>1471-230X</issn><issn>1471-230X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><recordid>eNp1kctOwzAQRS0EolBYs0P-gVA_UjvZIEHVlyiPBSB2lp04YJTEkZNU4qsQ38Ceb8JRoWolWI11587R-A4AJxidYRyxAQ45DghFTwGmAQ93wMFa2d1498BhXb8ihHlE6D7oEcoIjwk7APV1mzcm0WWjHUxsUUlnaltCm8G78TSYT27g1weR0LquKljlbQ2dUXJpnClh5vXGadkUnhCU8vN9qeFs9Agr2RgvQe-5st5QwspWbe5VWx6BvUzmtT7-qX3wMBnfj2bB4nY6H10sAkUZDwMWx7HOOE9xLFGsUqbZMOMRjXSGJRniNFIhphypiA-1xDxNY6yihMWIEqx4QvvgfMWtWlXotPukk7monCmkexNWGrHdKc2LeLZLQVkYkgh5wOUKoIz9B7Dd8QGKLnTRhS4wFTz0kMEKkjhb105n63mMRHfEPyZON_de-3-vRr8BPMCcHg</recordid><startdate>20130429</startdate><enddate>20130429</enddate><creator>Jin, Young-Joo</creator><creator>Lee, Jin-Woo</creator><creator>Lee, Jung Il</creator><creator>Park, Sang Hoon</creator><creator>Park, Choong Kee</creator><creator>Kim, Young Seok</creator><creator>Jeong, Sook-Hyang</creator><creator>Kim, Yun Soo</creator><creator>Kim, Ju Hyun</creator><creator>Hwang, Seong Gyu</creator><creator>Rim, Kyu Sung</creator><creator>Yim, Hyung Joon</creator><creator>Cheong, Jae Youn</creator><creator>Cho, Sung Won</creator><creator>Lee, June Sung</creator><creator>Park, Young Min</creator><creator>Jang, Jeong Won</creator><creator>Lee, Chun Kyon</creator><creator>Sohn, Joo Hyun</creator><creator>Yang, Jin Mo</creator><creator>Han, Seungbong</creator><general>BioMed Central Ltd</general><general>BioMed Central</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>5PM</scope></search><sort><creationdate>20130429</creationdate><title>Multicenter comparison of PEG-IFN α2a or α2b plus ribavirin for treatment-naïve HCV patient in Korean population</title><author>Jin, Young-Joo ; Lee, Jin-Woo ; Lee, Jung Il ; Park, Sang Hoon ; Park, Choong Kee ; Kim, Young Seok ; Jeong, Sook-Hyang ; Kim, Yun Soo ; Kim, Ju Hyun ; Hwang, Seong Gyu ; Rim, Kyu Sung ; Yim, Hyung Joon ; Cheong, Jae Youn ; Cho, Sung Won ; Lee, June Sung ; Park, Young Min ; Jang, Jeong Won ; Lee, Chun Kyon ; Sohn, Joo Hyun ; Yang, Jin Mo ; Han, Seungbong</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b3674-6999ef77d19a09bd6e65f7838ef1a251d8b41370b875ea17dd91b8c690321b7c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Antiviral Agents - adverse effects</topic><topic>Antiviral Agents - therapeutic use</topic><topic>Drug Therapy, Combination</topic><topic>Female</topic><topic>Hepacivirus - genetics</topic><topic>Hepatitis C, Chronic - drug therapy</topic><topic>Hepatitis C, Chronic - virology</topic><topic>Humans</topic><topic>Interferon-alpha - adverse effects</topic><topic>Interferon-alpha - therapeutic use</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Polyethylene Glycols - adverse effects</topic><topic>Polyethylene Glycols - therapeutic use</topic><topic>Recombinant Proteins - adverse effects</topic><topic>Recombinant Proteins - therapeutic use</topic><topic>Republic of Korea</topic><topic>Retrospective Studies</topic><topic>Ribavirin - therapeutic use</topic><topic>Viral Load</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jin, Young-Joo</creatorcontrib><creatorcontrib>Lee, Jin-Woo</creatorcontrib><creatorcontrib>Lee, Jung Il</creatorcontrib><creatorcontrib>Park, Sang Hoon</creatorcontrib><creatorcontrib>Park, Choong Kee</creatorcontrib><creatorcontrib>Kim, Young Seok</creatorcontrib><creatorcontrib>Jeong, Sook-Hyang</creatorcontrib><creatorcontrib>Kim, Yun Soo</creatorcontrib><creatorcontrib>Kim, Ju Hyun</creatorcontrib><creatorcontrib>Hwang, Seong Gyu</creatorcontrib><creatorcontrib>Rim, Kyu Sung</creatorcontrib><creatorcontrib>Yim, Hyung Joon</creatorcontrib><creatorcontrib>Cheong, Jae Youn</creatorcontrib><creatorcontrib>Cho, Sung Won</creatorcontrib><creatorcontrib>Lee, June Sung</creatorcontrib><creatorcontrib>Park, Young Min</creatorcontrib><creatorcontrib>Jang, Jeong Won</creatorcontrib><creatorcontrib>Lee, Chun Kyon</creatorcontrib><creatorcontrib>Sohn, Joo Hyun</creatorcontrib><creatorcontrib>Yang, Jin Mo</creatorcontrib><creatorcontrib>Han, Seungbong</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>BMC gastroenterology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jin, Young-Joo</au><au>Lee, Jin-Woo</au><au>Lee, Jung Il</au><au>Park, Sang Hoon</au><au>Park, Choong Kee</au><au>Kim, Young Seok</au><au>Jeong, Sook-Hyang</au><au>Kim, Yun Soo</au><au>Kim, Ju Hyun</au><au>Hwang, Seong Gyu</au><au>Rim, Kyu Sung</au><au>Yim, Hyung Joon</au><au>Cheong, Jae Youn</au><au>Cho, Sung Won</au><au>Lee, June Sung</au><au>Park, Young Min</au><au>Jang, Jeong Won</au><au>Lee, Chun Kyon</au><au>Sohn, Joo Hyun</au><au>Yang, Jin Mo</au><au>Han, Seungbong</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Multicenter comparison of PEG-IFN α2a or α2b plus ribavirin for treatment-naïve HCV patient in Korean population</atitle><jtitle>BMC gastroenterology</jtitle><addtitle>BMC Gastroenterol</addtitle><date>2013-04-29</date><risdate>2013</risdate><volume>13</volume><issue>1</issue><spage>74</spage><epage>74</epage><pages>74-74</pages><artnum>74</artnum><issn>1471-230X</issn><eissn>1471-230X</eissn><abstract>Two recent Italian studies suggested that Pegylated-interferon (PEG-IFN) alfa-2a achieves a higher sustained virological response (SVR) rate than PEG-IFN alfa-2b. We intended to compare the efficacy and safety of PEG-IFN alfa-2a with those of PEG-IFN alfa-2b in Korean patients with chronic hepatitis C virus (HCV).
This retrospective, multi-center trial was conducted on 661 treatment-naïve chronic HCV patients. Patients received PEG-IFN alfa-2a (180 μg/week; n=402) or PEG-IFN alfa-2b (1.5 μg/kg/week; n=259) with ribavirin (800-1200 mg/day) for 24 or 48 weeks according to HCV genotypes.
Early virologic response and sustained virologic response (SVR) rates were not significantly different between two PEG-IFN groups both in patients with HCV genotype 1 (all P-values>0.05) and 2/3 (all P-values>0.05). SVR rates were not different between two groups in each categorized baseline characteristics: age (years) (≤ 50 and >50), HCV viral load (IU/mL) (≤ 7 × 10(5) and >7 × 10(5)), and hepatic fibrosis (F0-2 and F3-4) (all P-values >0.05). In additional analysis for 480 patients who sufficiently complied with treatment doses and duration (80/80/80 rule) and propensity-score matched analysis, SVR rates were not different between two groups both in patients with HCV genotype 1 and 2/3 (all P-values >0.05). Adverse event rates were similar between two groups.
Unlike the Western data, efficacy and safety of PEG-IFN alfa-2a were similar to those of PEG-IFN alfa-2b in chronically HCV-infected Korean patients regardless of age, HCV viral load, and hepatic fibrosis.</abstract><cop>England</cop><pub>BioMed Central Ltd</pub><pmid>23627926</pmid><doi>10.1186/1471-230X-13-74</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Antiviral Agents - adverse effects Antiviral Agents - therapeutic use Drug Therapy, Combination Female Hepacivirus - genetics Hepatitis C, Chronic - drug therapy Hepatitis C, Chronic - virology Humans Interferon-alpha - adverse effects Interferon-alpha - therapeutic use Male Middle Aged Polyethylene Glycols - adverse effects Polyethylene Glycols - therapeutic use Recombinant Proteins - adverse effects Recombinant Proteins - therapeutic use Republic of Korea Retrospective Studies Ribavirin - therapeutic use Viral Load |
title | Multicenter comparison of PEG-IFN α2a or α2b plus ribavirin for treatment-naïve HCV patient in Korean population |
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