Pegylated interferon alpha‐2b plus ribavirin in patients with genotype 4 chronic hepatitis C: The role of rapid and early virologic response

In patients chronically infected with hepatitis C virus (HCV) genotype 4, the optimum duration of therapy and the predictors of sustained virologic response (SVR) have not been adequately determined. In this study, 358 patients with chronic hepatitis C genotype 4 were randomly assigned to pegylated...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Hepatology (Baltimore, Md.) Md.), 2007-12, Vol.46 (6), p.1732-1740
Hauptverfasser: Kamal, Sanaa M., El Kamary, Samer S., Shardell, Michelle D., Hashem, Mohamed, Ahmed, Imad N., Muhammadi, Mohamed, Sayed, Khalifa, Moustafa, Ashraf, Hakem, Sarah Abdel, Ibrahiem, Amany, Moniem, Mohamed, Mansour, Hoda, Abdelaziz, Mohamed
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 1740
container_issue 6
container_start_page 1732
container_title Hepatology (Baltimore, Md.)
container_volume 46
creator Kamal, Sanaa M.
El Kamary, Samer S.
Shardell, Michelle D.
Hashem, Mohamed
Ahmed, Imad N.
Muhammadi, Mohamed
Sayed, Khalifa
Moustafa, Ashraf
Hakem, Sarah Abdel
Ibrahiem, Amany
Moniem, Mohamed
Mansour, Hoda
Abdelaziz, Mohamed
description In patients chronically infected with hepatitis C virus (HCV) genotype 4, the optimum duration of therapy and the predictors of sustained virologic response (SVR) have not been adequately determined. In this study, 358 patients with chronic hepatitis C genotype 4 were randomly assigned to pegylated interferon (PEG‐IFN) alpha‐2b (1.5 μg/kg/week) plus oral ribavirin (10.6 mg/kg/day) for a fixed duration of 48 weeks (control group, n = 50) or for a variable duration (n = 318). In the variable‐duration group, patients with undetectable HCV RNA at week 4 were treated for 24 weeks (group A, n = 69), patients with undetectable HCV RNA at week 12 were treated for 36 weeks (group B, n = 79), and the rest of the patients were treated for 48 weeks (group C, n = 160). The primary endpoint was SVR (undetectable HCV RNA 24 weeks after treatment cessation). Groups A‐C and the control group had SVR rates of 86%, 76%, 56%, and 58%, respectively. After the study was controlled for predictors, a low baseline histologic grade and stage were associated with SVR (P < 0.029) in all groups. In addition, among patients in group C, older age (P = 0.04), a higher baseline body mass index (P = 0.013), and low baseline HCV RNA (P < 0.001) were also associated with SVR attainment. The incidence of adverse events and the rate of discontinuation were higher in patients in the variable‐duration and fixed‐duration groups treated for 48 weeks. Conclusion: In patients with chronic hepatitis C genotype 4 and undetectable HCV RNA at weeks 4 and 12, treatment with PEG‐IFN alpha‐2b and ribavirin for 24 weeks and 36 weeks, respectively, is sufficient. (HEPATOLOGY 2007.)
doi_str_mv 10.1002/hep.21917
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_69025981</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>69025981</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3537-d2e0aa7a78255a5763e2b688a761fa41aa80a8d2e981fb7f1cfb51b3973814f73</originalsourceid><addsrcrecordid>eNp10M9u1DAQBnALUdGlcOAFkC8gcUjrP0kcc0OrliJVag_lHE2S8cbIawc72yq3PkHVZ-RJcNmVeuLky--bGX-EfODslDMmzkacTgXXXL0iK14JVUhZsddkxYRiheZSH5O3Kf1ijOlSNG_IMVe6lLrRK_J4g5vFwYwDtX7GaDAGT8FNI_x5eBIdndwu0Wg7uLPR-ozoBLNFPyd6b-eRbtCHeZmQlrQfc9b2NJ-TyWwTXX-ltyPSGBzSYGiEyQ4U_EARoltoHhlc2ORIxDQFn_AdOTLgEr4_vCfk58X57fqyuLr-_mP97aroZSVVMQhkAApUI6oKKlVLFF3dNKBqbqDkAA2DJivdcNMpw3vTVbyTWsmGl0bJE_J5P3eK4fcO09xuberROfAYdqmtNRNVDmf4ZQ_7GFKKaNop2i3EpeWsfS6_zb9t_5Wf7cfD0F23xeFFHtrO4NMBQOrBmQi-t-nFac1rJZ-Xnu3dvXW4_H9je3l-s1_9F18qnhQ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>69025981</pqid></control><display><type>article</type><title>Pegylated interferon alpha‐2b plus ribavirin in patients with genotype 4 chronic hepatitis C: The role of rapid and early virologic response</title><source>MEDLINE</source><source>EZB-FREE-00999 freely available EZB journals</source><source>Wiley Online Library All Journals</source><creator>Kamal, Sanaa M. ; El Kamary, Samer S. ; Shardell, Michelle D. ; Hashem, Mohamed ; Ahmed, Imad N. ; Muhammadi, Mohamed ; Sayed, Khalifa ; Moustafa, Ashraf ; Hakem, Sarah Abdel ; Ibrahiem, Amany ; Moniem, Mohamed ; Mansour, Hoda ; Abdelaziz, Mohamed</creator><creatorcontrib>Kamal, Sanaa M. ; El Kamary, Samer S. ; Shardell, Michelle D. ; Hashem, Mohamed ; Ahmed, Imad N. ; Muhammadi, Mohamed ; Sayed, Khalifa ; Moustafa, Ashraf ; Hakem, Sarah Abdel ; Ibrahiem, Amany ; Moniem, Mohamed ; Mansour, Hoda ; Abdelaziz, Mohamed</creatorcontrib><description>In patients chronically infected with hepatitis C virus (HCV) genotype 4, the optimum duration of therapy and the predictors of sustained virologic response (SVR) have not been adequately determined. In this study, 358 patients with chronic hepatitis C genotype 4 were randomly assigned to pegylated interferon (PEG‐IFN) alpha‐2b (1.5 μg/kg/week) plus oral ribavirin (10.6 mg/kg/day) for a fixed duration of 48 weeks (control group, n = 50) or for a variable duration (n = 318). In the variable‐duration group, patients with undetectable HCV RNA at week 4 were treated for 24 weeks (group A, n = 69), patients with undetectable HCV RNA at week 12 were treated for 36 weeks (group B, n = 79), and the rest of the patients were treated for 48 weeks (group C, n = 160). The primary endpoint was SVR (undetectable HCV RNA 24 weeks after treatment cessation). Groups A‐C and the control group had SVR rates of 86%, 76%, 56%, and 58%, respectively. After the study was controlled for predictors, a low baseline histologic grade and stage were associated with SVR (P &lt; 0.029) in all groups. In addition, among patients in group C, older age (P = 0.04), a higher baseline body mass index (P = 0.013), and low baseline HCV RNA (P &lt; 0.001) were also associated with SVR attainment. The incidence of adverse events and the rate of discontinuation were higher in patients in the variable‐duration and fixed‐duration groups treated for 48 weeks. Conclusion: In patients with chronic hepatitis C genotype 4 and undetectable HCV RNA at weeks 4 and 12, treatment with PEG‐IFN alpha‐2b and ribavirin for 24 weeks and 36 weeks, respectively, is sufficient. (HEPATOLOGY 2007.)</description><identifier>ISSN: 0270-9139</identifier><identifier>EISSN: 1527-3350</identifier><identifier>DOI: 10.1002/hep.21917</identifier><identifier>PMID: 17943989</identifier><identifier>CODEN: HPTLD9</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Adult ; Antibiotics. Antiinfectious agents. Antiparasitic agents ; Antiviral agents ; Antiviral Agents - administration &amp; dosage ; Biological and medical sciences ; Drug Administration Schedule ; Female ; Genotype ; Hepatitis C, Chronic - drug therapy ; Hepatitis C, Chronic - genetics ; Human viral diseases ; Humans ; Infectious diseases ; Interferon-alpha - administration &amp; dosage ; Male ; Medical sciences ; Middle Aged ; Pharmacology. Drug treatments ; Polyethylene Glycols ; Recombinant Proteins ; Ribavirin - administration &amp; dosage ; RNA, Viral ; Viral diseases ; Viral hepatitis ; Viral Load</subject><ispartof>Hepatology (Baltimore, Md.), 2007-12, Vol.46 (6), p.1732-1740</ispartof><rights>Copyright © 2007 American Association for the Study of Liver Diseases</rights><rights>2008 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3537-d2e0aa7a78255a5763e2b688a761fa41aa80a8d2e981fb7f1cfb51b3973814f73</citedby><cites>FETCH-LOGICAL-c3537-d2e0aa7a78255a5763e2b688a761fa41aa80a8d2e981fb7f1cfb51b3973814f73</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.21917$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fhep.21917$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27923,27924,45573,45574</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=19916731$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17943989$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kamal, Sanaa M.</creatorcontrib><creatorcontrib>El Kamary, Samer S.</creatorcontrib><creatorcontrib>Shardell, Michelle D.</creatorcontrib><creatorcontrib>Hashem, Mohamed</creatorcontrib><creatorcontrib>Ahmed, Imad N.</creatorcontrib><creatorcontrib>Muhammadi, Mohamed</creatorcontrib><creatorcontrib>Sayed, Khalifa</creatorcontrib><creatorcontrib>Moustafa, Ashraf</creatorcontrib><creatorcontrib>Hakem, Sarah Abdel</creatorcontrib><creatorcontrib>Ibrahiem, Amany</creatorcontrib><creatorcontrib>Moniem, Mohamed</creatorcontrib><creatorcontrib>Mansour, Hoda</creatorcontrib><creatorcontrib>Abdelaziz, Mohamed</creatorcontrib><title>Pegylated interferon alpha‐2b plus ribavirin in patients with genotype 4 chronic hepatitis C: The role of rapid and early virologic response</title><title>Hepatology (Baltimore, Md.)</title><addtitle>Hepatology</addtitle><description>In patients chronically infected with hepatitis C virus (HCV) genotype 4, the optimum duration of therapy and the predictors of sustained virologic response (SVR) have not been adequately determined. In this study, 358 patients with chronic hepatitis C genotype 4 were randomly assigned to pegylated interferon (PEG‐IFN) alpha‐2b (1.5 μg/kg/week) plus oral ribavirin (10.6 mg/kg/day) for a fixed duration of 48 weeks (control group, n = 50) or for a variable duration (n = 318). In the variable‐duration group, patients with undetectable HCV RNA at week 4 were treated for 24 weeks (group A, n = 69), patients with undetectable HCV RNA at week 12 were treated for 36 weeks (group B, n = 79), and the rest of the patients were treated for 48 weeks (group C, n = 160). The primary endpoint was SVR (undetectable HCV RNA 24 weeks after treatment cessation). Groups A‐C and the control group had SVR rates of 86%, 76%, 56%, and 58%, respectively. After the study was controlled for predictors, a low baseline histologic grade and stage were associated with SVR (P &lt; 0.029) in all groups. In addition, among patients in group C, older age (P = 0.04), a higher baseline body mass index (P = 0.013), and low baseline HCV RNA (P &lt; 0.001) were also associated with SVR attainment. The incidence of adverse events and the rate of discontinuation were higher in patients in the variable‐duration and fixed‐duration groups treated for 48 weeks. Conclusion: In patients with chronic hepatitis C genotype 4 and undetectable HCV RNA at weeks 4 and 12, treatment with PEG‐IFN alpha‐2b and ribavirin for 24 weeks and 36 weeks, respectively, is sufficient. (HEPATOLOGY 2007.)</description><subject>Adult</subject><subject>Antibiotics. Antiinfectious agents. Antiparasitic agents</subject><subject>Antiviral agents</subject><subject>Antiviral Agents - administration &amp; dosage</subject><subject>Biological and medical sciences</subject><subject>Drug Administration Schedule</subject><subject>Female</subject><subject>Genotype</subject><subject>Hepatitis C, Chronic - drug therapy</subject><subject>Hepatitis C, Chronic - genetics</subject><subject>Human viral diseases</subject><subject>Humans</subject><subject>Infectious diseases</subject><subject>Interferon-alpha - administration &amp; dosage</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Pharmacology. Drug treatments</subject><subject>Polyethylene Glycols</subject><subject>Recombinant Proteins</subject><subject>Ribavirin - administration &amp; dosage</subject><subject>RNA, Viral</subject><subject>Viral diseases</subject><subject>Viral hepatitis</subject><subject>Viral Load</subject><issn>0270-9139</issn><issn>1527-3350</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp10M9u1DAQBnALUdGlcOAFkC8gcUjrP0kcc0OrliJVag_lHE2S8cbIawc72yq3PkHVZ-RJcNmVeuLky--bGX-EfODslDMmzkacTgXXXL0iK14JVUhZsddkxYRiheZSH5O3Kf1ijOlSNG_IMVe6lLrRK_J4g5vFwYwDtX7GaDAGT8FNI_x5eBIdndwu0Wg7uLPR-ozoBLNFPyd6b-eRbtCHeZmQlrQfc9b2NJ-TyWwTXX-ltyPSGBzSYGiEyQ4U_EARoltoHhlc2ORIxDQFn_AdOTLgEr4_vCfk58X57fqyuLr-_mP97aroZSVVMQhkAApUI6oKKlVLFF3dNKBqbqDkAA2DJivdcNMpw3vTVbyTWsmGl0bJE_J5P3eK4fcO09xuberROfAYdqmtNRNVDmf4ZQ_7GFKKaNop2i3EpeWsfS6_zb9t_5Wf7cfD0F23xeFFHtrO4NMBQOrBmQi-t-nFac1rJZ-Xnu3dvXW4_H9je3l-s1_9F18qnhQ</recordid><startdate>200712</startdate><enddate>200712</enddate><creator>Kamal, Sanaa M.</creator><creator>El Kamary, Samer S.</creator><creator>Shardell, Michelle D.</creator><creator>Hashem, Mohamed</creator><creator>Ahmed, Imad N.</creator><creator>Muhammadi, Mohamed</creator><creator>Sayed, Khalifa</creator><creator>Moustafa, Ashraf</creator><creator>Hakem, Sarah Abdel</creator><creator>Ibrahiem, Amany</creator><creator>Moniem, Mohamed</creator><creator>Mansour, Hoda</creator><creator>Abdelaziz, Mohamed</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley</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>7X8</scope></search><sort><creationdate>200712</creationdate><title>Pegylated interferon alpha‐2b plus ribavirin in patients with genotype 4 chronic hepatitis C: The role of rapid and early virologic response</title><author>Kamal, Sanaa M. ; El Kamary, Samer S. ; Shardell, Michelle D. ; Hashem, Mohamed ; Ahmed, Imad N. ; Muhammadi, Mohamed ; Sayed, Khalifa ; Moustafa, Ashraf ; Hakem, Sarah Abdel ; Ibrahiem, Amany ; Moniem, Mohamed ; Mansour, Hoda ; Abdelaziz, Mohamed</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3537-d2e0aa7a78255a5763e2b688a761fa41aa80a8d2e981fb7f1cfb51b3973814f73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Adult</topic><topic>Antibiotics. Antiinfectious agents. Antiparasitic agents</topic><topic>Antiviral agents</topic><topic>Antiviral Agents - administration &amp; dosage</topic><topic>Biological and medical sciences</topic><topic>Drug Administration Schedule</topic><topic>Female</topic><topic>Genotype</topic><topic>Hepatitis C, Chronic - drug therapy</topic><topic>Hepatitis C, Chronic - genetics</topic><topic>Human viral diseases</topic><topic>Humans</topic><topic>Infectious diseases</topic><topic>Interferon-alpha - administration &amp; dosage</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Pharmacology. Drug treatments</topic><topic>Polyethylene Glycols</topic><topic>Recombinant Proteins</topic><topic>Ribavirin - administration &amp; dosage</topic><topic>RNA, Viral</topic><topic>Viral diseases</topic><topic>Viral hepatitis</topic><topic>Viral Load</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kamal, Sanaa M.</creatorcontrib><creatorcontrib>El Kamary, Samer S.</creatorcontrib><creatorcontrib>Shardell, Michelle D.</creatorcontrib><creatorcontrib>Hashem, Mohamed</creatorcontrib><creatorcontrib>Ahmed, Imad N.</creatorcontrib><creatorcontrib>Muhammadi, Mohamed</creatorcontrib><creatorcontrib>Sayed, Khalifa</creatorcontrib><creatorcontrib>Moustafa, Ashraf</creatorcontrib><creatorcontrib>Hakem, Sarah Abdel</creatorcontrib><creatorcontrib>Ibrahiem, Amany</creatorcontrib><creatorcontrib>Moniem, Mohamed</creatorcontrib><creatorcontrib>Mansour, Hoda</creatorcontrib><creatorcontrib>Abdelaziz, Mohamed</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>MEDLINE - Academic</collection><jtitle>Hepatology (Baltimore, Md.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kamal, Sanaa M.</au><au>El Kamary, Samer S.</au><au>Shardell, Michelle D.</au><au>Hashem, Mohamed</au><au>Ahmed, Imad N.</au><au>Muhammadi, Mohamed</au><au>Sayed, Khalifa</au><au>Moustafa, Ashraf</au><au>Hakem, Sarah Abdel</au><au>Ibrahiem, Amany</au><au>Moniem, Mohamed</au><au>Mansour, Hoda</au><au>Abdelaziz, Mohamed</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Pegylated interferon alpha‐2b plus ribavirin in patients with genotype 4 chronic hepatitis C: The role of rapid and early virologic response</atitle><jtitle>Hepatology (Baltimore, Md.)</jtitle><addtitle>Hepatology</addtitle><date>2007-12</date><risdate>2007</risdate><volume>46</volume><issue>6</issue><spage>1732</spage><epage>1740</epage><pages>1732-1740</pages><issn>0270-9139</issn><eissn>1527-3350</eissn><coden>HPTLD9</coden><abstract>In patients chronically infected with hepatitis C virus (HCV) genotype 4, the optimum duration of therapy and the predictors of sustained virologic response (SVR) have not been adequately determined. In this study, 358 patients with chronic hepatitis C genotype 4 were randomly assigned to pegylated interferon (PEG‐IFN) alpha‐2b (1.5 μg/kg/week) plus oral ribavirin (10.6 mg/kg/day) for a fixed duration of 48 weeks (control group, n = 50) or for a variable duration (n = 318). In the variable‐duration group, patients with undetectable HCV RNA at week 4 were treated for 24 weeks (group A, n = 69), patients with undetectable HCV RNA at week 12 were treated for 36 weeks (group B, n = 79), and the rest of the patients were treated for 48 weeks (group C, n = 160). The primary endpoint was SVR (undetectable HCV RNA 24 weeks after treatment cessation). Groups A‐C and the control group had SVR rates of 86%, 76%, 56%, and 58%, respectively. After the study was controlled for predictors, a low baseline histologic grade and stage were associated with SVR (P &lt; 0.029) in all groups. In addition, among patients in group C, older age (P = 0.04), a higher baseline body mass index (P = 0.013), and low baseline HCV RNA (P &lt; 0.001) were also associated with SVR attainment. The incidence of adverse events and the rate of discontinuation were higher in patients in the variable‐duration and fixed‐duration groups treated for 48 weeks. Conclusion: In patients with chronic hepatitis C genotype 4 and undetectable HCV RNA at weeks 4 and 12, treatment with PEG‐IFN alpha‐2b and ribavirin for 24 weeks and 36 weeks, respectively, is sufficient. (HEPATOLOGY 2007.)</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>17943989</pmid><doi>10.1002/hep.21917</doi><tpages>9</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0270-9139
ispartof Hepatology (Baltimore, Md.), 2007-12, Vol.46 (6), p.1732-1740
issn 0270-9139
1527-3350
language eng
recordid cdi_proquest_miscellaneous_69025981
source MEDLINE; EZB-FREE-00999 freely available EZB journals; Wiley Online Library All Journals
subjects Adult
Antibiotics. Antiinfectious agents. Antiparasitic agents
Antiviral agents
Antiviral Agents - administration & dosage
Biological and medical sciences
Drug Administration Schedule
Female
Genotype
Hepatitis C, Chronic - drug therapy
Hepatitis C, Chronic - genetics
Human viral diseases
Humans
Infectious diseases
Interferon-alpha - administration & dosage
Male
Medical sciences
Middle Aged
Pharmacology. Drug treatments
Polyethylene Glycols
Recombinant Proteins
Ribavirin - administration & dosage
RNA, Viral
Viral diseases
Viral hepatitis
Viral Load
title Pegylated interferon alpha‐2b plus ribavirin in patients with genotype 4 chronic hepatitis C: The role of rapid and early virologic response
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-08T13%3A48%3A45IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Pegylated%20interferon%20alpha%E2%80%902b%20plus%20ribavirin%20in%20patients%20with%20genotype%204%20chronic%20hepatitis%20C:%20The%20role%20of%20rapid%20and%20early%20virologic%20response&rft.jtitle=Hepatology%20(Baltimore,%20Md.)&rft.au=Kamal,%20Sanaa%20M.&rft.date=2007-12&rft.volume=46&rft.issue=6&rft.spage=1732&rft.epage=1740&rft.pages=1732-1740&rft.issn=0270-9139&rft.eissn=1527-3350&rft.coden=HPTLD9&rft_id=info:doi/10.1002/hep.21917&rft_dat=%3Cproquest_cross%3E69025981%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=69025981&rft_id=info:pmid/17943989&rfr_iscdi=true