New treatment strategies in non-responder patients with chronic hepatitis C
There is solid evidence that retreatment of non-responders with standard regimens of interferon monotherapy is of no clinical value. On the other hand, combination therapy with interferon and ribavirin now produces sustained response rates in non-responders similar to those of interferon monotherapy...
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Veröffentlicht in: | Journal of hepatology 1999, Vol.31 (1), p.184-188 |
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container_title | Journal of hepatology |
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creator | Schalm, Solko W. Brouwer, Johannes T. Bekkering, Frank C. van Rossum, Tekla G.J. |
description | There is solid evidence that retreatment of non-responders with standard regimens of interferon monotherapy is of no clinical value. On the other hand, combination therapy with interferon and ribavirin now produces sustained response rates in non-responders similar to those of interferon monotherapy in untreated patients. Consequently, retreatment of non-responders with the combination of interferon-ribavirin appears to be a valid treatment option.
The efficacy of retreatment with the interferon-ribavirin combination can probably be increased by modifying the first weeks of interferon therapy from standard (3 MU tiw) to induction (10 MU daily), and by extending the treatment period to 12 months.
In the next few years, the additive value of amantadine to interferon or to interferon-ribavirin combination in inducing sustained viral clearance should be explored.
For the many patients who still do not respond with viral clearance despite these new approaches, the goal of therapy might be shifted towards persistent ALT normalization in order to reduce the progression of liver disease. Drugs that can normalize serum ALT such as interferon, ursodeoxycholic acid, ribavirin and glycyrrhizin should be evaluated for this objective. |
doi_str_mv | 10.1016/S0168-8278(99)80398-5 |
format | Article |
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The efficacy of retreatment with the interferon-ribavirin combination can probably be increased by modifying the first weeks of interferon therapy from standard (3 MU tiw) to induction (10 MU daily), and by extending the treatment period to 12 months.
In the next few years, the additive value of amantadine to interferon or to interferon-ribavirin combination in inducing sustained viral clearance should be explored.
For the many patients who still do not respond with viral clearance despite these new approaches, the goal of therapy might be shifted towards persistent ALT normalization in order to reduce the progression of liver disease. Drugs that can normalize serum ALT such as interferon, ursodeoxycholic acid, ribavirin and glycyrrhizin should be evaluated for this objective.</description><identifier>ISSN: 0168-8278</identifier><identifier>ISSN: 0169-5185</identifier><identifier>EISSN: 1600-0641</identifier><identifier>DOI: 10.1016/S0168-8278(99)80398-5</identifier><identifier>PMID: 10622584</identifier><language>eng</language><publisher>Oxford: Elsevier B.V</publisher><subject>Alanine Transaminase - blood ; Amantadine - therapeutic use ; Antiviral Agents - therapeutic use ; Biological and medical sciences ; Chronic hepatitis C ; Combination therapy ; Drug Therapy, Combination ; Hepatitis C virus ; Hepatitis C virus RNA ; Hepatitis C, Chronic - blood ; Hepatitis C, Chronic - drug therapy ; Hepatitis C, Chronic - pathology ; Hepatitis C, Chronic - virology ; Human viral diseases ; Humans ; Infectious diseases ; Interferon ; Interferons - therapeutic use ; Medical sciences ; Ribavirin ; Ribavirin - therapeutic use ; Therapy ; Treatment Failure ; Viral diseases ; Viral hepatitis</subject><ispartof>Journal of hepatology, 1999, Vol.31 (1), p.184-188</ispartof><rights>1999</rights><rights>2000 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c419t-54d2af395773c8314064861bc53c8237889db3d50c7b5af9a24bcc1438d4a69d3</citedby><cites>FETCH-LOGICAL-c419t-54d2af395773c8314064861bc53c8237889db3d50c7b5af9a24bcc1438d4a69d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0168827899803985$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>309,310,314,776,780,3536,4009,4035,4036,25119,27902,27903,27904,65309</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=1224810$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10622584$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Schalm, Solko W.</creatorcontrib><creatorcontrib>Brouwer, Johannes T.</creatorcontrib><creatorcontrib>Bekkering, Frank C.</creatorcontrib><creatorcontrib>van Rossum, Tekla G.J.</creatorcontrib><title>New treatment strategies in non-responder patients with chronic hepatitis C</title><title>Journal of hepatology</title><addtitle>J Hepatol</addtitle><description>There is solid evidence that retreatment of non-responders with standard regimens of interferon monotherapy is of no clinical value. On the other hand, combination therapy with interferon and ribavirin now produces sustained response rates in non-responders similar to those of interferon monotherapy in untreated patients. Consequently, retreatment of non-responders with the combination of interferon-ribavirin appears to be a valid treatment option.
The efficacy of retreatment with the interferon-ribavirin combination can probably be increased by modifying the first weeks of interferon therapy from standard (3 MU tiw) to induction (10 MU daily), and by extending the treatment period to 12 months.
In the next few years, the additive value of amantadine to interferon or to interferon-ribavirin combination in inducing sustained viral clearance should be explored.
For the many patients who still do not respond with viral clearance despite these new approaches, the goal of therapy might be shifted towards persistent ALT normalization in order to reduce the progression of liver disease. Drugs that can normalize serum ALT such as interferon, ursodeoxycholic acid, ribavirin and glycyrrhizin should be evaluated for this objective.</description><subject>Alanine Transaminase - blood</subject><subject>Amantadine - therapeutic use</subject><subject>Antiviral Agents - therapeutic use</subject><subject>Biological and medical sciences</subject><subject>Chronic hepatitis C</subject><subject>Combination therapy</subject><subject>Drug Therapy, Combination</subject><subject>Hepatitis C virus</subject><subject>Hepatitis C virus RNA</subject><subject>Hepatitis C, Chronic - blood</subject><subject>Hepatitis C, Chronic - drug therapy</subject><subject>Hepatitis C, Chronic - pathology</subject><subject>Hepatitis C, Chronic - virology</subject><subject>Human viral diseases</subject><subject>Humans</subject><subject>Infectious diseases</subject><subject>Interferon</subject><subject>Interferons - therapeutic use</subject><subject>Medical sciences</subject><subject>Ribavirin</subject><subject>Ribavirin - therapeutic use</subject><subject>Therapy</subject><subject>Treatment Failure</subject><subject>Viral diseases</subject><subject>Viral hepatitis</subject><issn>0168-8278</issn><issn>0169-5185</issn><issn>1600-0641</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkEtLAzEQgIMoWh8_QclBRA-rySbZTU4ixReKHtRzyCazNtLu1iS1-O9NbVFvXmaY4ZsHH0L7lJxSQquzpxxkIctaHit1IglTshBraEArQgpScbqOBj_IFtqO8Y0Qwojim2iLkqosheQDdPcAc5wCmDSBLuGYgknw6iFi3-Gu74oAcdp3DgKemuQzE_HcpxG2o9B33uIRLPrJRzzcRRutGUfYW-Ud9HJ1-Ty8Ke4fr2-HF_eF5VSlQnBXmpYpUdfMSkZ5_lZWtLEilyWrpVSuYU4QWzfCtMqUvLGWciYdN5VybAcdLfdOQ_8-g5j0xEcL47HpoJ9FXSkmZSVEBsUStKGPMUCrp8FPTPjUlOiFRf1tUS8UaaX0t0W9mDtYHZg1E3B_ppbaMnC4Aky0ZtwG01kff7my5JKSjJ0vMcg2PjwEHW1WaMH5ADZp1_t_PvkCtBeORQ</recordid><startdate>1999</startdate><enddate>1999</enddate><creator>Schalm, Solko W.</creator><creator>Brouwer, Johannes T.</creator><creator>Bekkering, Frank C.</creator><creator>van Rossum, Tekla G.J.</creator><general>Elsevier B.V</general><general>Elsevier</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>1999</creationdate><title>New treatment strategies in non-responder patients with chronic hepatitis C</title><author>Schalm, Solko W. ; Brouwer, Johannes T. ; Bekkering, Frank C. ; van Rossum, Tekla G.J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c419t-54d2af395773c8314064861bc53c8237889db3d50c7b5af9a24bcc1438d4a69d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>Alanine Transaminase - blood</topic><topic>Amantadine - therapeutic use</topic><topic>Antiviral Agents - therapeutic use</topic><topic>Biological and medical sciences</topic><topic>Chronic hepatitis C</topic><topic>Combination therapy</topic><topic>Drug Therapy, Combination</topic><topic>Hepatitis C virus</topic><topic>Hepatitis C virus RNA</topic><topic>Hepatitis C, Chronic - blood</topic><topic>Hepatitis C, Chronic - drug therapy</topic><topic>Hepatitis C, Chronic - pathology</topic><topic>Hepatitis C, Chronic - virology</topic><topic>Human viral diseases</topic><topic>Humans</topic><topic>Infectious diseases</topic><topic>Interferon</topic><topic>Interferons - therapeutic use</topic><topic>Medical sciences</topic><topic>Ribavirin</topic><topic>Ribavirin - therapeutic use</topic><topic>Therapy</topic><topic>Treatment Failure</topic><topic>Viral diseases</topic><topic>Viral hepatitis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Schalm, Solko W.</creatorcontrib><creatorcontrib>Brouwer, Johannes T.</creatorcontrib><creatorcontrib>Bekkering, Frank C.</creatorcontrib><creatorcontrib>van Rossum, Tekla G.J.</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>Journal of hepatology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Schalm, Solko W.</au><au>Brouwer, Johannes T.</au><au>Bekkering, Frank C.</au><au>van Rossum, Tekla G.J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>New treatment strategies in non-responder patients with chronic hepatitis C</atitle><jtitle>Journal of hepatology</jtitle><addtitle>J Hepatol</addtitle><date>1999</date><risdate>1999</risdate><volume>31</volume><issue>1</issue><spage>184</spage><epage>188</epage><pages>184-188</pages><issn>0168-8278</issn><issn>0169-5185</issn><eissn>1600-0641</eissn><abstract>There is solid evidence that retreatment of non-responders with standard regimens of interferon monotherapy is of no clinical value. On the other hand, combination therapy with interferon and ribavirin now produces sustained response rates in non-responders similar to those of interferon monotherapy in untreated patients. Consequently, retreatment of non-responders with the combination of interferon-ribavirin appears to be a valid treatment option.
The efficacy of retreatment with the interferon-ribavirin combination can probably be increased by modifying the first weeks of interferon therapy from standard (3 MU tiw) to induction (10 MU daily), and by extending the treatment period to 12 months.
In the next few years, the additive value of amantadine to interferon or to interferon-ribavirin combination in inducing sustained viral clearance should be explored.
For the many patients who still do not respond with viral clearance despite these new approaches, the goal of therapy might be shifted towards persistent ALT normalization in order to reduce the progression of liver disease. Drugs that can normalize serum ALT such as interferon, ursodeoxycholic acid, ribavirin and glycyrrhizin should be evaluated for this objective.</abstract><cop>Oxford</cop><pub>Elsevier B.V</pub><pmid>10622584</pmid><doi>10.1016/S0168-8278(99)80398-5</doi><tpages>5</tpages></addata></record> |
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subjects | Alanine Transaminase - blood Amantadine - therapeutic use Antiviral Agents - therapeutic use Biological and medical sciences Chronic hepatitis C Combination therapy Drug Therapy, Combination Hepatitis C virus Hepatitis C virus RNA Hepatitis C, Chronic - blood Hepatitis C, Chronic - drug therapy Hepatitis C, Chronic - pathology Hepatitis C, Chronic - virology Human viral diseases Humans Infectious diseases Interferon Interferons - therapeutic use Medical sciences Ribavirin Ribavirin - therapeutic use Therapy Treatment Failure Viral diseases Viral hepatitis |
title | New treatment strategies in non-responder patients with chronic hepatitis C |
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