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Comparison between three quantitative assays in patients with chronic hepatitis C and their relevance in the prediction of response to therapy
To compare three quantitative assays measuring viral load in patients with chronic hepatitis C and to determine their value in predicting response to interferon (IFN) therapy, we analysed serum from 896 patients from eight European Centres using QUANTIPLEX™ bDNA, MONITOR AMPLICOR™ and SUPERQUANT™ as...
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Published in: | Journal of viral hepatitis 2000-05, Vol.7 (3), p.203-210 |
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creator | Pradat, P Chossegros, P Bailly, F Pontisso, P Saracco, G Sauleda, S Thursz, M Tillmann, H Vlassopoulou, H Alberti, A Braconier, J H Esteban, J I Hadziyannis, S Manns, M Rizzetto, M Thomas, H C Trépo, C |
description | To compare three quantitative assays measuring viral load in patients with chronic hepatitis C and to determine their value in predicting response to interferon (IFN) therapy, we analysed serum from 896 patients from eight European Centres using QUANTIPLEX™ bDNA, MONITOR AMPLICOR™ and SUPERQUANT™ assays. Analyses were performed on the same sample. Viral genotype was assessed using INNO‐LiPA HCV II kits. Intercentre variations were observed that were related to the handling of specimens not processed and stored within 6 h of blood sampling. Among sera with optimal handling, a stronger correlation was observed between bDNA and SUPERQUANT (0.806) than between bDNA and MONITOR (0.677) and between MONITOR and SUPERQUANT (0.632). These discrepancies were greatest with genotype 2 (bDNA/SUPERQUANT= 0.772; bDNA/MONITOR=0.456; SUPERQUANT/MONITOR= 0.299). This correlation was influenced by viraemia level and was better at lower viral loads. The proportion of sera with undetectable viral load was 15% with bDNA, 9.7% with MONITOR and 7.7% with SUPERQUANT. For the three measurements, the best cut‐offs of sustained response to IFN treatment were located at their detection threshold. Among patients with viral load below the detection level, a sustained response was observed in 35% tested with bDNA, 38% with MONITOR and 80% with SUPERQUANT. Hence a stronger correlation was observed between bDNA and SUPERQUANT than between either of these assays and MONITOR. SUPERQUANT was the most sensitive assay and this greater sensitivity was associated with a better predictive value of treatment response. |
doi_str_mv | 10.1046/j.1365-2893.2000.00224.x |
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Analyses were performed on the same sample. Viral genotype was assessed using INNO‐LiPA HCV II kits. Intercentre variations were observed that were related to the handling of specimens not processed and stored within 6 h of blood sampling. Among sera with optimal handling, a stronger correlation was observed between bDNA and SUPERQUANT (0.806) than between bDNA and MONITOR (0.677) and between MONITOR and SUPERQUANT (0.632). These discrepancies were greatest with genotype 2 (bDNA/SUPERQUANT= 0.772; bDNA/MONITOR=0.456; SUPERQUANT/MONITOR= 0.299). This correlation was influenced by viraemia level and was better at lower viral loads. The proportion of sera with undetectable viral load was 15% with bDNA, 9.7% with MONITOR and 7.7% with SUPERQUANT. For the three measurements, the best cut‐offs of sustained response to IFN treatment were located at their detection threshold. Among patients with viral load below the detection level, a sustained response was observed in 35% tested with bDNA, 38% with MONITOR and 80% with SUPERQUANT. Hence a stronger correlation was observed between bDNA and SUPERQUANT than between either of these assays and MONITOR. SUPERQUANT was the most sensitive assay and this greater sensitivity was associated with a better predictive value of treatment response.</description><identifier>ISSN: 1352-0504</identifier><identifier>EISSN: 1365-2893</identifier><identifier>DOI: 10.1046/j.1365-2893.2000.00224.x</identifier><identifier>PMID: 10849262</identifier><language>eng</language><publisher>Oxford UK: Blackwell Science Ltd</publisher><subject>AIDS/HIV ; Antiviral Agents - therapeutic use ; Cohort Studies ; Genotype ; Hepacivirus - genetics ; Hepacivirus - isolation & purification ; hepatitis C ; Hepatitis C virus ; Hepatitis C, Chronic - drug therapy ; Hepatitis C, Chronic - virology ; Humans ; Interferons - therapeutic use ; quantitative assay ; Reagent Kits, Diagnostic ; RNA, Viral - analysis ; Treatment Outcome ; treatment response ; Viral Load</subject><ispartof>Journal of viral hepatitis, 2000-05, Vol.7 (3), p.203-210</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4334-b8335627d74bd7a936cc52512ee61f5223e70fe94e21adf98e77bc45d5e6d5033</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10849262$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Pradat, P</creatorcontrib><creatorcontrib>Chossegros, P</creatorcontrib><creatorcontrib>Bailly, F</creatorcontrib><creatorcontrib>Pontisso, P</creatorcontrib><creatorcontrib>Saracco, G</creatorcontrib><creatorcontrib>Sauleda, S</creatorcontrib><creatorcontrib>Thursz, M</creatorcontrib><creatorcontrib>Tillmann, H</creatorcontrib><creatorcontrib>Vlassopoulou, H</creatorcontrib><creatorcontrib>Alberti, A</creatorcontrib><creatorcontrib>Braconier, J H</creatorcontrib><creatorcontrib>Esteban, J I</creatorcontrib><creatorcontrib>Hadziyannis, S</creatorcontrib><creatorcontrib>Manns, M</creatorcontrib><creatorcontrib>Rizzetto, M</creatorcontrib><creatorcontrib>Thomas, H C</creatorcontrib><creatorcontrib>Trépo, C</creatorcontrib><title>Comparison between three quantitative assays in patients with chronic hepatitis C and their relevance in the prediction of response to therapy</title><title>Journal of viral hepatitis</title><addtitle>J Viral Hepat</addtitle><description>To compare three quantitative assays measuring viral load in patients with chronic hepatitis C and to determine their value in predicting response to interferon (IFN) therapy, we analysed serum from 896 patients from eight European Centres using QUANTIPLEX™ bDNA, MONITOR AMPLICOR™ and SUPERQUANT™ assays. Analyses were performed on the same sample. Viral genotype was assessed using INNO‐LiPA HCV II kits. Intercentre variations were observed that were related to the handling of specimens not processed and stored within 6 h of blood sampling. Among sera with optimal handling, a stronger correlation was observed between bDNA and SUPERQUANT (0.806) than between bDNA and MONITOR (0.677) and between MONITOR and SUPERQUANT (0.632). These discrepancies were greatest with genotype 2 (bDNA/SUPERQUANT= 0.772; bDNA/MONITOR=0.456; SUPERQUANT/MONITOR= 0.299). This correlation was influenced by viraemia level and was better at lower viral loads. The proportion of sera with undetectable viral load was 15% with bDNA, 9.7% with MONITOR and 7.7% with SUPERQUANT. For the three measurements, the best cut‐offs of sustained response to IFN treatment were located at their detection threshold. Among patients with viral load below the detection level, a sustained response was observed in 35% tested with bDNA, 38% with MONITOR and 80% with SUPERQUANT. Hence a stronger correlation was observed between bDNA and SUPERQUANT than between either of these assays and MONITOR. SUPERQUANT was the most sensitive assay and this greater sensitivity was associated with a better predictive value of treatment response.</description><subject>AIDS/HIV</subject><subject>Antiviral Agents - therapeutic use</subject><subject>Cohort Studies</subject><subject>Genotype</subject><subject>Hepacivirus - genetics</subject><subject>Hepacivirus - isolation & purification</subject><subject>hepatitis C</subject><subject>Hepatitis C virus</subject><subject>Hepatitis C, Chronic - drug therapy</subject><subject>Hepatitis C, Chronic - virology</subject><subject>Humans</subject><subject>Interferons - therapeutic use</subject><subject>quantitative assay</subject><subject>Reagent Kits, Diagnostic</subject><subject>RNA, Viral - analysis</subject><subject>Treatment Outcome</subject><subject>treatment response</subject><subject>Viral Load</subject><issn>1352-0504</issn><issn>1365-2893</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2000</creationdate><recordtype>article</recordtype><recordid>eNqNkc1u1DAUhSMEon-8AvKKXVL_xonEBg20ZTSCDVCpG8txbjQeMk5qezozL8Ez4zRV1R2sfHXP-c6VdbIMEVwQzMvLTUFYKXJa1aygGOMCY0p5cXiVnT4Lr6dZ0BwLzE-ysxA2GBNGBXmbnRBc8ZqW9DT7sxi2o_Y2DA41EPcADsW1B0D3O-2ijTraB0A6BH0MyDo0pgW4GNDexjUyaz84a9Aapn20AS2Qdm2KAOuRhx4etDMwgWmFRg-tNdGmY0OX5DAOLgCKw6R6PR4vsjed7gO8e3rPs59XX34sbvLV9-uvi0-r3HDGeN5UjImSylbyppW6ZqUxIn2NApSkE5QykLiDmgMluu3qCqRsDBetgLIVmLHz7MOcO_rhfgchqq0NBvpeOxh2QUlCJMWC_tNIZIVrTKpkrGaj8UMIHjo1ervV_qgIVlNpaqOmbtTUjZpKU4-lqUNC3z_d2DVbaF-Ac0vJ8HE27G0Px_8OVstfN2lIeD7jNkQ4POPa_1alZFKo22_Xavn5anlb3a1S1l-O0rcu</recordid><startdate>200005</startdate><enddate>200005</enddate><creator>Pradat, P</creator><creator>Chossegros, P</creator><creator>Bailly, F</creator><creator>Pontisso, P</creator><creator>Saracco, G</creator><creator>Sauleda, S</creator><creator>Thursz, M</creator><creator>Tillmann, H</creator><creator>Vlassopoulou, H</creator><creator>Alberti, A</creator><creator>Braconier, J H</creator><creator>Esteban, J I</creator><creator>Hadziyannis, S</creator><creator>Manns, M</creator><creator>Rizzetto, M</creator><creator>Thomas, H C</creator><creator>Trépo, C</creator><general>Blackwell Science Ltd</general><scope>BSCLL</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>7U9</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>200005</creationdate><title>Comparison between three quantitative assays in patients with chronic hepatitis C and their relevance in the prediction of response to therapy</title><author>Pradat, P ; Chossegros, P ; Bailly, F ; Pontisso, P ; Saracco, G ; Sauleda, S ; Thursz, M ; Tillmann, H ; Vlassopoulou, H ; Alberti, A ; Braconier, J H ; Esteban, J I ; Hadziyannis, S ; Manns, M ; Rizzetto, M ; Thomas, H C ; Trépo, C</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4334-b8335627d74bd7a936cc52512ee61f5223e70fe94e21adf98e77bc45d5e6d5033</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2000</creationdate><topic>AIDS/HIV</topic><topic>Antiviral Agents - therapeutic use</topic><topic>Cohort Studies</topic><topic>Genotype</topic><topic>Hepacivirus - genetics</topic><topic>Hepacivirus - isolation & purification</topic><topic>hepatitis C</topic><topic>Hepatitis C virus</topic><topic>Hepatitis C, Chronic - drug therapy</topic><topic>Hepatitis C, Chronic - virology</topic><topic>Humans</topic><topic>Interferons - therapeutic use</topic><topic>quantitative assay</topic><topic>Reagent Kits, Diagnostic</topic><topic>RNA, Viral - analysis</topic><topic>Treatment Outcome</topic><topic>treatment response</topic><topic>Viral Load</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pradat, P</creatorcontrib><creatorcontrib>Chossegros, P</creatorcontrib><creatorcontrib>Bailly, F</creatorcontrib><creatorcontrib>Pontisso, P</creatorcontrib><creatorcontrib>Saracco, G</creatorcontrib><creatorcontrib>Sauleda, S</creatorcontrib><creatorcontrib>Thursz, M</creatorcontrib><creatorcontrib>Tillmann, H</creatorcontrib><creatorcontrib>Vlassopoulou, H</creatorcontrib><creatorcontrib>Alberti, A</creatorcontrib><creatorcontrib>Braconier, J H</creatorcontrib><creatorcontrib>Esteban, J I</creatorcontrib><creatorcontrib>Hadziyannis, S</creatorcontrib><creatorcontrib>Manns, M</creatorcontrib><creatorcontrib>Rizzetto, M</creatorcontrib><creatorcontrib>Thomas, H C</creatorcontrib><creatorcontrib>Trépo, C</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of viral hepatitis</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pradat, P</au><au>Chossegros, P</au><au>Bailly, F</au><au>Pontisso, P</au><au>Saracco, G</au><au>Sauleda, S</au><au>Thursz, M</au><au>Tillmann, H</au><au>Vlassopoulou, H</au><au>Alberti, A</au><au>Braconier, J H</au><au>Esteban, J I</au><au>Hadziyannis, S</au><au>Manns, M</au><au>Rizzetto, M</au><au>Thomas, H C</au><au>Trépo, C</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Comparison between three quantitative assays in patients with chronic hepatitis C and their relevance in the prediction of response to therapy</atitle><jtitle>Journal of viral hepatitis</jtitle><addtitle>J Viral Hepat</addtitle><date>2000-05</date><risdate>2000</risdate><volume>7</volume><issue>3</issue><spage>203</spage><epage>210</epage><pages>203-210</pages><issn>1352-0504</issn><eissn>1365-2893</eissn><abstract>To compare three quantitative assays measuring viral load in patients with chronic hepatitis C and to determine their value in predicting response to interferon (IFN) therapy, we analysed serum from 896 patients from eight European Centres using QUANTIPLEX™ bDNA, MONITOR AMPLICOR™ and SUPERQUANT™ assays. Analyses were performed on the same sample. Viral genotype was assessed using INNO‐LiPA HCV II kits. Intercentre variations were observed that were related to the handling of specimens not processed and stored within 6 h of blood sampling. Among sera with optimal handling, a stronger correlation was observed between bDNA and SUPERQUANT (0.806) than between bDNA and MONITOR (0.677) and between MONITOR and SUPERQUANT (0.632). These discrepancies were greatest with genotype 2 (bDNA/SUPERQUANT= 0.772; bDNA/MONITOR=0.456; SUPERQUANT/MONITOR= 0.299). This correlation was influenced by viraemia level and was better at lower viral loads. The proportion of sera with undetectable viral load was 15% with bDNA, 9.7% with MONITOR and 7.7% with SUPERQUANT. For the three measurements, the best cut‐offs of sustained response to IFN treatment were located at their detection threshold. Among patients with viral load below the detection level, a sustained response was observed in 35% tested with bDNA, 38% with MONITOR and 80% with SUPERQUANT. Hence a stronger correlation was observed between bDNA and SUPERQUANT than between either of these assays and MONITOR. SUPERQUANT was the most sensitive assay and this greater sensitivity was associated with a better predictive value of treatment response.</abstract><cop>Oxford UK</cop><pub>Blackwell Science Ltd</pub><pmid>10849262</pmid><doi>10.1046/j.1365-2893.2000.00224.x</doi><tpages>8</tpages></addata></record> |
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subjects | AIDS/HIV Antiviral Agents - therapeutic use Cohort Studies Genotype Hepacivirus - genetics Hepacivirus - isolation & purification hepatitis C Hepatitis C virus Hepatitis C, Chronic - drug therapy Hepatitis C, Chronic - virology Humans Interferons - therapeutic use quantitative assay Reagent Kits, Diagnostic RNA, Viral - analysis Treatment Outcome treatment response Viral Load |
title | Comparison between three quantitative assays in patients with chronic hepatitis C and their relevance in the prediction of response to therapy |
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