Brief report: two-year outcome of a multidrug regimen in patients who did not respond to a protease inhibitor regimen
In most studies, people who have not responded virologically to a protease inhibitor (PI)-containing regimen have tended to experience poor virologic responses to subsequent regimens. We describe the 2-year viral load, CD4 count, and clinical outcome of a multidrug regimen used in 60 people who had...
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Veröffentlicht in: | Journal of acquired immune deficiency syndromes (1999) 2002-01, Vol.29 (1), p.58-61 |
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container_title | Journal of acquired immune deficiency syndromes (1999) |
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creator | Youle, Mike Tyrer, Mervyn Fisher, Martin Lampe, Fiona Wilson, Deborah Ransom, Darren Story, Alister Mocroft, Amanda Loveday, Clive Johnson, Margaret A Phillips, Andrew N |
description | In most studies, people who have not responded virologically to a protease inhibitor (PI)-containing regimen have tended to experience poor virologic responses to subsequent regimens. We describe the 2-year viral load, CD4 count, and clinical outcome of a multidrug regimen used in 60 people who had not responded virologically to a PI-containing regimen. At baseline, median CD4 count was 126/mm(3) (nadir 30/mm(3) ) and median viral load was 320,000 copies/mL. A median of five antiretroviral drugs had previously been used, of which a median of two were PIs. Of these patients, 16% had previously used another nonnucleoside reverse transcriptase inhibitor besides efavirenz. The multidrug regimen (median 5 drugs) started most commonly included efavirenz (100%), at least one PI (92%, usually indinavir/ritonavir), didanosine (78%), and hydroxyurea (74%). At year 2, 5 patients had died and 5 had no measure available. Nine patients developed a new AIDS event and 10 patients were known to have stopped all antiretroviral therapy. Thirty-one patients (52% of the whole group, 72% of those remaining on therapy with viral load value available) had viral load |
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We describe the 2-year viral load, CD4 count, and clinical outcome of a multidrug regimen used in 60 people who had not responded virologically to a PI-containing regimen. At baseline, median CD4 count was 126/mm(3) (nadir 30/mm(3) ) and median viral load was 320,000 copies/mL. A median of five antiretroviral drugs had previously been used, of which a median of two were PIs. Of these patients, 16% had previously used another nonnucleoside reverse transcriptase inhibitor besides efavirenz. The multidrug regimen (median 5 drugs) started most commonly included efavirenz (100%), at least one PI (92%, usually indinavir/ritonavir), didanosine (78%), and hydroxyurea (74%). At year 2, 5 patients had died and 5 had no measure available. Nine patients developed a new AIDS event and 10 patients were known to have stopped all antiretroviral therapy. Thirty-one patients (52% of the whole group, 72% of those remaining on therapy with viral load value available) had viral load <50 copies/mL. Thus, a substantial proportion of patients who had failed to respond virologically to PI-containing regimens can achieve profound and sustained virologic suppression with a multidrug regimen.</description><identifier>ISSN: 1525-4135</identifier><identifier>PMID: 11782591</identifier><language>eng</language><publisher>United States</publisher><subject>Acquired Immunodeficiency Syndrome - drug therapy ; Acquired Immunodeficiency Syndrome - immunology ; Acquired Immunodeficiency Syndrome - virology ; Adult ; AIDS/HIV ; Anti-HIV Agents - therapeutic use ; CD4 Lymphocyte Count ; Drug Therapy, Combination ; Female ; HIV Infections - drug therapy ; HIV Infections - immunology ; HIV Infections - virology ; HIV Protease Inhibitors - therapeutic use ; Humans ; Male ; Treatment Failure ; Treatment Outcome ; Viral Load</subject><ispartof>Journal of acquired immune deficiency syndromes (1999), 2002-01, Vol.29 (1), p.58-61</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11782591$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Youle, Mike</creatorcontrib><creatorcontrib>Tyrer, Mervyn</creatorcontrib><creatorcontrib>Fisher, Martin</creatorcontrib><creatorcontrib>Lampe, Fiona</creatorcontrib><creatorcontrib>Wilson, Deborah</creatorcontrib><creatorcontrib>Ransom, Darren</creatorcontrib><creatorcontrib>Story, Alister</creatorcontrib><creatorcontrib>Mocroft, Amanda</creatorcontrib><creatorcontrib>Loveday, Clive</creatorcontrib><creatorcontrib>Johnson, Margaret A</creatorcontrib><creatorcontrib>Phillips, Andrew N</creatorcontrib><title>Brief report: two-year outcome of a multidrug regimen in patients who did not respond to a protease inhibitor regimen</title><title>Journal of acquired immune deficiency syndromes (1999)</title><addtitle>J Acquir Immune Defic Syndr</addtitle><description>In most studies, people who have not responded virologically to a protease inhibitor (PI)-containing regimen have tended to experience poor virologic responses to subsequent regimens. We describe the 2-year viral load, CD4 count, and clinical outcome of a multidrug regimen used in 60 people who had not responded virologically to a PI-containing regimen. At baseline, median CD4 count was 126/mm(3) (nadir 30/mm(3) ) and median viral load was 320,000 copies/mL. A median of five antiretroviral drugs had previously been used, of which a median of two were PIs. Of these patients, 16% had previously used another nonnucleoside reverse transcriptase inhibitor besides efavirenz. The multidrug regimen (median 5 drugs) started most commonly included efavirenz (100%), at least one PI (92%, usually indinavir/ritonavir), didanosine (78%), and hydroxyurea (74%). At year 2, 5 patients had died and 5 had no measure available. Nine patients developed a new AIDS event and 10 patients were known to have stopped all antiretroviral therapy. Thirty-one patients (52% of the whole group, 72% of those remaining on therapy with viral load value available) had viral load <50 copies/mL. Thus, a substantial proportion of patients who had failed to respond virologically to PI-containing regimens can achieve profound and sustained virologic suppression with a multidrug regimen.</description><subject>Acquired Immunodeficiency Syndrome - drug therapy</subject><subject>Acquired Immunodeficiency Syndrome - immunology</subject><subject>Acquired Immunodeficiency Syndrome - virology</subject><subject>Adult</subject><subject>AIDS/HIV</subject><subject>Anti-HIV Agents - therapeutic use</subject><subject>CD4 Lymphocyte Count</subject><subject>Drug Therapy, Combination</subject><subject>Female</subject><subject>HIV Infections - drug therapy</subject><subject>HIV Infections - immunology</subject><subject>HIV Infections - virology</subject><subject>HIV Protease Inhibitors - therapeutic use</subject><subject>Humans</subject><subject>Male</subject><subject>Treatment Failure</subject><subject>Treatment Outcome</subject><subject>Viral Load</subject><issn>1525-4135</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo1kD1PwzAYhD2AaCn8BeSJLZI_G5sNKqBIlVi6R078pjVK4uAPVf33WKKdbrjnTqe7QUsqmawE5XKB7mP8IYSuhdB3aEFprZjUdInyW3DQ4wCzD-kFp5OvzmAC9jl1fgTse2zwmIfkbMiHwh3cCBN2E55NcjCliE9Hj62zePKp-HH2k8XJl9gcfAITodBH17rkwzX_gG57M0R4vOgK7T_e95tttfv-_Nq87qpZCloZw9YWTG-BA1OUas4U14K0ikhGOAUumVozKUkNnGpV644SxnplDNBW9HyFnv9ry5LfDDE1o4sdDIOZwOfY1OUaVmtRwKcLmNsRbDMHN5pwbq4_8T_IUmPL</recordid><startdate>20020101</startdate><enddate>20020101</enddate><creator>Youle, Mike</creator><creator>Tyrer, Mervyn</creator><creator>Fisher, Martin</creator><creator>Lampe, Fiona</creator><creator>Wilson, Deborah</creator><creator>Ransom, Darren</creator><creator>Story, Alister</creator><creator>Mocroft, Amanda</creator><creator>Loveday, Clive</creator><creator>Johnson, Margaret A</creator><creator>Phillips, Andrew N</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>20020101</creationdate><title>Brief report: two-year outcome of a multidrug regimen in patients who did not respond to a protease inhibitor regimen</title><author>Youle, Mike ; 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We describe the 2-year viral load, CD4 count, and clinical outcome of a multidrug regimen used in 60 people who had not responded virologically to a PI-containing regimen. At baseline, median CD4 count was 126/mm(3) (nadir 30/mm(3) ) and median viral load was 320,000 copies/mL. A median of five antiretroviral drugs had previously been used, of which a median of two were PIs. Of these patients, 16% had previously used another nonnucleoside reverse transcriptase inhibitor besides efavirenz. The multidrug regimen (median 5 drugs) started most commonly included efavirenz (100%), at least one PI (92%, usually indinavir/ritonavir), didanosine (78%), and hydroxyurea (74%). At year 2, 5 patients had died and 5 had no measure available. Nine patients developed a new AIDS event and 10 patients were known to have stopped all antiretroviral therapy. Thirty-one patients (52% of the whole group, 72% of those remaining on therapy with viral load value available) had viral load <50 copies/mL. Thus, a substantial proportion of patients who had failed to respond virologically to PI-containing regimens can achieve profound and sustained virologic suppression with a multidrug regimen.</abstract><cop>United States</cop><pmid>11782591</pmid><tpages>4</tpages></addata></record> |
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subjects | Acquired Immunodeficiency Syndrome - drug therapy Acquired Immunodeficiency Syndrome - immunology Acquired Immunodeficiency Syndrome - virology Adult AIDS/HIV Anti-HIV Agents - therapeutic use CD4 Lymphocyte Count Drug Therapy, Combination Female HIV Infections - drug therapy HIV Infections - immunology HIV Infections - virology HIV Protease Inhibitors - therapeutic use Humans Male Treatment Failure Treatment Outcome Viral Load |
title | Brief report: two-year outcome of a multidrug regimen in patients who did not respond to a protease inhibitor regimen |
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