Response to Efavirenz-Containing Regimens in Previously Antiretroviral-Naive HIV-Positive Patients: The Role of Gender

BACKGROUND:We investigated the role of gender on response to efavirenz (EFV)-containing regimens in previously antiretroviral-naive patients. METHODS:All previously antiretroviral-naive individuals from the Royal Free Hospital in London starting EFV from 1996 onward were included. Treatment failure...

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Veröffentlicht in:Journal of acquired immune deficiency syndromes (1999) 2007-09, Vol.46 (1), p.62-67
Hauptverfasser: Smith, Colette J, Sabin, Caroline A, Youle, Mike S, Lampe, Fiona C, Bhagani, Sanjay, Madge, Sara, Puradiredja, Dewi, Johnson, Margaret A, Phillips, Andrew N
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container_issue 1
container_start_page 62
container_title Journal of acquired immune deficiency syndromes (1999)
container_volume 46
creator Smith, Colette J
Sabin, Caroline A
Youle, Mike S
Lampe, Fiona C
Bhagani, Sanjay
Madge, Sara
Puradiredja, Dewi
Johnson, Margaret A
Phillips, Andrew N
description BACKGROUND:We investigated the role of gender on response to efavirenz (EFV)-containing regimens in previously antiretroviral-naive patients. METHODS:All previously antiretroviral-naive individuals from the Royal Free Hospital in London starting EFV from 1996 onward were included. Treatment failure was defined as the first of 2 consecutive viral load measurements >500 copies/mL more than 24 weeks after starting EFV. Standard survival methods were used to assess time to discontinuation and to treatment failure. RESULTS:Ninety-six women and 337 men were included. Women were mostly of black African ethnicity (64.6%) with a heterosexual risk (94.8%), whereas men were mostly white (66.8%; P < 0.0001) with a homosexual risk (71.2%; P < 0.0001). Women had lower CD4 counts when starting EFV (median [interquartile range [IQR] = 126 [36, 220] cells/mm for women vs. 190 [109, 268] cells/mm for men; P = 0.0003). After 48 and 96 weeks, 38.8% (95% confidence interval [CI]28.8% to 48.7%) and 56.3% (95% CI45.8% to 66.9%) of women had discontinued EFV compared with 28.3% (95% CI23.4% to 33.2%) and 41.8% (95% CI36.3% to 47.3%) of men (P = 0.005). The percentage experiencing failure by 48 and 96 weeks when ignoring treatment changes but censoring at the date of discontinuing all treatment was 1.3% (0.0%, 3.9%) and 4.4% (0.0%, 9.3%) for women compared with 3.8% (1.6%, 6.0%; P = 0.49) and 5.8% (3.0%, 8.6%) for men. Median (IQR) CD4 count increases at 48 weeks were +166 (+89, +239) cells/mm for women and +176 (+93, +263) cells/mm for men. CONCLUSIONS:Women seem to have comparable virologic and immunologic outcomes to first-line EFV-containing regimens compared with men, although they are more likely to discontinue the drug.
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METHODS:All previously antiretroviral-naive individuals from the Royal Free Hospital in London starting EFV from 1996 onward were included. Treatment failure was defined as the first of 2 consecutive viral load measurements &gt;500 copies/mL more than 24 weeks after starting EFV. Standard survival methods were used to assess time to discontinuation and to treatment failure. RESULTS:Ninety-six women and 337 men were included. Women were mostly of black African ethnicity (64.6%) with a heterosexual risk (94.8%), whereas men were mostly white (66.8%; P &lt; 0.0001) with a homosexual risk (71.2%; P &lt; 0.0001). Women had lower CD4 counts when starting EFV (median [interquartile range [IQR] = 126 [36, 220] cells/mm for women vs. 190 [109, 268] cells/mm for men; P = 0.0003). After 48 and 96 weeks, 38.8% (95% confidence interval [CI]28.8% to 48.7%) and 56.3% (95% CI45.8% to 66.9%) of women had discontinued EFV compared with 28.3% (95% CI23.4% to 33.2%) and 41.8% (95% CI36.3% to 47.3%) of men (P = 0.005). The percentage experiencing failure by 48 and 96 weeks when ignoring treatment changes but censoring at the date of discontinuing all treatment was 1.3% (0.0%, 3.9%) and 4.4% (0.0%, 9.3%) for women compared with 3.8% (1.6%, 6.0%; P = 0.49) and 5.8% (3.0%, 8.6%) for men. Median (IQR) CD4 count increases at 48 weeks were +166 (+89, +239) cells/mm for women and +176 (+93, +263) cells/mm for men. CONCLUSIONS:Women seem to have comparable virologic and immunologic outcomes to first-line EFV-containing regimens compared with men, although they are more likely to discontinue the drug.</description><identifier>ISSN: 1525-4135</identifier><identifier>EISSN: 1944-7884</identifier><identifier>DOI: 10.1097/QAI.0b013e31813e5e20</identifier><identifier>PMID: 17667341</identifier><identifier>CODEN: JDSRET</identifier><language>eng</language><publisher>Hagerstown, MD: Lippincott Williams &amp; Wilkins, Inc</publisher><subject>Adult ; AIDS/HIV ; Anti-HIV Agents - administration &amp; dosage ; Anti-HIV Agents - therapeutic use ; Antiretroviral drugs ; Benzoxazines - administration &amp; dosage ; Benzoxazines - therapeutic use ; Biological and medical sciences ; CD4 Lymphocyte Count ; Drug therapy ; Female ; Fundamental and applied biological sciences. Psychology ; HIV ; HIV Infections - drug therapy ; Human immunodeficiency virus ; Human viral diseases ; Humans ; Infectious diseases ; Male ; Medical sciences ; Microbiology ; Miscellaneous ; Risk factors ; Sex Characteristics ; Sexual behavior ; Time Factors ; Treatment Outcome ; Viral diseases ; Viral diseases of the lymphoid tissue and the blood. 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METHODS:All previously antiretroviral-naive individuals from the Royal Free Hospital in London starting EFV from 1996 onward were included. Treatment failure was defined as the first of 2 consecutive viral load measurements &gt;500 copies/mL more than 24 weeks after starting EFV. Standard survival methods were used to assess time to discontinuation and to treatment failure. RESULTS:Ninety-six women and 337 men were included. Women were mostly of black African ethnicity (64.6%) with a heterosexual risk (94.8%), whereas men were mostly white (66.8%; P &lt; 0.0001) with a homosexual risk (71.2%; P &lt; 0.0001). Women had lower CD4 counts when starting EFV (median [interquartile range [IQR] = 126 [36, 220] cells/mm for women vs. 190 [109, 268] cells/mm for men; P = 0.0003). After 48 and 96 weeks, 38.8% (95% confidence interval [CI]28.8% to 48.7%) and 56.3% (95% CI45.8% to 66.9%) of women had discontinued EFV compared with 28.3% (95% CI23.4% to 33.2%) and 41.8% (95% CI36.3% to 47.3%) of men (P = 0.005). The percentage experiencing failure by 48 and 96 weeks when ignoring treatment changes but censoring at the date of discontinuing all treatment was 1.3% (0.0%, 3.9%) and 4.4% (0.0%, 9.3%) for women compared with 3.8% (1.6%, 6.0%; P = 0.49) and 5.8% (3.0%, 8.6%) for men. Median (IQR) CD4 count increases at 48 weeks were +166 (+89, +239) cells/mm for women and +176 (+93, +263) cells/mm for men. 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Psychology</subject><subject>HIV</subject><subject>HIV Infections - drug therapy</subject><subject>Human immunodeficiency virus</subject><subject>Human viral diseases</subject><subject>Humans</subject><subject>Infectious diseases</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Microbiology</subject><subject>Miscellaneous</subject><subject>Risk factors</subject><subject>Sex Characteristics</subject><subject>Sexual behavior</subject><subject>Time Factors</subject><subject>Treatment Outcome</subject><subject>Viral diseases</subject><subject>Viral diseases of the lymphoid tissue and the blood. Aids</subject><subject>Viral Load</subject><subject>Virology</subject><subject>Women</subject><issn>1525-4135</issn><issn>1944-7884</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkk1vEzEQhlcIREvgHyBkIcHNZfyxH-YWRaWNVEGICteVd3e2cXHs1PamKr8eV40UqRd8GNvS885o5p2ieM_gjIGqv_ycL8-gAyZQsCbHEjm8KE6ZkpLWTSNf5nfJSyqZKE-KNzHeArBKSvW6OGF1VdVCstNiv8a48y4iSZ6cj3pvArq_dOFd0sYZd0PWeGO26CIxjqwC7o2fon0gc5cymoLPCm3pd232SC6Xv-nKR5MePyudDLoUv5LrDZK1t0j8SC7QDRjeFq9GbSO-O9yz4te38-vFJb36cbFczK9oL5pa0bJDDUoOdcOY7hX2QiNwNfC6Ruw6NmIpZc-kFhqQy1IBKN03rOJDJTUbxKz4_JR3F_zdhDG1WxN7tFY7zH20VSNF1sn_gpxBCZCHNis-PgNv_RRcbqLlQlS8UnWVIfkE9cHHGHBsd8FsdXhoGbSP7rXZvfa5e1n24ZB76rY4HEUHuzLw6QDo2Gs7Bu16E4-cApnHUx7r33ubMMQ_drrH0G5Q27Rp8x7wSghJOUANChhQyEeJf-_EszQ</recordid><startdate>20070901</startdate><enddate>20070901</enddate><creator>Smith, Colette J</creator><creator>Sabin, Caroline A</creator><creator>Youle, Mike S</creator><creator>Lampe, Fiona C</creator><creator>Bhagani, Sanjay</creator><creator>Madge, Sara</creator><creator>Puradiredja, Dewi</creator><creator>Johnson, Margaret A</creator><creator>Phillips, Andrew N</creator><general>Lippincott Williams &amp; Wilkins, Inc</general><general>Lippincott Williams &amp; Wilkins</general><general>Lippincott Williams &amp; Wilkins Ovid Technologies</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>7T2</scope><scope>7T5</scope><scope>7TK</scope><scope>7U7</scope><scope>7U9</scope><scope>C1K</scope><scope>H94</scope><scope>K9.</scope><scope>7U1</scope><scope>7U2</scope><scope>7X8</scope></search><sort><creationdate>20070901</creationdate><title>Response to Efavirenz-Containing Regimens in Previously Antiretroviral-Naive HIV-Positive Patients: The Role of Gender</title><author>Smith, Colette J ; Sabin, Caroline A ; Youle, Mike S ; Lampe, Fiona C ; Bhagani, Sanjay ; Madge, Sara ; Puradiredja, Dewi ; Johnson, Margaret A ; Phillips, Andrew N</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3879-5bea094d7811ac9ec3ae029d277eebb1fe544c14a3a0e2459009ac8162d64a1d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Adult</topic><topic>AIDS/HIV</topic><topic>Anti-HIV Agents - administration &amp; dosage</topic><topic>Anti-HIV Agents - therapeutic use</topic><topic>Antiretroviral drugs</topic><topic>Benzoxazines - administration &amp; dosage</topic><topic>Benzoxazines - therapeutic use</topic><topic>Biological and medical sciences</topic><topic>CD4 Lymphocyte Count</topic><topic>Drug therapy</topic><topic>Female</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>HIV</topic><topic>HIV Infections - drug therapy</topic><topic>Human immunodeficiency virus</topic><topic>Human viral diseases</topic><topic>Humans</topic><topic>Infectious diseases</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Microbiology</topic><topic>Miscellaneous</topic><topic>Risk factors</topic><topic>Sex Characteristics</topic><topic>Sexual behavior</topic><topic>Time Factors</topic><topic>Treatment Outcome</topic><topic>Viral diseases</topic><topic>Viral diseases of the lymphoid tissue and the blood. Aids</topic><topic>Viral Load</topic><topic>Virology</topic><topic>Women</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Smith, Colette J</creatorcontrib><creatorcontrib>Sabin, Caroline A</creatorcontrib><creatorcontrib>Youle, Mike S</creatorcontrib><creatorcontrib>Lampe, Fiona C</creatorcontrib><creatorcontrib>Bhagani, Sanjay</creatorcontrib><creatorcontrib>Madge, Sara</creatorcontrib><creatorcontrib>Puradiredja, Dewi</creatorcontrib><creatorcontrib>Johnson, Margaret A</creatorcontrib><creatorcontrib>Phillips, Andrew N</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>Health and Safety Science Abstracts (Full archive)</collection><collection>Immunology Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Risk Abstracts</collection><collection>Safety Science and Risk</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of acquired immune deficiency syndromes (1999)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Smith, Colette J</au><au>Sabin, Caroline A</au><au>Youle, Mike S</au><au>Lampe, Fiona C</au><au>Bhagani, Sanjay</au><au>Madge, Sara</au><au>Puradiredja, Dewi</au><au>Johnson, Margaret A</au><au>Phillips, Andrew N</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Response to Efavirenz-Containing Regimens in Previously Antiretroviral-Naive HIV-Positive Patients: The Role of Gender</atitle><jtitle>Journal of acquired immune deficiency syndromes (1999)</jtitle><addtitle>J Acquir Immune Defic Syndr</addtitle><date>2007-09-01</date><risdate>2007</risdate><volume>46</volume><issue>1</issue><spage>62</spage><epage>67</epage><pages>62-67</pages><issn>1525-4135</issn><eissn>1944-7884</eissn><coden>JDSRET</coden><abstract>BACKGROUND:We investigated the role of gender on response to efavirenz (EFV)-containing regimens in previously antiretroviral-naive patients. METHODS:All previously antiretroviral-naive individuals from the Royal Free Hospital in London starting EFV from 1996 onward were included. Treatment failure was defined as the first of 2 consecutive viral load measurements &gt;500 copies/mL more than 24 weeks after starting EFV. Standard survival methods were used to assess time to discontinuation and to treatment failure. RESULTS:Ninety-six women and 337 men were included. Women were mostly of black African ethnicity (64.6%) with a heterosexual risk (94.8%), whereas men were mostly white (66.8%; P &lt; 0.0001) with a homosexual risk (71.2%; P &lt; 0.0001). Women had lower CD4 counts when starting EFV (median [interquartile range [IQR] = 126 [36, 220] cells/mm for women vs. 190 [109, 268] cells/mm for men; P = 0.0003). After 48 and 96 weeks, 38.8% (95% confidence interval [CI]28.8% to 48.7%) and 56.3% (95% CI45.8% to 66.9%) of women had discontinued EFV compared with 28.3% (95% CI23.4% to 33.2%) and 41.8% (95% CI36.3% to 47.3%) of men (P = 0.005). The percentage experiencing failure by 48 and 96 weeks when ignoring treatment changes but censoring at the date of discontinuing all treatment was 1.3% (0.0%, 3.9%) and 4.4% (0.0%, 9.3%) for women compared with 3.8% (1.6%, 6.0%; P = 0.49) and 5.8% (3.0%, 8.6%) for men. Median (IQR) CD4 count increases at 48 weeks were +166 (+89, +239) cells/mm for women and +176 (+93, +263) cells/mm for men. CONCLUSIONS:Women seem to have comparable virologic and immunologic outcomes to first-line EFV-containing regimens compared with men, although they are more likely to discontinue the drug.</abstract><cop>Hagerstown, MD</cop><pub>Lippincott Williams &amp; Wilkins, Inc</pub><pmid>17667341</pmid><doi>10.1097/QAI.0b013e31813e5e20</doi><tpages>6</tpages></addata></record>
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subjects Adult
AIDS/HIV
Anti-HIV Agents - administration & dosage
Anti-HIV Agents - therapeutic use
Antiretroviral drugs
Benzoxazines - administration & dosage
Benzoxazines - therapeutic use
Biological and medical sciences
CD4 Lymphocyte Count
Drug therapy
Female
Fundamental and applied biological sciences. Psychology
HIV
HIV Infections - drug therapy
Human immunodeficiency virus
Human viral diseases
Humans
Infectious diseases
Male
Medical sciences
Microbiology
Miscellaneous
Risk factors
Sex Characteristics
Sexual behavior
Time Factors
Treatment Outcome
Viral diseases
Viral diseases of the lymphoid tissue and the blood. Aids
Viral Load
Virology
Women
title Response to Efavirenz-Containing Regimens in Previously Antiretroviral-Naive HIV-Positive Patients: The Role of Gender
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