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      <ref-type name="Journal Article">17</ref-type>
      <work-type>ACL : Articles dans des revues avec comité de lecture répertoriées par l'AERES</work-type>
      <contributors>
        <authors>
          <author>
            <style face="normal" font="default" size="100%">Landman, R.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Koulla-Shiro, S.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Sow, P. S.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Ngolle, M.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Diallo, M. B.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Gueye, N. F. N.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Le Moing, V.</style>
          </author>
          <author>
            <style face="bold" font="default" size="100%">Eymard-Duvernay, Sabrina</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Benalycherif, A.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Charpentier, C.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Peytavin, G.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Delaporte, Eric</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Girard, P. M.</style>
          </author>
        </authors>
      </contributors>
      <titles>
        <title>Evaluation of four Tenofovir-containing regimens as first-line treatments in Cameroon and Senegal : the ANRS 12115 DAYANA Trial</title>
        <secondary-title>Antiviral Therapy</secondary-title>
      </titles>
      <pages>51-59</pages>
      <keywords>
        <keyword>CAMEROUN</keyword>
        <keyword>SENEGAL</keyword>
      </keywords>
      <dates>
        <year>2014</year>
      </dates>
      <call-num>fdi:010062019</call-num>
      <language>ENG</language>
      <periodical>
        <full-title>Antiviral Therapy</full-title>
      </periodical>
      <isbn>1359-6535</isbn>
      <accession-num>ISI:000335231800005</accession-num>
      <number>1</number>
      <electronic-resource-num>10.3851/imp2675</electronic-resource-num>
      <urls>
        <related-urls>
          <url>https://www.documentation.ird.fr/hor/fdi:010062019</url>
        </related-urls>
        <pdf-urls>
          <url>https://www.documentation.ird.fr/intranet/publi/2014/06/010062019.pdf</url>
        </pdf-urls>
      </urls>
      <volume>19</volume>
      <remote-database-provider>Horizon (IRD)</remote-database-provider>
      <abstract>Background: The aim of the present study was to determine appropriate tenofovir-based regimens meriting evaluation in large-scale randomized trials among sub-Saharan African patients. Methods: This was a randomized open-label 96-week prospective pilot study evaluating four first-line regimens: tenofovir/emtricitabine/nevirapine (group 1),tenofovir/lopinavir/ritonavir(group 2), tenofovir/emtricitabine/zidovudine (group 3) and tenofovir/emtricitabine/ efavirenz (group 4) in antiretroviral-naive, HIV-1-infected patients in Senegal and Cameroon. The primary end point was defined as an HIV-1 RNA viral load &lt; 50 copies/ml (study detection limit) at week 16 in &gt;= 50% of patients using intention-to-treat analysis. Results: At baseline, 119 patients included were 34% male, had a median plasma viral load of 5.4 log 10 copies/ml and median CD4(+) T-cell count of 200 cells/mm(3) range 53-358). The primary end point was achieved for groups 1, 3 and 4 (58% [n=31], 62% [n=29] and 53% [n=30], respectively), but not for group 2 (38% [n=29]). At week 96, undetectable HIV-1 RNA had been achieved in 74% of patients in group 1, 38% in group 2, 72% in group 3 and 73% in group 4. Patients with detectable HIV-1 RNA at week 16 were more likely to have baseline HIV-1 RNA &gt;= 100,000 copies/ml (adjusted OR 5.56, 95% CI 1.72, 16.67). HIV mutations associated with protease inhibitor resistance emerged in three patients, all of whom were in group 2. Anaemia occurred in two group 3 patients and was the only serious treatment-related adverse event. Conclusions: Three efficient and safe tenofovir-based triple regimens were identified; the two-drug regimen (tenofovir/lopinavir/ritonavir) did not achieve the protocol-defined virological threshold of efficacy.</abstract>
      <custom6>052 ; 050 ; 020</custom6>
      <custom1>UR233</custom1>
      <custom7>Cameroun / Sénégal</custom7>
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