{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,1,15]],"date-time":"2026-01-15T01:55:05Z","timestamp":1768442105884,"version":"3.49.0"},"reference-count":38,"publisher":"Wiley","issue":"1","license":[{"start":{"date-parts":[[2016,6,28]],"date-time":"2016-06-28T00:00:00Z","timestamp":1467072000000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"funder":[{"DOI":"10.13039\/501100004963","name":"Seventh Framework Programme","doi-asserted-by":"publisher","id":[{"id":"10.13039\/501100004963","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["HIV Medicine"],"published-print":{"date-parts":[[2017,1]]},"abstract":"<jats:sec><jats:title>Objectives<\/jats:title><jats:p>We evaluated the virological response in patients starting a regimen based on darunavir\/ritonavir (<jats:styled-content style=\"fixed-case\">DRV<\/jats:styled-content>\/r), which is currently the most widely used ritonavir\u2010boosted protease inhibitor.<\/jats:p><\/jats:sec><jats:sec><jats:title>Methods<\/jats:title><jats:p>Data from 206 drug\u2010na\u00efve and 327 <jats:styled-content style=\"fixed-case\">PI<\/jats:styled-content>\u2010experienced patients starting <jats:styled-content style=\"fixed-case\">DRV<\/jats:styled-content>\/r 600\/100\u00a0mg twice daily (<jats:styled-content style=\"fixed-case\">DRV<\/jats:styled-content>600) or 800\/100\u00a0mg once daily (<jats:styled-content style=\"fixed-case\">DRV<\/jats:styled-content>800) were examined. The probabilities of virological success (<jats:styled-content style=\"fixed-case\">VS<\/jats:styled-content>) and virological rebound (<jats:styled-content style=\"fixed-case\">VR<\/jats:styled-content>) were evaluated in survival analyses. Baseline <jats:styled-content style=\"fixed-case\">DRV<\/jats:styled-content>\/r resistance and its evolution at failure were also examined.<\/jats:p><\/jats:sec><jats:sec><jats:title>Results<\/jats:title><jats:p><jats:styled-content style=\"fixed-case\">DRV<\/jats:styled-content>600 was preferentially administered in patients with complex requirements (older age, higher viraemia, lower <jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>4 cell count and <jats:styled-content style=\"fixed-case\">DRV<\/jats:styled-content>\/<jats:styled-content style=\"fixed-case\">PI<\/jats:styled-content> resistance) compared with <jats:styled-content style=\"fixed-case\">DRV<\/jats:styled-content>800. By 12\u00a0months, the probability of achieving <jats:styled-content style=\"fixed-case\">VS<\/jats:styled-content> was 93.2% and 84.3% in drug\u2010na\u00efve and <jats:styled-content style=\"fixed-case\">PI<\/jats:styled-content>\u2010experienced patients, respectively. The higher the baseline viraemia, the longer was the time required to achieve <jats:styled-content style=\"fixed-case\">VS<\/jats:styled-content>, both in drug\u2010na\u00efve patients [&gt;500\u00a0000 <jats:styled-content style=\"fixed-case\">HIV<\/jats:styled-content>\u20101 <jats:styled-content style=\"fixed-case\">RNA<\/jats:styled-content> copies\/<jats:styled-content style=\"fixed-case\">mL<\/jats:styled-content>: median [interquartile range (<jats:styled-content style=\"fixed-case\">IQR<\/jats:styled-content>)] 6.1 (5.1\u201310.3) months; 100\u00a0000\u2013500\u00a0000 copies\/<jats:styled-content style=\"fixed-case\">mL<\/jats:styled-content>: median (<jats:styled-content style=\"fixed-case\">IQR<\/jats:styled-content>) 4.9 (3.8\u20136.1) months; &lt;100\u00a0000 copies\/<jats:styled-content style=\"fixed-case\">mL<\/jats:styled-content>: median (<jats:styled-content style=\"fixed-case\">IQR<\/jats:styled-content>) 3.9 (3.5\u20134.8) months; <jats:italic>P<\/jats:italic>\u00a0&lt;\u00a00.001] and in <jats:styled-content style=\"fixed-case\">PI<\/jats:styled-content>\u2010experienced patients [\u2265100\u00a0000 copies\/<jats:styled-content style=\"fixed-case\">mL<\/jats:styled-content>: median (<jats:styled-content style=\"fixed-case\">IQR<\/jats:styled-content>) 7.2 (5.7\u201311.6) months; &lt;100\u00a0000 copies\/<jats:styled-content style=\"fixed-case\">mL<\/jats:styled-content>: median (<jats:styled-content style=\"fixed-case\">IQR<\/jats:styled-content>) 2.8 (2.4\u20133.3) months; <jats:italic>P<\/jats:italic>\u00a0&lt;\u00a00.001]. In <jats:styled-content style=\"fixed-case\">PI<\/jats:styled-content>\u2010experienced patients, the probability of <jats:styled-content style=\"fixed-case\">VR<\/jats:styled-content> was higher for higher viraemia levels (22.3% for \u2265100\u00a0000 copies\/ml <jats:italic>vs<\/jats:italic>. 9.7% for &lt;100\u00a0000 copies\/mL; <jats:italic>P<\/jats:italic>\u00a0=\u00a00.007). Baseline resistance did not affect the virological response. At failure, a high percentage of patients maintained virus susceptible to all <jats:styled-content style=\"fixed-case\">PI<\/jats:styled-content>s (drug\u2010na\u00efve: 95%; <jats:styled-content style=\"fixed-case\">PI<\/jats:styled-content>\u2010experienced: 80%). Despite being used more often in patients with more complex requirements, <jats:styled-content style=\"fixed-case\">DRV<\/jats:styled-content>600 performed as well as DRV800.<\/jats:p><\/jats:sec><jats:sec><jats:title>Conclusions<\/jats:title><jats:p>In clinical practice, use of <jats:styled-content style=\"fixed-case\">DRV<\/jats:styled-content>\/r (with its flexible dosage) results in high rates of virological response. These data support the use of <jats:styled-content style=\"fixed-case\">PI<\/jats:styled-content>\/r in patients whose characteristics require potent drugs with a high genetic barrier.<\/jats:p><\/jats:sec>","DOI":"10.1111\/hiv.12388","type":"journal-article","created":{"date-parts":[[2016,6,29]],"date-time":"2016-06-29T16:19:15Z","timestamp":1467217155000},"page":"21-32","source":"Crossref","is-referenced-by-count":10,"title":["Virological response and resistance profile in HIV\u20101\u2010infected patients starting darunavir\u2010containing regimens"],"prefix":"10.1111","volume":"18","author":[{"given":"D","family":"Armenia","sequence":"first","affiliation":[{"name":"Experimental Medicine and Surgery University of Rome Tor Vergata Rome Italy"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"D","family":"Di Carlo","sequence":"additional","affiliation":[{"name":"Experimental Medicine and Surgery University of Rome Tor Vergata Rome 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