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Long-term immunologic and virologic responses on raltegravir-containing regimens among ART-experienced participants in the HIV Outpatient Study

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File Language:
English


Details

  • Alternative Title:
    HIV Clin Trials
  • Personal Author:
  • Corporate Authors:
  • Description:
    Objectives

    Raltegravir (RAL)-containing antiretroviral therapy (ART) produced better immunologic and virologic responses than optimized background ART in clinical trials of heavily ART-experienced patients, but few data exist on long-term outcomes in routine HIV care.

    Methods

    We studied ART-experienced HIV outpatient study (HOPS) participants seen at 10 US HIV-specialty clinics during 2007–2011. We identified patients who started (baseline date) either continuous ≥30 days of RAL-containing or RAL-sparing ART, and used propensity score (PS) matching methods to account for baseline clinical and demographic differences. We used Kaplan–Meier methods and log-rank tests for the matched subsets to evaluate probability of death, achieving HIV RNA <50 copies/ml, and CD4 cell count (CD4) increase of ≥50 cells mm−3 during follow-up.

    Results

    Among 784 RAL-exposed and 1062 RAL-unexposed patients, 472 from each group were matched by PS. At baseline, the 472 RAL-exposed patients (mean nadir CD4, 205 cells mm−3; mean baseline CD4, 460 cells mm−3; HIV RNA <50 copies ml−1 in 61%; mean years on prescribed ART, 7.5) were similar to RAL unexposed. During a mean follow-up of over 3 years, mortality rates and immunologic and virologic trajectories did not differ between the two groups. Among patients with detectable baseline HIV RNA levels, 76% of RAL-exposed and 63% of RAL-unexposed achieved HIV RNA <50 copies ml−1 (P=0.51); 69 and 58%, respectively, achieved a CD4 increase ≥50 cells mm−3 (P=0.70).

    Discussion

    In our large cohort of US ART-experienced patients with a wide spectrum of clinical history, similar outcomes were observed when prescribed RAL containing versus other contemporary ART.

  • Subjects:
  • Keywords:
  • Source:
    HIV Clin Trials. 16(4):139-146
  • Pubmed ID:
    26126549
  • Pubmed Central ID:
    PMC4657741
  • Document Type:
  • Funding:
  • Volume:
    16
  • Issue:
    4
  • Collection(s):
  • Main Document Checksum:
    urn:sha-512:43706e37e4c141464038acd55109235a0c16b1984580665b631b2aa6bc35c6ebd3d064dcf1c00eab23498cf51824f94ce27055e92665cea2f5e4a4b4c17eceb8
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    Filetype[PDF - 691.59 KB ]
File Language:
English
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