4.4 Article

Comparing the efficacy of efavirenz and boosted lopinavir using viremia copy-years

Journal

Publisher

JOHN WILEY & SONS LTD
DOI: 10.7448/IAS.17.1.18617

Keywords

HIV-1 plasma viral load; antiretroviral therapy; clinical trial; area under the curve; cumulative viremia; efficacy; efavirenz; boosted lopinavir

Funding

  1. Ministry of Health Services, Province of British Columbia
  2. Knowledge Translation Award from the Canadian Institutes of Health Research and through an Avant-Garde Award from the National Institute on Drug Abuse, at the US National Institutes of Health [1DP1DA026182-01]
  3. National Council for Science and Technology (CONACYT, Mexico) [123-A1]
  4. CIHR/GSK Research Chair in Clinical Virology
  5. US National Institute on Drug Abuse [1 R03 DA033851-01]
  6. Scholar Award from the Michael Institute for Health Research
  7. Mexican Randomized Clinical Trial [NCT00162643]

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Introduction: HIV-1 plasma viral load during treatment can be highly variable. Thus, there is the need to find a measure of cumulative viremia that can be used to assess both the short-and long-term efficacy of highly active antiretroviral therapy (HAART). Here, we validate a measure of cumulative viremia to evaluate HAART efficacy. Methods: We accessed HAART efficacy using data from a randomized clinical trial conducted in Mexico. We compared the proportion of individuals achieving a viral load < 50 and < 400 copies/mL at week 48, against the cumulative plasma viral load, estimated as the area under the plasma viral load curve (AUVLC). High AUVLC indicates high cumulative viremia. Results and discussion: There was a strong and significant association between the proportion of individuals achieving a viral load < 50 and < 400 copies/mL at week 48, with individuals suppressed having significant lower cumulative viremia. The median area was 7513 (25th-75th percentile [Q1-Q3] 6634-8180) if viral load < 50 copies/mL and 7679 (Q1-Q3 6899-9373) if viral load >= 50 copies/mL (p-value 0.0284). When the analysis was stratified by study arm, individuals on efavirenz had lower cumulative viremia than those on boosted lopinavir. Conclusions: Our findings suggest that cumulative viremia should be explored further as a tool to simultaneously evaluate the individual and public health efficacy of HAART. This is particularly relevant to the implementation and evaluation of the Treatment 2.0 strategy recently proposed by UNAIDS and the WHO, as a means to maximize the individual and public health benefit of HAART.

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