Objective: The importance of an early reduction of HIV-1 RNA as a marker for positive longer term outcome is still under debate. We investigate whether antiretroviral-experienced patients receiving raltegravir plus etravirine have a higher early reduction of HIV-1 RNA compared with patients receiving raltegravir.
Design: An observational study of treatment-experienced patients.
Methods: The objective is to investigate 349 patients included in a raltegravir resistance study. The early outcome is defined as a reduction of HIV-1 RNA at week 8. The crude method defines all measurements below the limit of quantification to be equal to the limit of quantification provides biased estimates. Such a reduction is censored by the limit of quantification and is subject to selection bias in observational studies.
Results: The crude method showed a significant higher reduction in HIV-1 RNA reduction in patients receiving raltegravir plus etravirine compared with patients receiving raltegravir (mean reduction of 2.1 versus 1.8 log10 copies/mL). However, survival methods adjusted for both censoring, due to the limit of quantification, and confounding factors lead to a nonsignificant difference between the 2 treatment groups (mean reduction of 2.8 versus 2.7 log10 copies/mL).
Conclusion: Taking into account censoring and confounding factors, our study did not demonstrate a higher early reduction of HIV-1 RNA in patients receiving raltegravir with versus without etravirine.
*Sorbonne Universités, UPMC Université, INSERM UMR-S 1136, Institut Pierre Louis d'épidémiologie et de Santé Publique (IPLESP), Paris, France; and
†Laboratoire de Virologie AP-HP, Hôpital Pitié-Salpêtrière, INSERM UMR-S 1136, Institut Pierre Louis d'épidémiologie et de Santé Publique (IPLESP), Paris, France.
Correspondence to: Philippe Flandre, INSERM UMR-S 1136, 56 Boulevard Vincent Auriol, CS 81393, 75646 Paris Cedex 13, France (e-mail: philippe.flandre@iplesp.upmc.fr).
The authors have no funding or conflicts of interest to disclose.
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Received December 08, 2016
Accepted April 17, 2017