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Journal of the International AIDS Society logoLink to Journal of the International AIDS Society
. 2014 Nov 2;17(4Suppl 3):19814. doi: 10.7448/IAS.17.4.19814

ACTG-HIV symptoms changes in patients switched to RPV/FTC/TDF due to previous intolerance to CART. Interim analysis of the PRO-STR study

Daniel Podzamczer 1, Nerea Rozas 1, Pere Domingo 2, Antonio Ocampo 3, Eva Van den Eynde 1, Elisabeth Deig 4, Antonio Vergara 5, Hernando Knobel 6, Juan Pasquau 7, Antonio Antela 8, Manuel Crespo 9, Bonaventure Clotet 10, Jessica Muñoz 11, Pedro Fernandez 12, Paloma Geijo 13, Eduardo Rodríguez de Castro 14, Julio Diz 15, Araceli Casado 16, Covadonga Torres 16
PMCID: PMC4225323  PMID: 25397558

Abstract

Introduction

Tolerability and convenience are crucial aspects for the long-term success of combined antiretroviral therapy (cART). The aim of this study was to investigate the impact in routine clinical practice of switching to the single tablet regimen (STR) RPV/FTC/TDF in patients with intolerance to previous cART, in terms of patients’ well-being, assessed by several validated measures.

Methods

Prospective, multicenter study. Adult HIV-infected patients with viral load under 1.000 copies/mL while receiving a stable ART for at least the last three months and switched to RPV/FTC/TDF due to intolerance of previous regimen, were included. Analyses were performed by ITT. Presence/magnitude of symptoms (ACTG-HIV Symptom Index), quality of life (EQ-5D, EUROQoL & MOS-HIV), adherence (SMAQ), preference of treatment and perceived ease of medication (ESTAR) through 48 weeks were performed.

Results

Interim analysis of 125 patients with 16 weeks of follow up was performed. 100 (80%) were male, mean age 46 years. Mean CD4 at baseline was 629.5±307.29 and 123 (98.4%) had viral load <50 copies/mL; 15% were HCV co-infected. Ninety two (73.6%) patients switched from a NNRTI (84.8% from EFV/FTC/TDF) and 33 (26.4%) from a PI/r. The most frequent reasons for switching were psychiatric disorders (51.2%), CNS adverse events (40.8%), gastrointestinal (19.2%) and metabolic disorders (19.2%). At the time of this analysis (week 16), four patients (3.2%) discontinued treatment: one due to adverse events, two virologic failures and one with no data. A total of 104 patients (83.2%) were virologically suppressed (<50 copies/mL). The average degree of discomfort in the ACTG-HIV Symptom Index significantly decreased from baseline (21±15.55) to week 4 (10.89±12.36) & week 16 (10.81±12.62), p<0.001. In all the patients, quality of life tools showed a significant benefit in well-being of the patients (Table 1). Adherence to therapy significantly and progressively increased (SMAQ) from baseline (54.4%) to week 4 (68%), p<0.001 and to week 16 (72.0%), p<0.001.

Conclusions

Switching to RPV/FTC/TDF from another ARV regimen due to toxicity, significantly improved the quality of life of HIV-infected patients, both in mental and physical components, and improved adherence to therapy while maintaining a good immune and virological response.


Table 1.

Changes in quality of life tests alter switching to RPV/FTC/TDF

(n=125)

Quality of life tools Baseline Average (median)±sd Week 4 visit Average (median)±sd Δ p Week 16 visit Average (median)±sd Δ p
MOS-HIV
Physical component 81.28 (83.14) 9.80 84.84 (86.34) 10.23 3.56% 0.007 86.82 (87.16) 16.98 5.54% 0.003
Mental component 71.31 (75.10) 13.47 76.68 (78.37) 13.61 5.37% 0.001 77.27 (78.88) 10.14 5.96% <0.001
EQ-5D
EQ-5D Index Score/Value (population-based preference weights) 0.81 (0.80)±0.21 0.89 (1.0)±0.17 0.08 <0.001 0.92 (1.00)±0.14 0.11 <0.001
EUROQoL
Index Score 73.29 (75.00)±17.93 77.33 (80.00)±17.06 4.04 0.001 80.60 (80.00)±14.22 7.31 <0.001

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