Reduced risk of Efavirenz Discontinuation in Naïve Patients Starting First‐Line Antiretroviral Therapy with Single Tablet versus dual Tablet Regimen

Author:

Fabbiani M12,Zaccarelli M3,Latini A4,Sterrantino G5,D'Ettorre G6,Grima P7,Mondi A2,Rossetti B8,Borchi B5,Giuliani M4,Antinori A3,De Luca A28,Di Giambenedetto S2

Affiliation:

1. Division of Infectious Diseases Department of Internal Medicine University of Milano‐Bicocca San Gerardo Hospital Monza Italy

2. Institute of Clinical Infectious Diseases Catholic University of Sacred Heart Rome Italy

3. Viral Immunodeficiency Unit National Institute for Infectious Diseases ‘Lazzaro Spallanzani’ Rome Italy

4. Unit of Infectious Dermatology San Gallicano Hospital Rome Italy

5. Infectious Diseases Unit Careggi University Hospital Florence Italy

6. Department of Infectious Diseases University ‘La Sapienza’ Rome Italy

7. Infectious Diseases Unit S. Caterina Novella Hospital Galatina (Lecce) Italy

8. Infectious Diseases Unit Siena University Hospital Siena Italy

Abstract

ObjectivesDespite not being approved in Europe as first‐line therapy, the efavirenz (EFV)‐containing single tablet regimen (STR) is frequently used in clinical practice in naïve patients but few data are available on this strategy. In our study, we aimed to assess the risk of EFV discontinuation in patients starting antiretroviral therapy with STR vs. nonSTR.MethodsThis was a multicentre study retrospectively enrolling naïve patients starting EFV+TDF+FTC. Patients were followed from the time of treatment initiation to the discontinuation of the EFV‐containing regimen, comparing STR vs. nonSTR. Two different analyses were performed: (A) nonSTR patients censored at the last observation (switch to STR not considered as the end of observation); (B) nonSTR patients censored at the time of switch to STR.ResultsThe study included 235 patients, of whom 74 (31.5%) directly started STR. Among patients starting nonSTR, 108 (67.1%) switched to STR after a median period of 6 months. Forty‐four EFV discontinuations were observed (13 among STR vs. 31 among nonSTR patients). The overall estimated probability of discontinuation was 30% at 5 years, about half (14.8%) of these occurring during the first year. Analysis A did not show significant differences between STR and nonSTR regarding the probability of efavirenz discontinuation (19.9% vs. 24.7% at 5 years, P = 0.630). In contrast, Analysis B showed that the probability of EFV discontinuation was similar (8.3%) between STR and nonSTR patients up to 8 months. Thereafter, a significantly higher rate of discontinuation was observed in nonSTR patients (47.5% vs. 19.9% at 5 years, P = 0.034).ConclusionsOur data suggest that an early switch to STR during the first months of treatment could reduce the risk of EFV discontinuation.

Publisher

Wiley

Reference17 articles.

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