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Effectiveness of dolutegravir-based regimens as either first-line or switch antiretroviral therapy: data from the Icona cohort

Authors :
Mondi, A.
Cozzi-Lepri, A.
Tavelli, A.
Rusconi, S.
Vichi, F.
Ceccherini-Silberstein, F.
Calcagno, A.
De Luca, A.
Maggiolo, F.
Marchetti, G.
Antinori, A.
d'Arminio Monforte, A.
Andreoni, M.
Castagna, A.
Castelli, F.
Cauda, Roberto
Di Perri, G.
Galli, M.
Iardino, R.
Ippolito, Giuseppe
Azzarin, A.
Rezza, Giovanni
von Schloesser, F.
Viale, P.
Girardi, E.
Lo Caputo, S.
Mussini, C.
Puoti, M.
Perno, C. F.
Balotta, C.
Bandera, A.
Bonora, S.
Borderi, M.
Capetti, A.
Capobianchi, M. R.
Cicalini, S.
Cingolani, Antonella
Cinque, P.
Di Biagio, Anna
Gianotti, N.
Gori, A.
Guaraldi, G.
Lapadula, G.
Lichtner, M.
Madeddu, G.
Monno, L.
Nozza, S.
Quiros Roldan, E.
Rossotti, R.
Santoro, M. M.
Aracino, A.
Sarmati, L.
Fanti, I.
Lorenzini, P.
Rodano', A.
Macchia, M.
Carletti, F.
Carrara, S.
Di Caro, A.
Graziano, S.
Petrone, F.
Prota, G.
Quartu, S.
Truffa, S.
Giacometti, I. A.
Costantini, A.
Barocci, V.
Angarano, G.
Fabrizio, C.
Suardi, C.
I, V.
Verucchi, G.
Castelnuovo, F.
Minardi, C.
Menzaghi, B.
Abeli, C.
Cacopardo, Beatrice Marina
Celesia, B.
Vecchiet, J.
Falasca, K.
Pan, A.
Lorenzotti, S.
Sighinolfi, L.
Segala, D.
Blanc, P.
Cassola, G.
Viscoli, C.
Lessandrini, A.
Bobbio, N.
Mazzarello, G.
Pozzetto, I.
Bonfanti, P.
Molteni, C.
Chiodera, A.
Milini, P.
Nunnari, G.
Pellicano, G.
Rizzardini, G.
Bai, F.
Moioli, M. C.
Piolini, R.
Ridolfo, A. L.
Salpietro, S.
Tincati, C.
Puzzolante, C.
Migliorino, C.
Sangiovanni, V.
Borgia, G.
Esposito, V.
Di Martino, F.
Gentile, I.
Maddaloni, L.
Cattelan, A. M.
Marinello, S.
Cascio, A.
Colomba, C.
Baldelli, F.
Schiaroli, E.
Parruti, G.
Sozio, F.
Magnani, G.
Ursitti, M. A.
Cristaudo, A.
Vullo, V.
Acinapura, R.
Baldin, G.
Capozzi, M.
Rivano Capparucia, M.
Iaiani, G.
Atini, A.
Mastrorosa, I.
Plazzi, M. M.
Savinelli, S.
Vergori, A.
Cecchetto, M.
Viviani, F.
Bagella, P.
Rossetti, Barbara
Fontana Del Vecchio, R.
Francisci, D.
Di Giuli, C.
Caramello, P.
Orofino, G. C.
Sciandra, M.
Bassetti, M.
Ondero, A.
Pellizzer, G.
Manfrin, V.
Starnini, G.
Alungo, A.
Cauda R. (ORCID:0000-0002-1498-4229)
Ippolito G.
Rezza G.
Cingolani A. (ORCID:0000-0002-3793-2755)
Di Biagio A.
Cacopardo B.
Rossetti B.
Mondi, A.
Cozzi-Lepri, A.
Tavelli, A.
Rusconi, S.
Vichi, F.
Ceccherini-Silberstein, F.
Calcagno, A.
De Luca, A.
Maggiolo, F.
Marchetti, G.
Antinori, A.
d'Arminio Monforte, A.
Andreoni, M.
Castagna, A.
Castelli, F.
Cauda, Roberto
Di Perri, G.
Galli, M.
Iardino, R.
Ippolito, Giuseppe
Azzarin, A.
Rezza, Giovanni
von Schloesser, F.
Viale, P.
Girardi, E.
Lo Caputo, S.
Mussini, C.
Puoti, M.
Perno, C. F.
Balotta, C.
Bandera, A.
Bonora, S.
Borderi, M.
Capetti, A.
Capobianchi, M. R.
Cicalini, S.
Cingolani, Antonella
Cinque, P.
Di Biagio, Anna
Gianotti, N.
Gori, A.
Guaraldi, G.
Lapadula, G.
Lichtner, M.
Madeddu, G.
Monno, L.
Nozza, S.
Quiros Roldan, E.
Rossotti, R.
Santoro, M. M.
Aracino, A.
Sarmati, L.
Fanti, I.
Lorenzini, P.
Rodano', A.
Macchia, M.
Carletti, F.
Carrara, S.
Di Caro, A.
Graziano, S.
Petrone, F.
Prota, G.
Quartu, S.
Truffa, S.
Giacometti, I. A.
Costantini, A.
Barocci, V.
Angarano, G.
Fabrizio, C.
Suardi, C.
I, V.
Verucchi, G.
Castelnuovo, F.
Minardi, C.
Menzaghi, B.
Abeli, C.
Cacopardo, Beatrice Marina
Celesia, B.
Vecchiet, J.
Falasca, K.
Pan, A.
Lorenzotti, S.
Sighinolfi, L.
Segala, D.
Blanc, P.
Cassola, G.
Viscoli, C.
Lessandrini, A.
Bobbio, N.
Mazzarello, G.
Pozzetto, I.
Bonfanti, P.
Molteni, C.
Chiodera, A.
Milini, P.
Nunnari, G.
Pellicano, G.
Rizzardini, G.
Bai, F.
Moioli, M. C.
Piolini, R.
Ridolfo, A. L.
Salpietro, S.
Tincati, C.
Puzzolante, C.
Migliorino, C.
Sangiovanni, V.
Borgia, G.
Esposito, V.
Di Martino, F.
Gentile, I.
Maddaloni, L.
Cattelan, A. M.
Marinello, S.
Cascio, A.
Colomba, C.
Baldelli, F.
Schiaroli, E.
Parruti, G.
Sozio, F.
Magnani, G.
Ursitti, M. A.
Cristaudo, A.
Vullo, V.
Acinapura, R.
Baldin, G.
Capozzi, M.
Rivano Capparucia, M.
Iaiani, G.
Atini, A.
Mastrorosa, I.
Plazzi, M. M.
Savinelli, S.
Vergori, A.
Cecchetto, M.
Viviani, F.
Bagella, P.
Rossetti, Barbara
Fontana Del Vecchio, R.
Francisci, D.
Di Giuli, C.
Caramello, P.
Orofino, G. C.
Sciandra, M.
Bassetti, M.
Ondero, A.
Pellizzer, G.
Manfrin, V.
Starnini, G.
Alungo, A.
Cauda R. (ORCID:0000-0002-1498-4229)
Ippolito G.
Rezza G.
Cingolani A. (ORCID:0000-0002-3793-2755)
Di Biagio A.
Cacopardo B.
Rossetti B.
Publication Year :
2019

Abstract

Introduction: Concerns about dolutegravir (DTG) tolerability in the real-life setting have recently arisen. We aimed to estimate the risk of treatment discontinuation and virological failure of DTG-based regimens from a large cohort of HIV-infected individuals. Methods: We performed a multicentre, observational study including all antiretroviral therapy (ART)-naïve and virologically suppressed treatment-experienced (TE) patients from the Icona (Italian Cohort Naïve Antiretrovirals) cohort who started, for the first time, a DTG-based regimen from January 2015 to December 2017. We estimated the cumulative risk of DTG discontinuation regardless of the reason and for toxicity, and of virological failure using Kaplan–Meier curves. We used Cox regression model to investigate predictors of DTG discontinuation. Results: About 1679 individuals (932 ART-naïve, 747 TE) were included. The one- and two-year probabilities (95% CI) of DTG discontinuation were 6.7% (4.9 to 8.4) and 11.5% (8.7 to 14.3) for ART-naïve and 6.6% (4.6 to 8.6) and 7.6% (5.4 to 9.8) for TE subjects. In both ART-naïve and TE patients, discontinuations of DTG were mainly driven by toxicity with an estimated risk (95% CI) of 4.0% (2.6 to 5.4) and 2.5% (1.3 to 3.6) by one year and 5.6% (3.8 to 7.5) and 4.0% (2.4 to 5.6) by two years respectively. Neuropsychiatric events were the main reason for stopping DTG in both ART-naïve (2.1%) and TE (1.7%) patients. In ART-naïve, a concomitant AIDS diagnosis predicted the risk of discontinuing DTG for any reason (adjusted relative hazard (aRH) = 3.38, p = 0.001), whereas starting DTG in combination with abacavir (ABC) was associated with a higher risk of discontinuing because of toxicity (aRH = 3.30, p = 0.009). TE patients starting a DTG-based dual therapy compared to a triple therapy had a lower risk of discontinuation for any reason (adjusted hazard ratio (aHR) = 2.50, p = 0.037 for ABC-based triple-th

Details

Database :
OAIster
Notes :
English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1242040103
Document Type :
Electronic Resource