Literature DB >> 23432466

The use of nucleoside reverse transcriptase inhibitors sparing regimens in treatment-experienced HIV-1 infected patients.

Antonio Di Biagio1, Elena Ricci, Claudio Viscoli, Alessio Mesini, Barbara Menzaghi, Laura Carenzi, Giancarlo Orofino, Giustino Parruti, Canio Martinelli, Giordano Madeddu, Giuseppe Vittorio De Socio, Marco Franzetti, Tiziana Quirino, Paolo Bonfanti.   

Abstract

Despite the relative lack of data, nucleoside/nucleotide reverse transcriptase inhibitor (NRTI)-sparing regimens are increasingly prescribed in clinical practice in treatment-experienced HIV-1 infected patients. We aimed to assess the frequency of NRTI-sparing regimens among these subjects, and to evaluate and compare their safety and tolerability. Patients were included if enrolled in the currently ongoing cohorts (raltegravir and darunavir) of the Surveillance Cohort Long-Term Toxicity Antiretrovirals (SCOLTA) Project. The duration of treatment with antiretroviral therapy was evaluated using the Kaplan-Meier curve and NRTI-sparing and NRTI-based regimens were compared using the log-rank test. From 2006 to 2011, 689 experienced patients were analyzed, of whom 210 (30.5%) were on NRTI-sparing regimens. Patients on NRTI-sparing regimens were older (p=0.004) and had higher median CD4+ cell counts (p=0.002) than patients on NRTI-based regimens. The most frequent combination regimens were raltegravir plus darunavir/ritonavir (n=65; 30.95%) among patients on NRTI-sparing regimen and tenofovir DF/emtricitabine plus darunavir/ritonavir in the NRTI-containing group (n=102; 21.3%). There was no difference between groups in terms of total withdrawal, treatment discontinuation was more likely due to therapeutic failure in NRTI-sparing regimen. NRTI-sparing regimens should be evaluated in a prospective randomized trial.

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Year:  2013        PMID: 23432466     DOI: 10.2174/1570162x113119990036

Source DB:  PubMed          Journal:  Curr HIV Res        ISSN: 1570-162X            Impact factor:   1.581


  4 in total

1.  Efficacy and tolerability of switching to a dual therapy with darunavir/ritonavir plus raltegravir in HIV-infected patients with HIV-1 RNA ≤50 cp/mL.

Authors:  Giordano Madeddu; Stefano Rusconi; Alessandro Cozzi-Lepri; Simona Di Giambenedetto; Stefano Bonora; Alessia Carbone; Andrea De Luca; Nicola Gianotti; Antonio Di Biagio; Andrea Antinori
Journal:  Infection       Date:  2017-05-05       Impact factor: 3.553

2.  HIV Salvage Therapy Does Not Require Nucleoside Reverse Transcriptase Inhibitors: A Randomized, Controlled Trial.

Authors:  Karen T Tashima; Laura M Smeaton; Carl J Fichtenbaum; Adriana Andrade; Joseph J Eron; Rajesh T Gandhi; Victoria A Johnson; Karin L Klingman; Justin Ritz; Sally Hodder; Jorge L Santana; Timothy Wilkin; Richard H Haubrich
Journal:  Ann Intern Med       Date:  2015-11-24       Impact factor: 25.391

3.  Maintenance of Viral Suppression after Optimization Therapy from Etravirine Plus Raltegravir to Rilpivirine Plus Dolutegravir in HIV-1-Infected Patients.

Authors:  Niccolò Riccardi; Filippo Del Puente; Lucia Taramasso; Antonio Di Biagio
Journal:  J Int Assoc Provid AIDS Care       Date:  2019 Jan-Dec

4.  Brief Report: Switch to Ritonavir-Boosted Atazanavir Plus Raltegravir in Virologically Suppressed Patients With HIV-1 Infection: A Randomized Pilot Study.

Authors:  Jan van Lunzen; Anton Pozniak; Jose M Gatell; Andrea Antinori; Isabelle Klauck; Oscar Serrano; Adyb Baakili; Olayemi Osiyemi; Heather Sevinsky; Pierre-Marie Girard
Journal:  J Acquir Immune Defic Syndr       Date:  2016-04-15       Impact factor: 3.731

  4 in total

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