Comparison of atazanavir/ritonavir and darunavir/ritonavir based antiretroviral therapy for antiretroviral naïve patients

نویسندگان

  • Tony Antoniou
  • Leah Szadkowski
  • Sharon Walmsley
  • Curtis Cooper
  • Ann N. Burchell
  • Ahmed M. Bayoumi
  • Julio S. G. Montaner
  • Mona Loutfy
  • Marina B. Klein
  • Nima Machouf
  • Christos Tsoukas
  • Alexander Wong
  • Robert S. Hogg
  • Janet Raboud
  • Robert Hogg
  • Simon Fraser
  • Ann N. Burchell
  • Curtis Cooper
  • Deborah Kelly
  • Marina Klein
  • Mona Loutfy
  • Nima Machouf
  • Julio Montaner
  • Janet Raboud
  • Chris Tsoukas
  • Stephen Sanche
  • Alexander Wong
  • Tony Antoniou
  • Ahmed Bayoumi
  • Mark Hull
  • Bohdan Nosyk
  • Angela Cescon
  • Michelle Cotterchio
  • Charlie Goldsmith
  • Silvia Guillemi
  • P. Richard Harrigan
  • Marianne Harris
  • Sean Hosein
  • Sharon JohnstonClaire Kendall
  • Clare Liddy
  • Viviane Lima
  • David Marsh
  • David Moore
  • Alexis Palmer
  • Sophie Patterson
  • Peter Phillips
  • Anita Rachlis
  • Sean B. Rourke
  • Hasina Samji
  • Marek Smieja
  • Benoit Trottier
  • Mark Wainberg
  • Sharon Walmsley
  • Chris Archibald
  • Ken Clement
  • Monique Doolittle-Romas
  • Laurie Edmiston
  • Sandra Gardner
  • Brian Huskins
  • Jerry Lawless
  • Douglas Lee
  • Renee Masching
  • Stephen Tattle
  • Alireza Zahirieh
  • Claire Allen
  • Stryker Calvez
  • Guillaume Colley
  • Jason Chia
  • Daniel Corsi
  • Louise Gilbert
  • Nada Gataric
  • Katelyn Merritt
  • Lucia Light
  • David Mackie
  • Costa Pexos
  • Susan Shurgold
  • Leah Szadkowski
  • Chrissi Galanakis
  • Benita Yipv
  • Jaime Younger
  • Julia Zhu
چکیده

BACKGROUND Atazanavir/ritonavir and darunavir/ritonavir are common protease inhibitor-based regimens for treating patients with HIV. Studies comparing these drugs in clinical practice are lacking. METHODS We conducted a retrospective cohort study of antiretroviral naïve participants in the Canadian Observational Cohort (CANOC) collaboration initiating atazanavir/ritonavir- or darunavir/ritonavir-based treatment. We used separate Fine and Gray competing risk regression models to compare times to regimen failure (composite of virologic failure or discontinuation for any reason). Additional endpoints included virologic failure, discontinuation due to virologic failure, discontinuation for other reasons, and virologic suppression. RESULTS We studied 222 patients treated with darunavir/ritonavir and 1791 patients treated with atazanavir/ritonavir. Following multivariable adjustment, there was no difference between darunavir/ritonavir and atazanavir-ritonavir in the risk of regimen failure (adjusted hazard ratio 0.76, 95% CI 0.56 to 1.03) Darunavir/ritonavir-treated patients were at lower risk of virologic failure relative to atazanavir/ritonavir treated patients (aHR 0.50, 95% CI 0.28 to 0.91), findings driven largely by high rates of virologic failure among atazanavir/ritonavir-treated patients in the province of British Columbia. Of 108 discontinuations due to virologic failure, all occurred in patients starting atazanavir/ritonavir. There was no difference between regimens in time to discontinuation for reasons other than virologic failure (aHR 0.93; 95% CI 0.65 to 1.33) or virologic suppression (aHR 0.99, 95% CI 0.82 to 1.21). CONCLUSIONS The risk of regimen failure was similar between patients treated with darunavir/ritonavir and atazanavir/ritonavir. Although darunavir/ritonavir was associated with a lower risk of virologic failure relative to atazanavir/ritonavir, this difference varied substantially by Canadian province and likely reflects regional variation in prescribing practices and patient characteristics.

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عنوان ژورنال:

دوره 17  شماره 

صفحات  -

تاریخ انتشار 2017