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The comparative effectiveness of NRTI-sparing dual regimens in emulated trials using observational data from the Swiss HIV Cohort Study.
Young, Jim; Scherrer, Alexandra U; Calmy, Alexandra; Tarr, Philip E; Bernasconi, Enos; Cavassini, Matthias; Hachfeld, Anna; Vernazza, Pietro; Günthard, Huldrych F; Bucher, Heiner C.
Afiliação
  • Young J; Basel Institute for Clinical Epidemiology and Biostatistics, University Hospital Basel, University of Basel, Basel, Switzerland.
  • Scherrer AU; Division of Infectious Diseases and Hospital Epidemiology, University Hospital and University of Zurich, Zurich, Switzerland.
  • Calmy A; Institute of Medical Virology, University of Zurich, Zurich, Switzerland.
  • Tarr PE; Division of Infectious Diseases, University Hospital Geneva, Geneva, Switzerland.
  • Bernasconi E; Infectious Diseases Service, University Department of Medicine, Cantonal Hospital Baselland, University of Basel, Bruderholz, Switzerland.
  • Cavassini M; Division of Infectious Diseases, Regional Hospital of Lugano, Lugano, Switzerland.
  • Hachfeld A; Division of Infectious Diseases, University Hospital Lausanne and University of Lausanne, Lausanne, Switzerland.
  • Vernazza P; Department of Infectious Diseases, Bern University Hospital and University of Bern, Bern, Switzerland.
  • Günthard HF; Division of Infectious Diseases and Hospital Epidemiology, Cantonal Hospital St Gallen, St Gallen, Switzerland.
  • Bucher HC; Division of Infectious Diseases and Hospital Epidemiology, University Hospital and University of Zurich, Zurich, Switzerland.
Antivir Ther ; 24(5): 343-353, 2019.
Article em En | MEDLINE | ID: mdl-30985290
ABSTRACT

BACKGROUND:

Nucleoside (or nucleotide) reverse transcriptase inhibitors (NRTIs) cause side effects in some patients, prompting the use of either partly or fully NRTI-sparing regimens.

METHODS:

We used data from the Swiss HIV Cohort Study to estimate the effectiveness of two new dolutegravir dual regimens relative to the alternative NRTI-sparing dual regimens that our clinicians used previously. We emulated two trials by propensity score matching case patients on the dolutegravir regimen with control patients on an alternative regimen. We analysed the case control sets using a Bayesian Cox model and estimated effectiveness as the percentage still on their trial regimen without virological failure at 48 weeks.

RESULTS:

In a comparison of partly NRTI-sparing regimens, 58 cases treated with dolutegravir were matched to 17 controls treated with boosted darunavir (both with lamivudine or emtricitabine). The estimated difference in effectiveness was 15% (95% credible interval [CrI] 2-33) and 12% (95% CrI 0-26) in two sequential analyses 1 year apart. In a comparison of fully NRTI-sparing regimens, 54 cases treated with dolutegravir were matched to 32 controls treated with raltegravir (both with boosted darunavir). The estimated difference in effectiveness was 9% (95% CrI -1-21) and 5% (95% CrI -4-15) in the two sequential analyses.

CONCLUSIONS:

Estimates of relative effectiveness suggest that both dolutegravir regimens are not inferior to these alternative regimens. All four regimens seem suitable for patients needing an NRTI-sparing regimen there were few virological failures and few treatment changes due to toxicity.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Infecções por HIV / HIV-1 / Inibidores da Transcriptase Reversa Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Infecções por HIV / HIV-1 / Inibidores da Transcriptase Reversa Idioma: En Ano de publicação: 2019 Tipo de documento: Article