Data Entry: Please note that the research database will be replaced by UNIverse by the end of October 2023. Please enter your data into the system https://universe-intern.unibas.ch. Thanks

Login for users with Unibas email account...

Login for registered users without Unibas email account...

 
Assessing efficacy of different nucleos(t)ide backbones in NNRTI-containing regimens in the Swiss HIV Cohort Study
JournalArticle (Originalarbeit in einer wissenschaftlichen Zeitschrift)
 
ID 4393095
Author(s) Yang, Wan-Lin; Kouyos, Roger D.; Scherrer, Alexandra U.; Boni, Jürg; Shah, Cyril; Yerly, Sabine; Klimkait, Thomas; Aubert, Vincent; Hirzel, Cédric; Battegay, Manuel; Cavassini, Matthias; Bernasconi, Enos; Vernazza, Pietro; Held, Leonhard; Ledergerber, Bruno; Günthard, Huldrych F.; Swiss, H. I. V. Cohort Study; Swiss, H. I. V. Cohort Study Shcs
Author(s) at UniBasel Klimkait, Thomas
Year 2015
Title Assessing efficacy of different nucleos(t)ide backbones in NNRTI-containing regimens in the Swiss HIV Cohort Study
Journal Journal of Antimicrobial Chemotherapy
Volume 70
Number 12
Pages / Article-Number 3323-31
Keywords Adult; Antiretroviral Therapy, Highly Active/*methods; Drug Resistance, Viral; Female; HIV Infections/*drug therapy; Hiv-1; Humans; Male; Middle Aged; Nucleosides/*therapeutic use; Nucleotides/*therapeutic use; Reverse Transcriptase Inhibitors/*therapeutic use; Switzerland; Treatment Failure
Mesh terms Adult; Antiretroviral Therapy, Highly Active, methods; Drug Resistance, Viral; Female; HIV Infections, drug therapy; HIV-1; Humans; Male; Middle Aged; Nucleosides, therapeutic use; Nucleotides, therapeutic use; Reverse Transcriptase Inhibitors, therapeutic use; Switzerland; Treatment Failure
Abstract BACKGROUND: The most recommended NRTI combinations as first-line antiretroviral treatment for HIV-1 infection in resource-rich settings are tenofovir/emtricitabine, abacavir/lamivudine, tenofovir/lamivudine and zidovudine/lamivudine. Efficacy studies of these combinations also considering pill numbers, dosing frequencies and ethnicities are rare. METHODS: We included patients starting first-line combination ART (cART) with or switching from first-line cART without treatment failure to tenofovir/emtricitabine, abacavir/lamivudine, tenofovir/lamivudine and zidovudine/lamivudine plus efavirenz or nevirapine. Cox proportional hazards regression was used to investigate the effect of the different NRTI combinations on two primary outcomes: virological failure (VF) and emergence of NRTI resistance. Additionally, we performed a pill burden analysis and adjusted the model for pill number and dosing frequency. RESULTS: Failure events per treated patient for the four NRTI combinations were as follows: 19/1858 (tenofovir/emtricitabine), 9/387 (abacavir/lamivudine), 11/344 (tenofovir/lamivudine) and 45/1244 (zidovudine/lamivudine). Compared with tenofovir/emtricitabine, abacavir/lamivudine had an adjusted HR for having VF of 2.01 (95% CI 0.86-4.55), tenofovir/lamivudine 2.89 (1.22-6.88) and zidovudine/lamivudine 2.28 (1.01-5.14), whereas for the emergence of NRTI resistance abacavir/lamivudine had an HR of 1.17 (0.11-12.2), tenofovir/lamivudine 11.3 (2.34-55.3) and zidovudine/lamivudine 4.02 (0.78-20.7). Differences among regimens disappeared when models were additionally adjusted for pill burden. However, non-white patients compared with white patients and higher pill number per day were associated with increased risks of VF and emergence of NRTI resistance: HR of non-white ethnicity for VF was 2.85 (1.64-4.96) and for NRTI resistance 3.54 (1.20-10.4); HR of pill burden for VF was 1.41 (1.01-1.96) and for NRTI resistance 1.72 (0.97-3.02). CONCLUSIONS: Although VF and emergence of resistance was very low in the population studied, tenofovir/emtricitabine appears to be superior to abacavir/lamivudine, tenofovir/lamivudine and zidovudine/lamivudine. However, it is unclear whether these differences are due to the substances as such or to an association of tenofovir/emtricitabine regimens with lower pill burden.
ISSN/ISBN 0305-7453 ; 1460-2091
URL https://www.ncbi.nlm.nih.gov/pubmed/26362944
edoc-URL https://edoc.unibas.ch/62186/
Full Text on edoc No
Digital Object Identifier DOI 10.1093/jac/dkv257
PubMed ID http://www.ncbi.nlm.nih.gov/pubmed/26362944
Document type (ISI) Journal Article
 
   

MCSS v5.8 PRO. 0.345 sec, queries - 0.000 sec ©Universität Basel  |  Impressum   |    
26/04/2024