Evolution of drug resistance in HIV-infected patients remaining on a virologically failing combination antiretroviral therapy regimen

被引:77
作者
Cozzi-Lepri, Alessandro
Phillips, Andrew N.
Ruiz, Lidia
Clotet, Bonaventura
Loveday, Clive
Kjaer, Jesper
Mens, Helene
Clumeck, Nathan
Viksna, Ludmila
Antunes, Francisco
Machala, Ladislav
Lundgren, Jens D.
机构
[1] UCL, Royal Free & Univ Coll Med Sch, Dept Primary Care & Populat Sci, London NW3 2PF, England
[2] IrsiCaixa Fdn, Badalona, Spain
[3] Lluita SIDA Fdn, Badalona, Spain
[4] Hvidovre Univ Hosp, Copenhagen HIV Programme, Copenhagen, Denmark
[5] Hvidovre Univ Hosp, Dept Infect Dis, Copenhagen, Denmark
[6] CHU St Pierre, Dept Infect Dis, Brussels, Belgium
[7] Riga Stradins Univ, Riga, Latvia
[8] Hosp Santa Maria, Lisbon, Portugal
[9] AIDS Centra FN Bulovka, Prague, Czech Republic
关键词
virologically failing regimen; drug resistance mutations; future drug options;
D O I
10.1097/QAD.0b013e3280141fdf
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Objective: To estimate the extent of drug resistance accumulation in patients kept on a virologically failing regimen and its determinants in the clinical setting. Design: The study focused on 110 patients of EuroSIDA on an unchanged regimen who had two genotypic tests performed at two time points (t(0) and t(1)) when viral load was > 400 copies/ml. Methods: Accumulation of resistance between to and t, was measured using genotypic susceptibility scores (GSS) obtained by counting the total number of active drugs (according to the Rega system v6.4.1) among all licensed antiretrovirals as of I January 2006. Patients were grouped according to the number of active drugs in the failing regimen at t(0) (GSS_f-t(0)). Results: At to, patients had been on the failing combination antiretroviral therapy (cART) for a median of 11 months (range, 6-50 months). Even patients with extensive resistance to the failing regimen were still receiving benefit from treatment. An overall 6-monthly increase of 1.96 (SD, 2.23) International Aids Society-mutations and an average loss of 1.25 (SD, 1.81) active drugs were estimated. in comparison with patients with GSS_f-t(0) = 0, the number of active drugs lost was -1.08 [95% confidence interval (CI), -2.13 to -0.03; P= 0.04] in those with GSS_f-t(0)of 0.5-1.5 and -1.24 (95% CI, -2.44 to -0.04; P = 0.04) in those with GSS_f-t(0) >= 2. Conclusions: In patients kept on the same virologically failing cART regimen for a median of 6 months, there was considerable accumulation of drug resistance mutations, particularly in patients with initial low level of resistance to the failing regimen. Randomized comparisons of maintenance treatment strategies while awaiting a new suppressive therapy to become available are warranted.(c) 2007 Lippincott Williams & Wilkins.
引用
收藏
页码:721 / 732
页数:12
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