Virological suppression at 6 months is related to choice of initial regimen in anti retroviral-naive patients: a cohort study

被引:89
作者
Matthews, GV
Sabin, CA
Mandalia, S
Lampe, F
Phillips, AN
Nelson, MR
Bower, M
Johnson, MA
Gazzard, BG
机构
[1] Chelsea & Westminster Hosp, Dept HIV Med, London SW10 9NH, England
[2] Royal Free Ctr HIV Med, London, England
[3] Dept Primary Care & Populat Sci, London, England
关键词
antiretroviral therapy; observational cohorts; HIV-1 viral load;
D O I
10.1097/00002030-200201040-00008
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background: Guidelines recommend both protease inhibitor (PI)- and non-nucleoside reverse transcriptase inhibitor (NNRTI)-containing regimens for initial therapy in HIV-positive individuals whilst clinical trial data comparing treatment options remain limited. Objective: To assess whether drug selection (PI versus NNRTI) in anti retroviral-naive patients is related to virological response at 6 months within a clinical cohort. Design: Databases from two large clinics were used to identify all treatment-naive patients initiating highly active antiretroviral therapy (PI/ two PI or NNRTI). Statistical models determined the likelihood of suppressing HIV viral load < 500 copies/ml, the risk of treatment failure by 6 months, and factors associated with treatment success. Results: Of 1109 potentially eligible patients 888 met study criteria and were included; 484 were prescribed a PI (40% indinavir, 41% nelfinavir) and 404 were prescribed NNRTI (40% efavirenz, 60% nevirapine). Three treatment arms were compared: efavirenz versus nevirapine versus PI. After stratification by year and centre and adjustment for baseline variables, only treatment group and baseline viral load remained significantly associated with virological suppression at 6 months. Patients on efavirenz were significantly more likely to achieve an undetectable viral load than those on PI or nevirapine. The relative hazard for nevirapine was 0.77 (95% confidence interval, 0.61-0.96, P = 0.02) and that for PI was 0.74 (95% confidence interval, 0.58-0.94, P=0.01), Efavirenz also performed better in the analysis of treatment failure at 6 months. Conclusion: Although observational cohort data may be susceptible to significant bias, this study suggests a better initial virological response for efavirenz compared to either nevirapine or the PI. Clinical trial data is required to confirm these findings. (C) 2002 Lippincott Williams Wilkins.
引用
收藏
页码:53 / 61
页数:9
相关论文
共 28 条
[1]   Antiretroviral therapy in adults - Updated recommendations of the International AIDS Society-USA Panel [J].
Carpenter, CCJ ;
Cooper, DA ;
Fischl, MA ;
Gatell, JM ;
Gazzard, BG ;
Hammer, SM ;
Hirsch, MS ;
Jacobsen, DM ;
Katzenstein, DA ;
Montaner, JSG ;
Richman, DD ;
Saag, MS ;
Schechter, M ;
Schooley, RT ;
Vella, S ;
Yeni, PG ;
Volberding, PA .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2000, 283 (03) :381-390
[2]   HIV RNA and CD4 cell count response to protease inhibitor therapy in an urban AIDS clinic: Response to both initial and salvage therapy [J].
Deeks, SG ;
Hecht, FM ;
Swanson, M ;
Elbeik, T ;
Loftus, R ;
Cohen, PT ;
Grant, RM .
AIDS, 1999, 13 (06) :F35-F43
[3]  
Fischl MA, 1999, AIDS, V13, pS49
[4]  
Gartland M, 2000, AIDS, V14, P367, DOI 10.1097/00002030-200003100-00009
[5]   1998 revision to the British HIV Association guidelines for antiretroviral treatment of HIV seropositive individuals [J].
Gazzard, B ;
Moyle, G .
LANCET, 1998, 352 (9124) :314-316
[6]   Comparison of the effectiveness of non-nucleoside reverse transcriptase inhibitor-containing and protease inhibitor-containing regimens using observational databases [J].
Ghani, AC ;
Henley, WE ;
Donnelly, CA ;
Mayer, S ;
Anderson, RM .
AIDS, 2001, 15 (09) :1133-1142
[7]   Factors associated with clinical and virological failure in patients receiving a triple therapy including a protease inhibitor [J].
Grabar, S ;
Pradier, C ;
Le Corfec, E ;
Lancar, R ;
Allavena, C ;
Bentata, M ;
Berlureau, P ;
Dupont, C ;
Fabbro-Peray, P ;
Poizot-Martin, I ;
Costagliola, D .
AIDS, 2000, 14 (02) :141-149
[8]   Treatment with indinavir, zidovudine, and lamivudine in adults with human immunodeficiency virus infection and prior antiretroviral therapy [J].
Gulick, RM ;
Mellors, JW ;
Havlir, D ;
Eron, JJ ;
Gonzalez, C ;
McMahon, D ;
Richman, DD ;
Valentine, FT ;
Jonas, L ;
Meibohm, A ;
Emini, EA ;
Chodakewitz, JA .
NEW ENGLAND JOURNAL OF MEDICINE, 1997, 337 (11) :734-739
[9]   A controlled trial of two nucleoside analogues plus indinavir in persons with human immunodeficiency virus infection and CD4 cell counts of 200 per cubic millimeter or less [J].
Hammer, SM ;
Squires, KE ;
Hughes, MD ;
Grimes, JM ;
Demeter, LM ;
Currier, JS ;
Eron, JJ ;
Feinberg, JE ;
Balfour, HH ;
Dayton, LR ;
Chodakewitz, JA ;
Fischl, MA .
NEW ENGLAND JOURNAL OF MEDICINE, 1997, 337 (11) :725-733
[10]  
LEDERGERBER B, 1996, DRUGS, V52, P93