Prognosis of HIV-1-infected patients starting highly active antiretroviral therapy:: a collaborative analysis of prospective studies

被引:1223
作者
Egger, M [1 ]
May, M
Chêne, G
Phillips, AN
Ledergerber, B
Dabis, F
Costagliola, D
Monforte, AD
de Wolf, F
Reiss, P
Lundgren, JD
Justice, AC
Staszewski, S
Leport, C
Hogg, RS
Sabin, CA
Gill, MJ
Salzberger, B
Sterne, JAC
机构
[1] Univ Bern, Dept Social & Prevent Med, CH-3012 Bern, Switzerland
[2] Univ Bristol, Dept Social Med, Bristol, Avon, England
[3] Univ Victor Seglen, INSERM, U330, Bordeaux, France
[4] UCL Royal Free & Univ Coll Med Sch, Dept Primary Care & Populat Sci, London, England
[5] Univ Zurich, Div Infect Dis & Hosp Epidemiol, Zurich, Switzerland
[6] Ctr Hosp Univ Pitie Salpetriere, INSERM, EMI 0214, Paris, France
[7] Univ Milan, Inst Infect & Trop Dis, Milan, Italy
[8] Univ Amsterdam, Acad Med Ctr, HIV Monitoring Fdn, NL-1105 AZ Amsterdam, Netherlands
[9] Univ Amsterdam, Acad Med Ctr, Natl AIDS Therpay Evaluat Ctr, NL-1105 AZ Amsterdam, Netherlands
[10] Univ London Imperial Coll Sci Technol & Med, Sch Med, Dept Infect Dis Epidemiol, London, England
[11] Hvidovre Univ Hosp, Dept Infect Dis, DK-2650 Hvidovre, Denmark
[12] VA Pittsburgh Healthcare Syst, Gen Internal Med Sect, Pittsburgh, PA USA
[13] Goethe Univ Frankfurt, Zentrum Inneren Med, Frankfurt, Germany
[14] Hop Bichat Claude Bernard, Serv Malad Infect & Trop, F-75877 Paris 18, France
[15] BC Ctr Excellence HIV AIDS, Div Epidemiol & Populat Hlth, Vancouver, BC, Canada
[16] Univ Calgary, Div Infect Dis, Calgary, AB, Canada
[17] Klinikum Univ Regensburg, Innere Med Klin 1, Regensburg, Germany
基金
英国医学研究理事会;
关键词
D O I
10.1016/S0140-6736(02)09411-4
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Insufficient data are available from single cohort studies to allow estimation of the prognosis of HIV-1 infected, treatment-naive patients who start highly active antiretroviral therapy (HAART). The ART Cohort Collaboration, which includes 13 cohort studies from Europe and North America, was established to fill this knowledge gap. Methods We analysed data on 12 574 adult patients starting HAART with a combination of at least three drugs. Data were analysed by intention-to-continue-treatment, ignoring treatment changes and interruptions. We considered progression to a combined endpoint of a new AIDS-defining disease or death, and to death alone. The prognostic model that generalised best was a Weibull model, stratified by baseline CD4 cell count and transmission group. Findings During 24 310 person-years of follow up, 1094 patients developed AIDS or died and 344 patients died. Baseline CD4 cell count was strongly associated with the probability of progression to AIDS or death: compared with patients starting HAART with less than 50 CD4 cells/muL, adjusted hazard ratios were 0.74 (95% CI 0.62-0.89) for 50-99 cells/muL, 0.52 (0.44-0.63) for 100-199 cells/muL, 0.24 (0.20-0.30) for 200-349 cells/muL, and 0.18 (0.14-0.22) for 350 or more CD4 cells/muL. Baseline HIV-1 viral load was associated with a higher probability of progression only if 100000 copies/mL or above. Other independent predictors of poorer outcome were advanced age, infection through injection-drug use, and a previous diagnosis of AIDS. The probability of progression to AIDS or death at 3 years ranged from 3.4% (2.8-4.1) in patients in the lowest-risk stratum for each prognostic variable, to 50% (43-58) in patients in the highest-risk strata. Interpretation The CD4 cell count at initiation was the dominant prognostic factor in patients starting HAART. Our findings have important implications for clinical management and should be taken into account in future treatment guidelines.
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页码:119 / 129
页数:11
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