Predictors of trend in CD4-positive T-cell count and mortality among HIV-1-infected individuals with virological failure to all three antiretroviral-drug classes

被引:248
作者
Ledergerber, B
Lundgren, JD
Walker, AS
Sabin, C
Justice, A
Reiss, P
Mussini, C
Wit, F
Monforte, AD
Weber, R
Fusco, G
Staszewski, S
Law, M
Hogg, R
Lampe, F
Gill, MJ
Castelli, F
Phillips, AN
Castelli, F
Fusco, GP
Gill, MJ
Hogg, R
Lampe, F
Law, M
Ledergerber, B
Lundgren, JD
Monforte, AD
Mussini, C
Phillips, AN
Reiss, P
Staszewski, S
Walker, AS
Rooney, P
Taylor, S
Couldwell, D
Austin, D
Block, M
Clemons, J
Finlayson, R
Law, M
Petoumenos, K
Quan, D
Smith, D
O'Connor, C
Gorton, C
Allen, D
Mulhall, B
Mutimer, K
Smith, D
Keeffe, N
机构
[1] Univ Zurich Hosp, Div Infect Dis & Hosp Epidemiol, CH-8091 Zurich, Switzerland
[2] Hvidovre Univ Hosp, Copenhagen HIV Programme, DK-2650 Hvidovre, Denmark
[3] MRC, Clin Trials Unit, London, England
[4] UCL Royal Free & Univ Coll Med Sch, London, England
[5] VA Pittsburgh Hlth Care Syst, Pittsburgh, PA USA
[6] Univ Amsterdam, Acad Med Ctr, NL-1105 AZ Amsterdam, Netherlands
[7] Natl AIDS Therapy Evaluat Ctr, Amsterdam, Netherlands
[8] Univ Modena, Clin Infect Dis, I-41100 Modena, Italy
[9] Int Antiviral Therapy Evaluat Ctr, Amsterdam, Netherlands
[10] Univ Milan, Inst Infect Dis, Milan, Italy
[11] GlaxoSmithKline Inc, Res Triangle Pk, NC USA
[12] Goethe Univ Frankfurt, D-6000 Frankfurt, Germany
[13] Univ New S Wales, Natl Ctr HIV Epidemiol & Clin Res, Darlinghurst, NSW, Australia
[14] Univ British Columbia, BC Ctr Excellence HIV AIDS, Vancouver, BC V5Z 1M9, Canada
[15] So Alberta Clin, Calgary, AB, Canada
[16] Univ Brescia, Inst Infect & Trop Dis, Brescia, Italy
基金
英国医学研究理事会;
关键词
D O I
10.1016/S0140-6736(04)16589-6
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Treatment strategies for patients in whom HIV replication is not suppressed after exposure to several drug classes remain unclear. We aimed to assess the inter-relations between viral load, CD4-cell count, and clinical outcome in patients who had experienced three-class virological failure. Methods We undertook collaborative joint analysis of 13 HIV cohorts from Europe, North America, and Australia, involving patients who had had three-class virological failure (viral load >1000 copies per mL for >4 months). Regression analyses were used to quantify the associations between CD4-cell-count slope, HIV-1 RNA concentration, treatment information, and demographic characteristics. Predictors of death were analysed by Cox's proportional-hazards models. Findings 2488 patients were included. 2118 (85%) had started antiretroviral therapy with single or dual therapy. During 5015 person-years of follow-up, 276 patients died (mortality rate 5.5 per 100 person-years; 3-year mortality risk 15.3% (95% Cl 13.5-17.3). Risk of death was strongly influenced by the latest CD4-cell count with a relative hazard of 15.8 (95% CI 9.28-27.0) for counts below 50 cells per muL versus above 200 cells per muL. The latest viral load did not independently predict death. For any given viral load, patients on treatment had more favourable CD4-cell-count slopes than those off treatment. For patients on treatment and with stable viral load, CD4-cell counts tended to be increasing at times when the current viral load was below 10 000 copies per mL or 1.5 log(10) copies per mL below off-treatment values. Interpretation In patients for whom viral-load suppression to below the level of detection is not possible, achievement and maintenance of a CD4-cell count above 200 per muL becomes the primary aim. Treatment regimens that maintain the viral load below 10 000 copies per mL or at least provide 1.5 log(10) copies per mL suppression below the off-treatment value do not seem to be associated with appreciable CD4-cell-count decline.
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页码:51 / 62
页数:12
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