Survival in HIV-infected patients who have received zidovudine: Comparison of combination therapy with sequential monotherapy and continued zidovudine monotherapy

被引:27
作者
Graham, NMH
Hoover, DR
Park, LP
Stein, DS
Phair, JP
Mellors, JW
Detels, R
Saah, AJ
Taylor, E
Margolick, JB
Markham, R
McArthur, J
Farzadegan, H
Armenian, H
Chmiel, JS
Cohen, B
Wesch, J
Wolinsky, S
Visscher, BR
Fahey, JL
Giorgi, JV
Dudley, J
Lee, M
Nishanian, P
Rinaldo, CR
Kingsley, LA
Kingsley, A
Mellors, J
Winkelstein, A
Munoz, A
Park, L
Gange, S
Nelson, K
Jacobson, LP
Su, S
机构
[1] WAKE FOREST UNIV, BOWMAN GRAY SCH MED, DEPT PUBL HLTH SCI, WINSTON SALEM, NC 27157 USA
[2] ALBANY MED COLL, DEPT MED, ALBANY, NY 12208 USA
[3] ALBANY MED COLL, DEPT PHARMACOL, ALBANY, NY 12208 USA
[4] UNIV PITTSBURGH, GRAD SCH PUBL HLTH, PITTSBURGH, PA 15261 USA
[5] UNIV CALIF LOS ANGELES, CTR HLTH SCI, DEPT EPIDEMIOL, LOS ANGELES, CA 90095 USA
[6] UNIV PITTSBURGH, SCH MED, PITTSBURGH, PA USA
[7] NORTHWESTERN UNIV, SCH MED, DEPT MED, CHICAGO, IL 60611 USA
[8] JOHNS HOPKINS UNIV, SCH PUBL HLTH, BALTIMORE, MD USA
[9] JOHNS HOPKINS UNIV, SCH MED, BALTIMORE, MD USA
关键词
D O I
10.7326/0003-4819-124-12-199606150-00002
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Among patients who begin receiving zidovudine during intermediate-stage human immunodeficiency virus (HIV) infection, it is unclear whether changing to combination therapy (adding didanosine or zalcitabine) or sequential monotherapy (changing to didanosine or zalcitabine) significantly improves survival. Objective: To determine, among patients who began receiving zidovudine during intermediate-stage HIV infection, the differential effects of changing to combination therapy (zidovudine with didanosine or zalcitabine) or sequential monotherapy (with didanosine or zalcitabine) or continuing zidovudine monotherapy. Patients: 1077 HIV-seropositive men in the Multicenter AIDS (acquired immunodeficiency syndrome) Cohort Study who began receiving zidovudine before an AIDS-defining illness developed. Setting: University-affiliate clinics in Baltimore, Chicago, Los Angeles, and Pittsburgh. Design: Longitudinal cohort study. Treatment groups and important prognostic variables were modeled as time-dependent covariates in Cox proportional hazards models. Measurements: Progression to AIDS and death. Results: Compared with patients receiving continued zidovudine monotherapy, patients receiving combination therapy had a 45% improvement in survival (relative risk, 0.55 [95% CI, 0.41 to 0.74; P < 0.001]) and patients who changed to sequential monotherapy had a 32% improvement in survival (relative risk, 0.68 [CI, 0.52 to 0.89; P = 0.005]). In the landmark analyses, the median prolongation of survival associated with changing therapy was, at best, 3 to 6 months. Survival curves converged at 3.5 years for the 50 cells/mm(3) disease-stage landmark, at 4.4 years for the 100 cells/mm(3) landmark, and at 4.9 years for the 150 cells/mm(3) landmark. Mortality within these periods was 100%, regardless of treatment group or landmark. Conclusions: For patients who began receiving zidovudine during intermediate-stage disease, changing to either combination therapy or sequential monotherapy was associated with a statistically significant survival benefit compared with continuation of zidovudine monotherapy. The absolute increase in survival was modest, however, and long-term survival remained poor. Simultaneous time-dependent adjustment for changes in therapy and in important prognostic variables is necessary to derive relatively unbiased estimates of treatment effects in observational studies of HIV infection.
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页码:1031 / 1038
页数:8
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