Sorivudine versus acyclovir for treatment of dermatomal herpes zoster in human immunodeficiency virus-infected patients: Results from a randomized, controlled clinical trial

被引:34
作者
Gnann, JW
Crumpacker, CS
Lalezari, JP
Smith, JA
Tyring, SK
Baum, KF
Borucki, MJ
Joseph, WP
Mertz, GJ
Steigbigel, RT
Cloud, GA
Soong, SJ
Sherrill, LC
DeHertogh, DA
Whitley, RJ
机构
[1] Univ Alabama Birmingham, Div Infect Dis, Birmingham, AL 35294 USA
[2] Univ Alabama Birmingham, Ctr Comprehens Canc, Birmingham, AL 35294 USA
[3] Univ Alabama Birmingham, Childrens Hosp, Dept Pediat, Birmingham, AL 35294 USA
[4] Beth Israel Deaconess Med Ctr, Boston, MA USA
[5] Univ Calif San Francisco, Mt Zion Med Ctr, San Francisco, CA 94120 USA
[6] Univ Texas, Hlth Sci Ctr, Dept Med, Div Infect Dis, San Antonio, TX 78284 USA
[7] Univ Texas, Med Branch, Dept Immunol Microbiol, Galveston, TX 77550 USA
[8] Univ Colorado, Hlth Sci Ctr, Div Infect Dis, Denver, CO USA
[9] Infect Dis Med Grp, Oakland, CA USA
[10] Univ New Mexico, Sch Med, Dept Med, Div Infect Dis, Albuquerque, NM 87131 USA
[11] SUNY Stony Brook, Div Infect Dis, Stony Brook, NY 11794 USA
[12] Bristol Myers Squibb, Princeton, NJ USA
基金
英国惠康基金;
关键词
D O I
10.1128/AAC.42.5.1139
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The present randomized, double-blind, placebo-controlled, multicenter clinical trial was designed to compare the efficacy and tolerability of sorivudine [1-beta-D-arabinofuranosyl-E-(2-bromovinyl)uracil] and acyclovir for the treatment of dermatomal herpes tester in human immunodeficiency virus (HIV)-seropositive patients. A total of 170 HIV-seropositive adults presenting with herpes tester (confirmed by direct fluorescent-antigen testing and/or viral culture) were enrolled and randomized to receive a 10-day course of orally administered sorivudine (40 mg once daily plus acyclovir placebos) or acyclovir (800 mg five times daily plus sorivudine placebo). Patients were monitored daily to document the events of cutaneous healing, pain, tester-related complications, and drug-related adverse events. Patients were reassessed on days 21 and 28 and then once monthly for 1 year. The primary efficacy endpoint was time to the cessation of new vesicle formation. Secondary efficacy endpoints included times to other events of cutaneous healing, resolution of pain, and frequency of dissemination and tester recurrence. In a multivariate analysis, sorivudine was superior to acyclovir for reducing the times to the cessation of new vesicle formation (relative risk [RR] 1.54, 95% confidence interval [CI] = 1.00 to 2.36; P = 0.049) and total lesion crusting (RR = 1.48, 95% CI = 1.07 to 2.04; P = 0.017). In a univariate analysis, there was a trend favoring sorivudine for the cessation of new vesicle formation (median of 3 versus 4 days; P = 0.07) and a significant advantage for time to total lesion crusting (median of 7 versus 8 days; P = 0.02), The time to the resolution of tester-associated pain, the frequency of dissemination, and the frequency of tester recurrence were not different between the two treatment groups. Both drugs were well tolerated. Sorivudine is an effective drug for the treatment of herpes tester in HIV-infected patients and results in accelerated cutaneous healing when compared with acyclovir therapy.
引用
收藏
页码:1139 / 1145
页数:7
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