Role of structured treatment interruption before a 5-drug salvage Antiretroviral regimen:: The Retrogene study

被引:54
作者
Ruiz, L
Ribera, E
Bonjoch, A
Romeu, J
Martinez-Picado, J
Paredes, R
Díaz, M
Marfil, S
Negredo, E
García-Prado, JG
Tural, C
Sirera, G
Clotet, B
机构
[1] Univ Autonoma Barcelona, Retrovirol Lab, IrsiCaixa Fdn, Hosp Germans Trias & Pujol, Barcelona 08916, Spain
[2] Univ Autonoma Barcelona, Lluita SIDA FDN, Hosp Germans Trias & Pujol, Barcelona 08916, Spain
[3] Hosp Gen Valle Hebron, Barcelona, Spain
关键词
PROTEASE INHIBITOR THERAPY; VIRUS TYPE-1 POPULATIONS; VIROLOGICAL FAILURE; HIV-1-INFECTED PATIENTS; INFECTED PATIENTS; RESISTANT HIV-1; SAQUINAVIR; EFAVIRENZ; RITONAVIR; EFFICACY;
D O I
10.1086/378411
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
We evaluated the efficacy of a 5-drug salvage regimen, preceded by a 12-week, structured treatment interruption (STI), in 46 multidrug-treated, human immunodeficiency virus type 1-infected patients with detectable viremia. Patients were randomly assigned to receive a 5-drug salvage regimen immediately (noninterruption [NI] group; patients) or after 12 weeks of STI (interruption [I] group; n = 22 patients). At week 48, 45% of patients in the I group and 46% of patients in the NI group had virus loads <50 HIV-1 RNA copies/mL (P =.619). No differences in CD4 cell counts were seen between groups at week 48 (P = .734). A complete reversion to wild-type genotype was detected in 35% of patients in the I group, but this phenomenon did not affect the virological response. The only overall baseline factor associated with ensuing virus suppression was a lower number of nucleoside reverse-transcriptase inhibitor - resistant mutations ( relative risk, 0.66; 95% confidence interval, 0.47 - 0.93; P = .021). A prior STI seems to confer no additional benefit to subsequent virological or immunological outcomes of a salvage regimen.
引用
收藏
页码:977 / 985
页数:9
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