Virological Response to Initial Antiretroviral Regimens Containing Abacavir or Tenofovir

被引:7
作者
Bansi, Loveleen [1 ]
Sabin, Caroline [1 ]
Gilson, Richard [1 ]
Gazzard, Brian [2 ]
Leen, Clifford [10 ]
Anderson, Jane [3 ]
Dunn, David [4 ]
Hill, Teresa [1 ]
Fisher, Martin [11 ]
Ainsworth, Jonathan [5 ]
Pillay, Deenan [6 ]
Johnson, Margaret
Walsh, John [7 ]
Orkin, Chloe [8 ]
Easterbrook, Philippa [9 ]
Gompels, Mark [12 ]
Phillips, Andrew [1 ]
机构
[1] UCL, Sch Med, London W1N 8AA, England
[2] Chelsea & Westminster Natl Hlth Serv NHS Trust, London W1N 8AA, England
[3] Homerton Univ Hosp NHS Trust, London, England
[4] MRC, Clin Trials Unit, London, England
[5] N Middlesex Univ Hosp NHS Trust, Middlesex, England
[6] UCL, Dept Virol, London NW3 2PF, England
[7] Imperial Coll Healthcare NHS Trust, London, England
[8] Barts & London NHS Trust, London, England
[9] Kings Coll Hosp, London, England
[10] Lothian Univ Hosp NHS Trust, Edinburgh, Midlothian, Scotland
[11] Brighton & Sussex Univ Hosp NHS Trust, Brighton, E Sussex, England
[12] N Bristol NHS Trust, Bristol, Avon, England
基金
英国医学研究理事会;
关键词
HIV; COHORT;
D O I
10.1086/605024
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Patients with a baseline viral load 1100,000 copies/mL receiving abacavir (ABC) as part of the nucleoside-backbone component of their first highly active antiretroviral therapy ( HAART) regimen have been reported to have a greater failure rate than those receiving tenofovir (TDF). We analyzed short-term outcomes of the use of HAART combinations that included ABC or TDF. The mean 2-8-week change in viral load was calculated using linear regression. In total, 1136 patients started ABC, and 412 started TDF. After adjustment for baseline viral load and other factors, there was no difference in the change in viral load between the patients who started ABC and those who started TDF (0.03 [95% confidence interval, -0.07 to 0.12]) log copies/mL; P = .59). Furthermore, there was no evidence that this effect differed according to baseline viral load (P = .88 for the interaction between pre-HAART viral load and nucleoside started). Likewise, there was no difference in rates of virological failure between the 2 drugs at 24-48 weeks after starting HAART.
引用
收藏
页码:710 / 714
页数:5
相关论文
共 8 条
[1]  
COZZILEPRI A, 2001, AIDS, V15, P47
[2]   British HIV Association guidelines for the treatment of HIV-1-infected adults with antiretroviral therapy 2008 [J].
Gazzard, B. G. .
HIV MEDICINE, 2008, 9 (08) :563-608
[3]   Antiretroviral treatment of adult HIV infection - 2008 recommendations of the International AIDS Society USA panel [J].
Hammer, Scott M. ;
Eron, Joseph J., Jr. ;
Reiss, Peter ;
Schooley, Robert T. ;
Thompson, Melanie A. ;
Walmsley, Sharon ;
Cahn, Pedro ;
Fischl, Margaret A. ;
Gatell, Jose M. ;
Hirsch, Martin S. ;
Jacobsen, Donna M. ;
Montaner, Julio S. G. ;
Richman, Douglas D. ;
Yeni, Patrick G. ;
Volberding, Paul A. .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2008, 300 (05) :555-570
[4]   Clinical trials using HIV-1 RNA-based primary endpoints: Statistical analysis and potential biases [J].
Marschner, IC ;
Betensky, RA ;
DeGruttola, V ;
Hammer, SM ;
Kuritzkes, DR .
JOURNAL OF ACQUIRED IMMUNE DEFICIENCY SYNDROMES AND HUMAN RETROVIROLOGY, 1999, 20 (03) :220-227
[5]  
*PAN ANT GUID AD A, 2008, GUID US ANT AG HIV 1
[6]  
Sabin C, 2004, HIV MED, V5, P115
[7]  
Sabin CA, 2008, LANCET, V371, P1417, DOI 10.1016/S0140-6736(08)60423-7
[8]  
SAX P, 2008, 17 INT AIDS C MEX CI