The effect of treatment intensification in HIV-infection: a study comparing treatment with ritonavir/saquinavir and ritonavir/saquinavir/stavudine

被引:31
作者
Gisolf, EH
Jurriaans, S
Pelgrom, J
van Wanzeele, F
van der Ende, ME
Brinkman, K
Borst, MJ
de Wolf, F
Japour, AJ
Danner, SA
机构
[1] Univ Amsterdam, Acad Med Ctr, Natl AIDS Therapy Evaluat Ctr, Dept Internal Med, NL-1105 AZ Amsterdam, Netherlands
[2] Univ Amsterdam, Acad Med Ctr, Dept Human Retrovirol, NL-1105 AZ Amsterdam, Netherlands
[3] Inst Trop Med, B-2000 Antwerp, Belgium
[4] State Univ Ghent Hosp, B-9000 Ghent, Belgium
[5] Acad Hosp Dijkzigt, NL-3000 DR Rotterdam, Netherlands
[6] Acad Hosp, Nijmegen, Netherlands
[7] Abbott Labs, Abbott Pk, IL 60064 USA
[8] Univ Amsterdam, Acad Med Ctr, Dept Internal Med, Div Infect Dis Trop Med & Aids, NL-1105 AZ Amsterdam, Netherlands
关键词
HIV; protease inhibitors; stavudine; treatment intensification;
D O I
10.1097/00002030-200003100-00014
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Objective: To evaluate the effect of treatment with ritonavir (RTV)/saquinavir (SQV)/stavudine (D4T) or RTV/SQV alone, with treatment intensification if needed, in protease inhibitor- and D4T-naive HIV-1-infected individuals. Design: Multicentre, open-label, randomized controlled trial. Two-hundred and eight patients were randomized to receive treatment with RTV 400 mg/SQV 400 mg twice daily or RTV 400 mg/SQV 400 mg/D4T 40 mg twice daily. Intensification of study medication with reverse transcriptase inhibitors was permitted ii serum HIV-RNA remained > 400 copies/ml after 12 weeks of treatment. Follow-up of this study was 48 weeks. Results: In a strict intention-to-treat analysis, counting all dropouts as virological failures, 63% [95% confidence interval (Cl), 54-73%] of subjects in the RTV/SQV group (n = 104) reached a serum HIV-RNA ( 400 copies/ml at week 48, as compared with 69% (95% Cl, 60-78%) in the RTV/SQV/D4T group in = 104; P = 0.379). In the on-treatment analysis these percentages were 88 and 91% respectively. Thirty-one patients intensified their study medication according to the protocol (28 in the RTV/SQV group, three in the RTV/SQV/D4T group). Thirty out of 31 (97%) patients had a serum HIV-RNA ( 400 copies/ml at their last follow-up visit. Ten per cent of patients discontinued study medication due to adverse events. Conclusion: The concept of starting with a simple, potent regimen, that could be intensified if necessary, showed good virological results after 48 weeks in this study, comparable to starting with more drugs from the beginning. Longer follow-up is needed to determine the long-term efficacy of this treatment strategy. (C) 2000 Lippincott Williams & Wilkins.
引用
收藏
页码:405 / 413
页数:9
相关论文
共 16 条
[1]  
*ACTG CRIT DIV AID, 1992, TABL GRAD SEV AD ADV
[2]  
Cameron DW, 1999, AIDS, V13, P213, DOI 10.1097/00002030-199902040-00009
[3]   Randomised placebo-controlled trial of ritonavir in advanced HIV-1 disease [J].
Cameron, DW ;
Heath-Chiozzi, M ;
Danner, S ;
Cohen, C ;
Kravcik, S ;
Maurath, C ;
Sun, E ;
Henry, D ;
Rode, R ;
Potthoff, A ;
Leonard, J .
LANCET, 1998, 351 (9102) :543-549
[4]   Treatment of human immunodeficiency virus infection with saquinavir, zidovudine, and zalcitabine [J].
Collier, AC ;
Coombs, RW ;
Schoenfeld, DA ;
Bassett, RL ;
Timpone, J ;
Baruch, A ;
Jones, M ;
Facey, K ;
Whitacre, C ;
McAuliffe, VJ ;
Friedman, HM ;
Merigan, TC ;
Reichman, RC ;
Hooper, C ;
Corey, L .
NEW ENGLAND JOURNAL OF MEDICINE, 1996, 334 (16) :1011-1017
[5]   A controlled trial of two nucleoside analogues plus indinavir in persons with human immunodeficiency virus infection and CD4 cell counts of 200 per cubic millimeter or less [J].
Hammer, SM ;
Squires, KE ;
Hughes, MD ;
Grimes, JM ;
Demeter, LM ;
Currier, JS ;
Eron, JJ ;
Feinberg, JE ;
Balfour, HH ;
Dayton, LR ;
Chodakewitz, JA ;
Fischl, MA .
NEW ENGLAND JOURNAL OF MEDICINE, 1997, 337 (11) :725-733
[6]   Maintenance antiretroviral therapies in HIV-infected subjects with undetectable plasma HIV RNA after triple-drug therapy [J].
Havlir, DV ;
Marschner, IC ;
Hirsch, MS ;
Collier, AC ;
Tebas, P ;
Bassett, RL ;
Ioannidis, JPA ;
Holohan, MK ;
Leavitt, R ;
Boone, G ;
Richman, DD .
NEW ENGLAND JOURNAL OF MEDICINE, 1998, 339 (18) :1261-1268
[7]   Pharmacokinetic interactions between two human immunodeficiency virus protease inhibitors, ritonavir and saquinavir [J].
Hsu, A ;
Granneman, GR ;
Cao, GL ;
Carothers, L ;
El-Shourbagy, T ;
Baroldi, P ;
Erdman, K ;
Brown, F ;
Sun, E ;
Leonard, JM .
CLINICAL PHARMACOLOGY & THERAPEUTICS, 1998, 63 (04) :453-464
[8]   Pharmacokinetic enhancement of inhibitors of the human immunodeficiency virus protease by coadministration with ritonavir [J].
Kempf, DJ ;
Marsh, KC ;
Kumar, G ;
Rodrigues, AD ;
Denissen, JF ;
McDonald, E ;
Kukulka, MJ ;
Hsu, A ;
Granneman, GR ;
Baroldi, PA ;
Sun, E ;
Pizzuti, D ;
Plattner, JJ ;
Norbeck, DW ;
Leonard, JM .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1997, 41 (03) :654-660
[9]   Saquinavir pharmacokinetics alone and in combination with ritonavir in HIV-infected patients [J].
Merry, C ;
Barry, MG ;
Mulcahy, F ;
Ryan, M ;
Heavey, J ;
Tjia, JF ;
Gibbons, SE ;
Breckenridge, AM ;
Back, DJ .
AIDS, 1997, 11 (04) :F29-F33
[10]   The use of plasma HIV RNA as a study endpoint in efficacy trials of antiretroviral drugs [J].
Murray, JS ;
Elashoff, MR ;
Iacono-Connors, LC ;
Cvetkovich, TA ;
Struble, KA .
AIDS, 1999, 13 (07) :797-804