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
    Cameron, DW
    Heath-Chiozzi, M
    Danner, S
    Cohen, C
    Kravcik, S
    Maurath, C
    Sun, E
    Henry, D
    Rode, R
    Potthoff, A
    Leonard, J
    [J]. LANCET, 1998, 351 (9102) : 543 - 549
  • [4] Treatment of human immunodeficiency virus infection with saquinavir, zidovudine, and zalcitabine
    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
    [J]. 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
    Hammer, SM
    Squires, KE
    Hughes, MD
    Grimes, JM
    Demeter, LM
    Currier, JS
    Eron, JJ
    Feinberg, JE
    Balfour, HH
    Dayton, LR
    Chodakewitz, JA
    Fischl, MA
    [J]. 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
    Havlir, DV
    Marschner, IC
    Hirsch, MS
    Collier, AC
    Tebas, P
    Bassett, RL
    Ioannidis, JPA
    Holohan, MK
    Leavitt, R
    Boone, G
    Richman, DD
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1998, 339 (18) : 1261 - 1268
  • [7] Pharmacokinetic interactions between two human immunodeficiency virus protease inhibitors, ritonavir and saquinavir
    Hsu, A
    Granneman, GR
    Cao, GL
    Carothers, L
    El-Shourbagy, T
    Baroldi, P
    Erdman, K
    Brown, F
    Sun, E
    Leonard, JM
    [J]. CLINICAL PHARMACOLOGY & THERAPEUTICS, 1998, 63 (04) : 453 - 464
  • [8] Pharmacokinetic enhancement of inhibitors of the human immunodeficiency virus protease by coadministration with ritonavir
    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
    [J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1997, 41 (03) : 654 - 660
  • [9] Saquinavir pharmacokinetics alone and in combination with ritonavir in HIV-infected patients
    Merry, C
    Barry, MG
    Mulcahy, F
    Ryan, M
    Heavey, J
    Tjia, JF
    Gibbons, SE
    Breckenridge, AM
    Back, DJ
    [J]. AIDS, 1997, 11 (04) : F29 - F33
  • [10] The use of plasma HIV RNA as a study endpoint in efficacy trials of antiretroviral drugs
    Murray, JS
    Elashoff, MR
    Iacono-Connors, LC
    Cvetkovich, TA
    Struble, KA
    [J]. AIDS, 1999, 13 (07) : 797 - 804