Randomized trial comparing saquinavir soft gelatin capsules versus indinavir as part of triple therapy (CHEESE study)

Citation
Jwtc. Stuart et al., Randomized trial comparing saquinavir soft gelatin capsules versus indinavir as part of triple therapy (CHEESE study), AIDS, 13(7), 1999, pp. F53-F58
Citations number
16
Categorie Soggetti
Immunology
Journal title
AIDS
ISSN journal
02699370 → ACNP
Volume
13
Issue
7
Year of publication
1999
Pages
F53 - F58
Database
ISI
SICI code
0269-9370(19990507)13:7<F53:RTCSSG>2.0.ZU;2-O
Abstract
Objective: To compare efficacy and tolerability of saquinavir soft gelatin capsule (SQV-SGC) formulation and indinavir, both given as part of a triple drug regimen containing zidovudine and lamivudine, in HIV-l-infected indiv iduals. Design: Randomized, open label, multicentre study. Patients: A total of 70 patients who were antiretroviral-naive and who had a CD4 cell count < 500 x 10(6)/1 and/or > 10 000 HIV RNA copies/ml plasma a nd/or HIV-related symptoms. Subjects were assigned randomly to zidovudine 2 00 mg three times per day plus lamivudine 150 mg twice per day plus either SQV-SGC 1200 mg three times per day (SQV-SGC group) or indinavir 800 mg thr ee times per day (indinavir group). Data are presented for all patients up to week 24. Results: Mean baseline CD4 cell counts (+/- SE) were 301 +/- 29 x 10(6) cel ls/l and 310 +/- 43 x 10(6) cells/l in the SQV-SCC and indinavir groups, re spectively. The log,, median baseline HIV RNA load was 5.00 copies/ml in th e SQV-SCC group and 4.98 copies/ml in the indinavir group. No difference in antiretroviral effect between the treatment arms could be demonstrated. In tention-to-treat analysis (last observation carried forward [LOCF]) at week 24 revealed that RNA levels decreased to < 50 copies/ml in 74.3% of patien ts in the SQV-SGC group and in 71.4% of the patients in the indinavir group (P = 0.78). In the on-treatment analysis the proportion of patients < 50 c opies/ml at week 24 was 88.0% in the SQV-SCC group and 84.6% in the indinav ir group (P = 0.725). Intriguingly, the mean increase of CD4 cells in the f irst 24 weeks was 162 +/- 20x10(6) cells/l in the SQV-SCC group and 89 +/- 21 x 10(6) cells/l in the indinavir group (P = 0.01), but preliminary data indicate that this difference in CD4 cell count gain may disappear after 24 weeks of treatment. Both regimens were generally well tolerated. Conclusion: During the first 24 weeks of the study, we found no difference in antiviral potency between the indinavir group and the SQV-SCC group. A s ignificantly higher CD4 response in the SQV-SGC group was observed. (C) 199 9 Lippincott Williams & Wilkins.