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

  • J W Cohen Stuart
  • , R Schuurman
  • , D M Burger
  • , P P Koopmans
  • , H G Sprenger
  • , J R Juttmann
  • , C Richter
  • , P L Meenhorst
  • , R M Hoetelmans
  • , F P Kroon
  • , B Bravenboer
  • , D Hamann
  • , C A Boucher
  • , J C Borleffs

Research output: Contribution to journalArticleAcademicpeer-review

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-1-infected individuals.

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)/I and/or > 10000 HIV RNA copies/ml plasma and/or HIV-related symptoms. Subjects were assigned randomly to zidovudine 200 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 three 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) cells/l and 310 +/-43 x 10(6) cells/l in the SQV-SGC and indinavir groups, respectively. The log10 median baseline HIV RNA load was 5.00 copies/ml in the SQV-SGC group and 4.98 copies/ml in the indinavir group. No difference in antiretroviral effect between the treatment arms could be demonstrated. Intention-to-treat analysis (last observation carried forward [LOCF]) at week 24 revealed that RNA levels decreased to < 50 copies/ml in 74.3% of patients 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 copies/ml at week 24 was 88.0% in the SQV-SGC group and 84.6% in the indinavir group (P = 0.725). Intriguingly, the mean increase of CD4 cells in the first 24 weeks was 162+/-20 x 10(6) cells/l in the SQV-SGC 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-SGC group. A significantly higher CD4 response in the SQV-SGC group was observed.

Original languageEnglish
Pages (from-to)F53-8
JournalAIDS (London, England)
Volume13
Issue number7
DOIs
Publication statusPublished - 7 May 1999

Keywords

  • Adult
  • Anti-HIV Agents/therapeutic use
  • CD4 Lymphocyte Count
  • Capsules/administration & dosage
  • Drug Therapy, Combination
  • Female
  • Gelatin
  • HIV Infections/drug therapy
  • HIV Protease Inhibitors/therapeutic use
  • HIV-1/drug effects
  • Humans
  • Indinavir/administration & dosage
  • Lamivudine/therapeutic use
  • Male
  • Middle Aged
  • RNA, Viral/blood
  • Reverse Transcriptase Inhibitors/therapeutic use
  • Saquinavir/administration & dosage
  • Treatment Outcome
  • Zidovudine/therapeutic use

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