Cited by 377Schizophrenia research and treatmentBipolar Disorder and TreatmentTreatment of Major Depression

Efficacy and tolerability of olanzapine, quetiapine, and risperidone in the treatment of early psychosis: a randomized, double-blind 52-week comparison

McEvoy, Joseph P., Lieberman, Jeffrey A., Perkins, Diana O., Hamer, Robert M., Gu, Hongbin, Lazarus, Arthur, Sweitzer, Dennis, Olexy, Christina +2 more·2007·American Journal of Psychiatry

Abstract

OBJECTIVE: This 52-week randomized, double-blind, flexible-dose, multicenter study evaluated the overall effectiveness (as measured by treatment discontinuation rates) of olanzapine, quetiapine, and risperidone in patients early in the course of psychotic illness. METHOD: Patients were randomly assigned to treatment with olanzapine (2.5-20 mg/day), quetiapine (100-800 mg/day), or risperidone (0.5-4 mg/day) administered in twice-daily doses. Statistical analyses tested for noninferiority in all-cause treatment discontinuation rates up to 52 weeks (primary outcome measure) based on a prespecified noninferiority margin of 20%. RESULTS: A total of 400 patients were randomly assigned to treatment with olanzapine (N=133), quetiapine (N=134), or risperidone (N=133). The mean modal prescribed daily doses were 11.7 mg for olanzapine, 506 mg for quetiapine, and 2.4 mg for risperidone. At week 52, all-cause treatment discontinuation rates were 68.4%, 70.9%, and 71.4% for olanzapine, quetiapine, and risperidone, respectively. Reductions in total score on the Positive and Negative Syndrome Scale (PANSS) were similar for the three treatment groups, but reductions in PANSS positive subscale scores were greater in the olanzapine group (at 12 weeks and at 52 weeks or withdrawal from study) and the risperidone group (at 12 weeks). The most common elicited adverse events for olanzapine were drowsiness (53%), weight gain (51%), and insomnia (38%); for quetiapine, drowsiness (58%), increased sleep hours (42%), and weight gain (40%); and for risperidone, drowsiness (50%), menstrual irregularities in women (47%), and weight gain (41%). CONCLUSIONS: Olanzapine, quetiapine, and risperidone demonstrated comparable effectiveness in early-psychosis patients, as indicated by similar rates of all-cause treatment discontinuation.

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Crossref · 10.1176/ajp.2007.164.7.1050

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  • A majority of completed and ongoing trials follow the MATRICS guidelines for studying an adjunctive/cotreatment agent in a randomized, placebo-controlled trial consisting of clinically stable participants with schizophrenia.

    “In general, a majority of completed and ongoing trials follow the MATRICS guidelines17 for studying an adjunctive/cotreatment agent in a randomized, placebo-controlled trial consisting of clinically stable participants with schizophrenia.17,51–53”

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Authors
McEvoy, J. P., Lieberman, J. A., Perkins, D. O., Hamer, R. M., Gu, H., Lazarus, A., Sweitzer, D., Olexy, C., Weiden, P., & Strakowski, S. D.
Affiliations
Duke Medical Center (US)
Venue
American Journal of Psychiatry
Published
2007-07
Volume
164
Issue
7
Pages
1050-1060
ISSN
  • 0002-953X (ISSN-L)
  • 1535-7228
OpenAlex
W2156730504
Cited by
377
References
32
Citations by year
2026: 9 · 2025: 3 · 2024: 7 · 2023: 9 · 2022: 19 · 2021: 17 · 2020: 8 · 2019: 13 · 2018: 16 · 2017: 19 · 2016: 19 · 2015: 16 · 2014: 19 · 2013: 27 · 2012: 33
FWCI
22.91
Type
journal article
Language
en
Open access
closed
Locations
  • American Journal of Psychiatry (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Health Sciences › Medicine › Psychiatry and Mental health › Schizophrenia research and treatment
  • Health Sciences › Medicine › Psychiatry and Mental health › Bipolar Disorder and Treatment
  • Health Sciences › Medicine › Pharmacology › Treatment of Major Depression
Keywords
early psychosis, olanzapine, quetiapine, risperidone, antipsychotic efficacy, treatment discontinuation, non-inferiority, adverse events, weight gain, sleepiness, PANSS, atypical antipsychotics, long-term antipsychotic treatment, tolerability, menstrual irregularity, insomnia, sleep duration, bipolar disorder
MeSH terms
Quetiapine Fumarate, Olanzapine, Adolescent, Adult, Benzodiazepines, Dibenzothiazepines, Double-Blind Method, Drug Administration Schedule, Female, Humans, Male, Patient Dropouts, Psychiatric Status Rating Scales, Psychotic Disorders, Schizophrenia, Sleep Wake Disorders, Sleep Stages, Antipsychotic Agents, Weight Gain, Treatment Outcome, Risperidone

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