NIMH Study To Guide Treatment Choices for Schizophrenia
(Sept. 19, 2005) -- A large study funded by NIH's National Institute of Mental Health (NIMH)
provides, for the first time, detailed information comparing the effectiveness
and side effects of five medications — both new and older medications — that are
currently used to treat people with schizophrenia. Overall, the medications were
comparably effective but were associated with high rates of discontinuation due
to intolerable side effects or failure to adequately control symptoms. One new
medication, olanzapine (Zyprexa), was slightly better than the other drugs but also was
associated with significant weight-gain and metabolic changes. Surprisingly, the
older, less expensive medication used in the study generally performed as well
as the newer medications. The study, which included more than 1,400 people,
supplies important new information that will help doctors and patients choose
the most appropriate medication according to the patients' individual needs. The
study results are published in the September 22 issue of the New England
Journal of Medicine.
"The study has vital public health implications because it provides doctors
and patients with much-needed information comparing medication treatment
options," said NIMH Director Thomas R. Insel, M.D. "It is the largest, longest,
and most comprehensive independent trial ever done to examine existing therapies
for this disease."
Schizophrenia, which affects 3.2 million Americans, is a chronic, recurrent
mental illness, characterized by hallucinations, delusions, and disordered
thinking. The medications used to treat the disorder are called antipsychotics.
Previous studies have demonstrated that taking antipsychotic medication is far
more effective than taking no medicine, and that taking it consistently is
essential to the long-term treatment of this severe, disabling disorder.
Although the medications alone are not sufficient to cure the disease, they are
necessary to manage it.
In the $42.6 million CATIE (Clinical Antipsychotic Trials of Intervention
Effectiveness) trial, researchers directly compared an older medication (perphenazine),
available since the 1950s, to four newer medications (olanzapine, quetiapine,
risperidone, and ziprasidone), introduced in the 1990s. The purpose of the study
was to learn whether there are differences among the newer medications and
whether the newer medications hold significant advantages over the older
medications; these newer medications known as atypical antipsychotics, cost
roughly 10 times as much as the older medications.
The size and scope of the trial, with more than 1,400 participants at 57
sites around the country, its 18-month duration, and its inclusion of a wide
range of patients in a variety of treatment settings ensure that the findings
are reliable and relevant to the 3.2 million Americans suffering from
schizophrenia.
At the beginning of the study, patients were randomly assigned to receive one
of the five medications. Almost three quarters of patients switched from their
first medication to a different medication. The patients started on olanzapine
were less likely to be hospitalized for a psychotic relapse and tended to stay
on the medication longer than patients taking other medications. However,
patients on olanzapine also experienced substantially more weight gain and
metabolic changes associated with an increased risk of diabetes than those study
participants taking the other drugs.
Contrary to expectations, movement side effects (rigidity, stiff movements,
tremor, and muscle restlessness) primarily associated with the older
medications, were not seen more frequently with perphenazine (the drug used to
represent the class of older medications) than with the newer drugs. The older
medication was as well tolerated as the newer drugs and was equally effective as
three of the newer medications. The advantages of olanzapine — in symptom
reduction and duration of treatment — over the older medication were modest and
must be weighed against the increased side effects of olanzapine.
Thus, taken as a whole, the newer medications have no substantial advantage
over the older medication used in this study. An important issue still to be
considered is individual differences in patient response to these drugs.
Several factors, such as adequacy of symptom relief, tolerability of side
effects, and treatment cost influence a person's willingness and ability to stay
on medication.
"There is considerable variation in the therapeutic and side effects of
antipsychotic medications. Doctors and patients must carefully evaluate the
tradeoffs between efficacy and side effects in choosing an appropriate
medication. What works for one person may not work for another," said Jeffrey
Lieberman, M.D., CATIE's Principal Investigator and Chair of The Department of
Psychiatry, Columbia University and Director of the New York State Psychiatric
Institute.
The CATIE study was led by Lieberman, and co-Principal Investigators Scott
Stroup, M.D. (University of North Carolina at Chapel Hill), and Joseph McEvoy,
M.D. (Duke University). CATIE was carried out by researchers at 57 sites across
the country, including private and public mental health clinics, Veteran's
Health Administration Medical Centers, and University Medical Centers, where
people with schizophrenia received their usual care.
This New England Journal of Medicine article is the first to report outcomes
from the CATIE schizophrenia trial, and addresses many of the primary questions
from the study. Future reports will address a multitude of topics (e.g.,
cost-effectiveness of the medications, quality of life, predictors of response)
and will provide a more detailed picture of the interaction between patient
characteristics, medication, and outcomes. The information from the CATIE study
will inform new approaches for improving outcomes in schizophrenia.
CATIE is part of an overall NIMH effort to conduct "practical" clinical
trials that address public health issues important to those persons affected by
major mental illnesses in real world settings.
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Importance of the CATIE Study
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Reviewed: 03/2006
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