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under which this article appears:Bipolar
Disorder Anticonvulsants
Atypical
Neuroleptics
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Article |
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Abstract |
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 TOP Abstract IntroductionMethodResultsDiscussionReferences |
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20 for inclusion, 
12 for remission, and 15 for relapse. Analytical techniques
included mixed model repeated-measures analysis of variance for
change from baseline, Fisher’s exact test (two-tailed) for
categorical comparisons, and Kaplan-Meier estimates of time to events
of interest. RESULTS: Over 47 weeks, mean improvement in Young
Mania Rating Scale score was significantly greater for the olanzapine
group. Median time to symptomatic mania remission was significantly
shorter for olanzapine, 14 days, than for divalproex, 62 days. There
were no significant differences between treatments in the rates of
symptomatic mania remission over the 47 weeks (56.8% and 45.5%,
respectively) and subsequent relapse into mania or depression (42.3%
and 56.5%). Treatment-emergent adverse events occurring significantly
more frequently during olanzapine treatment were somnolence, dry
mouth, increased appetite, weight gain, akathisia, and high alanine
aminotransferase levels; those for divalproex were nausea and
nervousness. CONCLUSIONS: In this 47-week study of acute
bipolar mania, symptomatic remission occurred sooner and overall
mania improvement was greater for olanzapine than for divalproex, but
rates of bipolar relapse did not differ.
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Introduction |
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| TOPAbstractIntroductionMethodResultsDiscussionReferences |
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Prospective follow-up of bipolar patients has shown that the mean time to syndromal remission is approximately 6 weeks for first manic episodes. In some patients, remission may take longer (4). In a naturalistic study (4), we found that 50.0% of first-episode patients experienced syndromal remission of psychotic mania in 5.9 weeks, but there was considerable variability. At 3, 6, 12, and 24 months, 65.1%, 83.7%, 91.1%, and 97.5% of patients achieved syndromal remission, respectively. When other definitions of remission are used, the time to remission varies further. Similar rates were found in another study of first-episode bipolar illness conducted at the University of Cincinnati (5). However, as a history of previous episodes of bipolar disorder is a strong predictor of relapse (6, 7), the outcome after the first episode may differ from the outcome after multiple episodes (2).
Both divalproex (8, 9) and olanzapine (10, 11) have been shown to be efficacious in acute mania, each in two double-blind, placebo-controlled, parallel-group trials. In addition, longer-term treatment with divalproex was studied in one published double-blind, placebo-controlled, parallel-group trial (12). The lack of longer-term studies is not unusual, as there have been few trials with other medications for the maintenance of bipolar disorder (13–15).
We previously reported (16) results from a 3-week study assessing the safety and efficacy of olanzapine compared with divalproex for patients with a diagnosis of bipolar mania. Patients were randomly assigned to double-blind treatment with either olanzapine (5–20 mg/day) or divalproex (500–2500 mg/day, recommended therapeutic serum level of 50–125 µg/ml). After this initial period, the patients entered a 44-week, double-blind extension period, in which they remained in the same treatment group. We reported that olanzapine-treated patients had significantly greater improvement as shown by the Young Mania Rating Scale (17) and that the proportion of these patients who achieved protocol-defined remission was greater than that for the divalproex-treated patients. In this article we focus on improvement of mania symptoms, remission rates, time to response, and relapse rates over the entire 47-week treatment period.
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Method |
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| TOPAbstractIntroductionMethodResultsDiscussionReferences |
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The protocol was reviewed and approved by local institutional review boards at each of the 44 study sites in the United States before enrollment of any patients. After the study was thoroughly explained, each patient signed written, informed consent. Patients remained inpatients for at least the first week of double-blind treatment.
The initial dose of olanzapine was 15 mg/day, and for divalproex it was 750 mg/day, consistent with the manufacturers’ recommendations (19). The investigators made dose adjustments based primarily on clinical response but also on serum concentrations and adverse events. Patients who did not tolerate the minimum treatment dose (5 mg/day of olanzapine or 500 mg/day of divalproex) were removed from the study.
Serum concentrations were measured to evaluate whether divalproex trough levels were maintained within the targeted therapeutic range of 50–125 µg/ml. To maintain the blind, blood was also drawn from all subjects randomly assigned to olanzapine, and sham "divalproex" results were reported, as we will describe. All investigators at the clinical sites and at Lilly Research Laboratories were kept blinded to treatment assignment. Blood was drawn from all patients periodically during the study. The samples were shipped to an independent reference laboratory; a coordinator at the reference laboratory was unblinded to treatment assignment. Divalproex concentrations below 35 µg/ml were reported as "well below target level," those from 35 to 49 µg/ml were reported as "below target level," those from 126 to 150 µg/ml were reported as "above target level," and those above 150 µg/ml were reported as "well above target level." If a serum level was found to be above or below the therapeutic range, the divalproex dose was modified accordingly such that the serum level was brought back to the therapeutic range within 30 days. For each report of a serum level out of the target range that was sent for a divalproex-treated patient, a similar sham out-of-target-range report for divalproex was sent for a randomly selected olanzapine-treated patient at a different investigative site. If the investigator decided to change the medication dose on the basis of the sham divalproex serum level for a patient taking olanzapine, the increase or decrease affected only the number of placebo tablets given to that patient. This method ensured maintenance of the blind procedure.
Concomitant lorazepam was allowed throughout the 47 weeks, but use was restricted to a maximum dose of 2 mg/day, and it was not allowed within 8 hours of the administration of a symptom rating scale. Benztropine was permitted to treat extrapyramidal symptoms, up to a maximum of 6 mg/day. Throughout the study, benztropine was not allowed as prophylaxis for extrapyramidal symptoms.
Assessment
Severity of symptoms was assessed with the
11-item Young Mania Rating Scale (17),
the 21-item Hamilton Depression Rating Scale (20),
the severity of illness rating from the Clinical Global Impressions
(CGI) scale for bipolar disorder (21),
and the Positive and Negative Syndrome Scale (22).
These were administered daily during the first week, weekly from
weeks 1 to 5, biweekly from weeks 5 to 11, monthly from weeks 11 to
23, and bimonthly from weeks 23 to 47. The a priori categorical
definitions included the following. Symptomatic remission of mania
was defined as an endpoint total score on the Young Mania Rating
Scale of 12.
Symptomatic remission of mania and depression was defined as an
endpoint total mania score of 12
and a Hamilton depression scale score of 8. Syndromal remission of mania was defined
on the basis of DSM-IV criteria as having no A criterion worse
than mild in severity and no more than two B criteria rated as
mild in severity, as previously defined in the literature (4,
5,
23).
Syndromal remission of mania and depression was defined as the
preceding mania criteria plus the following depression criteria: no
DSM-IV A criteria for a major depressive episode that were worse than
mild in severity and the presence of no more than three A criteria
rated as mild, as previously suggested by Frank et al. (24).
Symptomatic relapse into an affective episode (depression, mania, or
mixed) was defined as a mania score of 15 or a depression score of 15 in a patient who previously met
the criteria for symptomatic remission. Syndromal relapse into an
affective episode was defined as achievement of syndromal remission
according to both mania and depression criteria followed by relapse
into either mania or depression. Time to remission was determined on
the basis of when the patient first met the criteria for remission.
Time to relapse was computed by prospectively examining the data
for the patients who met the criteria for remission at week 3.
Safety was monitored by assessing adverse events, laboratory values,
ECGs, vital signs, weight change, and extrapyramidal symptoms,
measured with the Simpson-Angus Rating Scale (25),
Barnes Rating Scale for Drug-Induced Akathisia (26),
and Abnormal Involuntary Movement Scale (AIMS) (27).
Adverse events that originally occurred or worsened during
double-blind therapy were considered treatment emergent and were
recorded and coded by using the Coding Symbols for Thesaurus of
Adverse Reaction Terms (COSTART) dictionary (28).
Statistical Methods
Patient data were analyzed on an
intent-to-treat basis. Patients with a baseline and at least one
postbaseline measurement were included in the analysis. Total scores
were derived from the individual items; if any single item was
missing, the total score was treated as missing. Analyses of change
from baseline in the efficacy measures were conducted by using a
mixed model repeated-measures analysis of variance (MMRM) with visit,
treatment, investigator, and visit-by-treatment interaction as
effects in the model and with the corresponding baseline score and
the interaction between baseline score and visit included as
covariates. An unstructured covariance matrix was fit to the
within-patient repeated measures. The main overall effect of
treatment was assessed, as well as the difference between treatment
groups in change from baseline to each visit, by using contrasts
within the repeated-measures model. As an additional analysis,
mean change from baseline to endpoint, with the last observation
carried forward, was examined by using ANOVA with treatment and
investigator in the model. Rates were compared in the two groups by
using Fisher’s exact test. Time to symptomatic and syndromal
remission of mania only and to both mania and depression and time to
symptomatic and syndromal recurrence of mania and depression were
analyzed by using Kaplan-Meier survival curves, and the curves were
compared by using the log-rank test. Time to discontinuation was
analyzed in a similar fashion. Treatment-emergent adverse events
(based on COSTART terms) and rates of treatment-emergent abnormally
high or low laboratory values and vital signs were compared with
Fisher’s exact test. Weight, laboratory values, and extrapyramidal
symptom ratings were analyzed by using mean change from baseline
to endpoint (last observation carried forward) in an ANOVA with
treatment and investigator in the model. In addition, the percentages
of patients gaining at least 7% of baseline body weight (last
observation carried forward) were compared by using Fisher’s
exact test. All p values were based on two-tailed tests with a
significance level of 0.05.
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Results |
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| TOPAbstractIntroductionMethodResultsDiscussionReferences |
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The disposition of the patients is shown in Table
2. A total of 125 olanzapine-treated patients and 123
divalproex-treated patients had at least one postbaseline measurement
and were included in the analysis. Patients in remission at week 3
were more likely to complete the 47-week trial (12 [20.3%] of 59
olanzapine-treated patients and 11 [26.2%] of 42 divalproex-treated
patients) than those not in remission (seven [10.6%] of 66
olanzapine-treated and nine [11.1%] of 81 divalproex-treated
patients) (p=0.01, Cochran-Mantel-Haenszel test stratified by
treatment). The numbers of subjects were 91 for olanzapine and 89 for
divalproex at week 3, 46 for olanzapine and 44 for divalproex at week
15, and 19 for olanzapine and 20 for divalproex at week 47. The
median time to discontinuation was 62 days for the olanzapine
group and 49 days for the divalproex group (log rank 
2=0.01, df=1,
p=0.93).
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There was no difference between groups in compliance. The patients were highly compliant with study medication, as assessed by pill counts (90.6% for olanzapine and 89.9% for divalproex). The mean modal dose for the olanzapine-treated patients was 16.2 mg/day (SD=4.9), and the mean modal dose for the divalproex-treated patients was 1584.7 mg/day (SD=618.1). The mean valproate blood levels after 3, 7, 11, and 47 weeks of treatment were 83.9 µg/ml (SD=32.1), 72.5 µg/ml (SD=33.6), 64.1 µg/ml (SD=34.3), and 58.2 µg/ml (SD=30.8), respectively. The percentages of patients with blood levels of 50 µg/ml or higher were 88.3%, 78.1%, 71.4%, and 61.9%, respectively, after 3, 7, 11, and 47 weeks of treatment. The mean daily doses were 1554.1 mg (SD=491.4) at week 3, 1708.0 mg (SD=541.5) at week 7, 1716.8 mg (SD=517.1) at week 11, and 1500.5 mg (SD=579.7) at week 47.
Efficacy
Rating scale
scores
Differences in the total score on the Young Mania
Rating Scale were examined by using an MMRM. The olanzapine-treated
patients experienced a significantly greater reduction in
least-squares mean score than the divalproex-treated patients; the
difference between groups in the reduction averaged 2.38 points
(SE=0.76) over the trial (F=9.77, df=1, 88, p=0.002). The
improvement with olanzapine was significantly superior at all visits
between weeks 2 and 15, inclusive, and at week 23 (Figure
1). However, the differences in improvement narrowed later in the
study, and there were no significant differences between
treatments from week 30 to week 47. An analysis of the change from
baseline to endpoint (last observation carried forward up to week
47) detected a statistically significant difference between the
groups (olanzapine: mean=–15.38, SD=10.17; divalproex:
mean=–12.50, SD=11.51) (F=5.43, df=1, 218, p=0.03).
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In the MMRM, the improvement in mean Hamilton depression score for the olanzapine-treated patients was greater by 1.19 points (SE=0.65) than that of the divalproex-treated patients, but the difference was not statistically significant (F=3.39, df=1, 107, p=0.07). An analysis of the change from baseline to endpoint in the Hamilton depression scale score, with the last observation carried forward, indicated no significant difference between groups (olanzapine: mean=–3.78, SD=8.92; divalproex: mean=–1.59, SD=8.22) (F=3.25, df=1, 216, p=0.08).
No significant differences between groups were found in the total score on the Positive and Negative Syndrome Scale according to MMRM (F=0.07, df=1, 106, p=0.80) or change from baseline to endpoint with the last observation carried forward (olanzapine: mean=–12.11, SD=19.69; divalproex: mean=–8.87, SD=19.36) (F=1.37, df=1, 216, p=0.25). No significant differences between groups were found in the CGI severity of illness with MMRM (F=2.59, df=1, 119, p=0.11) or the change from baseline to endpoint with the last observation carried forward (olanzapine: mean=–1.98, SD=1.42; divalproex: mean=–1.70, SD=1.53) (F=3.58, df=1, 217, p=0.06).
Symptomatic and syndromal remission of
mania
The median time to symptomatic remission of mania
(defined as a score of 12 or less on the Young Mania Rating Scale)
was significantly shorter for the olanzapine-treated patients (14
days) than for those treated with divalproex (62 days) (log rank 2=3.96, df=1,
p=0.05). At 47 weeks (last observation carried forward), the
rates of symptomatic mania remission were 56.8% and 45.5% for
the olanzapine and divalproex groups, respectively (Fisher’s
exact p=0.10).
The median times to syndromal remission of mania were 28 and 109
days for the olanzapine- and divalproex-treated groups, respectively
(log rank 2=6.63,
df=1, p=0.01). The syndromal remission rates at 47 weeks were 50.8%
for olanzapine versus 38.2% for divalproex (Fisher’s exact
p=0.06).
Symptomatic and syndromal remission of both mania and
depression
The times to symptomatic remission of mania and
depression were similar for olanzapine (25th percentile=14 days) and
divalproex (25th precentile=13 days) (2=0.03, df=1, p=0.86). At 47
weeks (last observation carried forward), the rates of
symptomatic remission of both mania and depression were 30.9% for
both the olanzapine and divalproex groups (Fisher’s exact
p=1.00).
The times to syndromal remission of both mania and depression did
not differ significantly between groups: the 25th percentile was 7
days for olanzapine and 34 days for divalproex (2=0.25, df=1, p=0.62).
Likewise, the rates of syndromal remission at 47 weeks were similar:
29.8% for olanzapine and 27.6% for divalproex (Fisher’s exact
p=0.78).
Symptomatic recurrence of any affective
episode
There was no statistically significant difference in
time to symptomatic recurrence of an affective episode
(depression, mania, or mixed) between the olanzapine- and
divalproex-treated groups (2=0.22, df=1, p=0.64) (25th percentile for both
groups=27 days). Symptomatic recurrence of an affective episode
occurred in 14 (42.4%) of 33 olanzapine-treated patients and 13
(56.5%) of 23 divalproex-treated patients (Fisher’s exact
p=0.42). Of the 14 olanzapine-treated patients experiencing
recurrence, eight experienced depression, five experienced mania, and
one experienced a mixed episode. Of the 13 divalproex-treated
patients experiencing recurrence, six experienced depression, four
experienced mania, and three experienced mixed episodes.
Syndromal recurrence of any affective
episode
There was no statistically significant difference in
the times to syndromal recurrence of an affective episode between
the olanzapine- and divalproex-treated groups (2=0.70, df=1, p=0.41)
(the medians for olanzapine and divalproex were 14 and 42 days,
respectively). Syndromal recurrence of an affective episode
occurred in 20 (64.5%) of 31 olanzapine-treated patients and 13
(65.0%) of 20 divalproex-treated patients (Fisher’s exact
p=1.00).
Relation of valproate serum concentration to
outcome
In an examination of patients whose valproate
concentrations were measured at 3 weeks, a median split of patients
by valproate concentration (valproate measurements were available for
77 patients; median concentration=82 µg/ml) showed no difference
in the percentage of patients in remission at week 3 (last
observation carried forward analysis). Of the 38 patients with "high"
concentrations (above 82 µg/ml), 42.1% (N=16) were in remission
compared to 38.5% (N=15) of the 39 patients with "low"
concentrations (less than or equal to 82 µg/ml) (Fisher’s exact
test, p=0.82). Similarly, there was no difference in the remission
rates at endpoint (last observation carried forward up to week
47) between the patients with high concentrations (57.9%, N=22)
and those with low concentrations (56.4%, N=22) (Fisher’s exact
test, p=1.00). In an examination of completion rates, there was again
no significant difference between the patients with high
concentrations (21.1%, N=8) and those with low concentrations (25.6%,
N=10) (Fisher’s exact test, p=0.79).
A secondary analysis was also conducted to compare the remission
rate of the olanzapine-treated patients to that of the only 91
(of 123) divalproex-treated patients with valproate blood levels at
or above the therapeutic range (50 µg/ml) at week 1 of treatment. Fourteen patients were
dropped from this analysis because their blood levels were below 50
µg/ml, and for 18 patients valproate levels were not measured at
week 1. The rates of symptomatic remission of mania at week 47
(last observation carried forward) were 56.8% and 51.6% for the
olanzapine- and divalproex-treated patients, respectively
(Fisher’s exact test, p=0.49). The median time to symptomatic mania
remission was 27 days for the divalproex patients with therapeutic
blood concentrations, compared to the 14 days for olanzapine
(log rank 2=2.43, df=1, p=0.12). For syndromic remission of mania
at week 47 (last observation carried forward), 44.0% of
divalproex-treated patients met the criteria compared to 50.8% of
olanzapine-treated patients (Fisher’s exact test, p=0.34). The median
time to remission remained 28 days for olanzapine and 109 days
for divalproex (log rank 2=4.66, df=1, p=0.04).
Finally, the total score on the Young Mania Rating Scale and the improvement from baseline in patients with valproate blood concentrations less than 50 µg/ml at week 3, 7, 11, or 47 did not significantly differ from those of the patients with valproate blood concentrations of 50 µg/ml or higher. In fact, at three of the four assessments (weeks 3, 7, and 47), the results were numerically better in the group with concentrations below 50 µg/ml.
Safety
A total of 31 (24.8%) of the 125 olanzapine
patients and 25 (19.8%) of the 126 divalproex patients discontinued
study participation because of an adverse event (Fisher’s exact test,
p=0.37). Treatment-emergent adverse events (as reported by the
investigator) occurring more frequently during treatment with
olanzapine (Fisher’s exact test, p<0.05) were somnolence, dry
mouth, increased appetite, weight gain, akathisia, and elevated liver
function test results (alanine aminotransferase). Among the
patients receiving divalproex, nausea, nervousness, rectal
disorder, and manic reaction were more common (p<0.05). While the
COSTART term "manic reaction" was listed significantly more often
for divalproex- than olanzapine-treated patients, this
occurrence likely is related to efficacy rather than being an adverse
event. Table
3 shows adverse events that were statistically different between
groups or occurred in at least 10% of the patients in either
treatment group. For treatment-emergent abnormally high laboratory
values at endpoint, there was a statistically significant difference
for alanine aminotransferase (5.1% for olanzapine versus 0.0% for
divalproex) (Fisher’s exact test, p=0.03). There were two other
significantly different treatment-emergent abnormally low laboratory
values at endpoint: albumin (1.8% for olanzapine and 8.3% for
divalproex) (Fisher’s exact test, p=0.04) and platelets (0.0% for
olanzapine and 6.2% for divalproex) (Fisher’s exact p=0.007).
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There were no significant differences between the olanzapine and divalproex groups in the mean change in extrapyramidal symptoms from baseline to endpoint, according to mean scores on the AIMS (–0.31 [SD=2.09] and –0.13 [SD=1.38] for olanzapine and divalproex, respectively) (F=0.87, df=1, 217, p=0.36), Simpson-Angus Rating Scale (0.16 [SD=2.17] and –0.31 [SD=2.44]) (F=2.39, df=1, 211, p=0.13), and Barnes Rating Scale for Drug-Induced Akathisia (–0.25 [SD=0.95] and –0.22 [SD=1.00]) (F=0.02, df=1, 211, p=0.89).
The patients in the olanzapine group had a significantly greater mean weight gain than those in the divalproex group according to an MMRM: 2.79 kg (SE=0.32) versus 1.22 kg (SE=0.32) (F=12.03, df=1, 127, p<0.001). Weight gain was significantly greater for the olanzapine patients from day 3 through week 15, inclusive; however, from weeks 19 through 47, there were no significant differences between groups in weight gain from baseline. Four olanzapine-treated patients dropped out because of weight gain, one each at weeks 3, 4, 19, and 39. At endpoint (last observation carried forward), 23.6% (N=29) of 123 olanzapine patients and 17.9% (N=22) of 123 divalproex patients had gained at least 7% of their baseline weight (Fisher’s exact test, p=0.35).
There was a significantly greater increase in cholesterol level among the olanzapine patients than among those treated with divalproex; the mean change from baseline to endpoint was 9.68 mg/dl for olanzapine (SD=34.13) and –2.33 mg/dl for divalproex (SD=32.73) (F=7.43, df=1, 205, p=0.007). There was no significant difference between groups in glucose concentration in a nonfasting state; the mean change from baseline to endpoint was 0.03 mmol/liter (SD=1.80) for olanzapine and –0.15 mmol/liter (SD=1.59) for divalproex (F=1.14, df=1, 205, p=0.29). The groups did not differ in the incidence of treatment-emergent abnormally high levels of cholesterol (olanzapine: one of 118, or 0.8%; divalproex: none of 115) (Fisher’s exact test, p=1.00) or glucose (olanzapine: none of 113; divalproex: none of 114) (Fisher’s exact test, p=1.00).
The mean change from baseline to endpoint in the Fridericia-corrected QT interval was 7.97 msec (SD=21.36) for 104 olanzapine-treated patients and –3.06 (SD=24.92) for 101 divalproex-treated patients (F=10.16, df=1, 175, p=0.002). We defined a potentially clinically significant change in QTc interval for men as from <430 msec at baseline to >430 at any point during the trial. For women we defined clinically significant change as an increase from <450 msec at baseline to >450 during the trial. Two (2.0%) of 102 olanzapine patients and two (2.1%) of 96 divalproex patients experienced such increases (Fisher’s exact test, p=1.00). Across treatment groups, no man experienced a QTc higher than 450 msec and no women experienced a QTc higher than 470 msec, other common cutoffs reported in the literature.
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Discussion |
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| TOPAbstractIntroductionMethodResultsDiscussionReferences |
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The study was designed to examine short-term and continued antimanic treatment effects, but it also allowed some exploration of relative efficacy for depressive symptoms and relapse prevention. Mean improvement in the score on the Hamilton depression scale was nonsignificantly greater for the olanzapine-treated patients. Interpretation of these findings is limited by the heterogeneity of the baseline Hamilton depression ratings (range=1–34) and variability in both groups over time. Comparative efficacy for relapse prevention would be better studied in a trial that starts with patients in stable remission. Several features of the current trial limit interpretation of the findings on relapse. For example, there are differences between the groups in the number of patients who achieved remission and the speed with which they did so. The time between ratings increased as the study progressed, such that relapse could be more efficiently captured and dated in earlier phases of the trial. The lengthening intervals between visits may have reduced overall clinical contact, perhaps contributing to patient dropout. The overall high dropout rate limits the power to detect differences in relapse. This trial failed to demonstrate a difference between treatments in time to relapse, but further study is warranted.
The mean valproate blood concentration in our study at 3 weeks was comparable to that reported by Bowden et al. (12) at 4 weeks: 83.9 versus 84.8 µg/ml, respectively. Findings on safety and tolerability were in accord with previously published findings for both agents (8, 9, 11, 12, 16, 29). The rates of study discontinuation for adverse events were similar for olanzapine and divalproex (24.8% and 19.8%, respectively). The most common adverse events for olanzapine were somnolence, depression, dry mouth, headache, weight gain, and asthenia. For divalproex, they were nausea, depression, headache, somnolence, nervousness, and pain. Weight gain was significantly greater for the olanzapine-treated patients. Generally, the courses of weight gain for the two medications appear to reflect those observed previously in different study groups. Patients with schizophrenia who gain weight while taking olanzapine are likely to have the most rapid increase in the first month, with stabilization late in the first year of treatment (30). Weight gain during treatment with divalproex appears to follow a more gradual pattern, such as that in a recently reported epilepsy clinical trial (31). Two laboratory measures increased more with olanzapine. First, the patients in that group had a greater mean increase in cholesterol. The second increased laboratory measure was alanine aminotransferase. This increase in the olanzapine-treated patients in this trial has been seen in other studies (32); it is typically observed early in treatment and is transient in nature.
A significant difference was found between the QTc intervals of the olanzapine- and divalproex-treated patients. The observed increase in the olanzapine-treated patients (7.97 msec) was greater than in other clinical trials (33, 34). The divalproex-treated patients had a mean QTc decrease of 3.06 msec. However, this difference is of unclear clinical significance because the treatment groups did not differ in the frequency of treatment-emergent QTc intervals greater than clinically important cutoffs.
There are limitations in the present study. First, dosing was adjusted at the discretion of the clinical investigator within large ranges (olanzapine: 5–20 mg/day; divalproex: 500–2500 mg/day) on the basis of response and tolerability. Therefore, it is likely that a proportion of divalproex patients had valproate blood concentrations below the therapeutic range at each visit. This proportion is probably higher than would have occurred if the study had compelled upward dose titration. Further, olanzapine was initially administered at 15 mg/day (a therapeutic dose for most patients), while divalproex was started at 750 mg/day (a subtherapeutic dose for most patients) with gradual titration upward. This dosing strategy followed the divalproex labeling instructions but may have given the olanzapine-treated group a slight early advantage in time to response. The flexible dosing scheme used in this study has the advantage of reflecting actual clinical practice, at least as represented by these investigators, but cannot directly address whether different dosing requirements might have changed the outcome; for instance, one previous divalproex trial (8) did apparently compel upward titration, if tolerated, even for patients with good clinical responses to lower doses. On the other hand, despite the differences in dosing, the two available comparisons of olanzapine and divalproex for acute mania (16, 29) show similar numeric differences between treatments in mean improvement on the 11-item Mania Rating Scale (29) or the 11-item Young Mania Rating Scale (16).
Second, the valproate concentrations were not reported as precise numbers but as broader ranges (e.g., "above target level" or "well above target level"). Because the study was blinded and included sham level reporting for the olanzapine-treated patients, this manner of reporting concentrations was not likely to have biased results, but it did limit the ability of the investigators to fine-tune their dosing and specifically may have decreased their comfort in prescribing doses that would result in blood levels above the target range as an attempt to maximize response. Late in the current study, the mean divalproex dose approached the lower end of the conventional range. It is possible that some patients at the lower end of the dose range may have been there because they were doing well and the physicians did not feel compelled to increase their doses. It is interesting that an analysis at week 3 showed no relationship between valproate blood concentration and either completion or remission. Further, no significant difference in mean total score on the Young Mania Rating Scale or in improvement from baseline was found between the divalproex patients with valproate blood concentrations below therapeutic levels and those with concentrations at or above those levels.
A third limitation of the study is that most of the patients withdrew from the study before completing 47 weeks of treatment. In fact, 31.2% of the olanzapine patients and 35.7% of the divalproex patients discontinued the study during the initial 3-week phase; of those entering the 44-week maintenance phase, 77.9% of the olanzapine-treated and 75.3% of the divalproex-treated patients left the study. High discontinuation rates in long-term studies of bipolar disorder are not unusual and underscore the difficulty of maintaining patients with bipolar disorder, at least those who have just been discharged on a monotherapy regimen after hospitalization for a manic episode. Bowden et al. (12) reported a dropout rate of 62% of patients treated with divalproex and 76% of patients treated with lithium for 52 weeks. While these are lower than the rates in the current study, it should be noted that the patients in the Bowden et al. study were required to meet criteria for stable recovery before being randomly assigned to maintenance treatments. In that study (12), approximately 35% of the patients in the open-label stabilization phase did not meet those criteria, often because of inadequately controlled manic symptoms. In our study, patients who achieved remission at the end of the acute phase were more likely to complete the present study than were patients who did not achieve remission.
A fourth limitation of the study was that the patients were generally severely ill; the mean baseline total score on the Young Mania Rating Scale was 27.7, most patients had a large number of prior episodes (93.6% had more than three previous manic, depressed, or mixed episodes at study entry), and a large proportion (57.4%) had a rapid cycling course. Therefore, our results may not generalize to less severely ill patients encountered in nonacademic clinical settings.
During this 47-week, randomized, double-blind trial for acute mania in which flexibly dosed olanzapine and divalproex were compared, olanzapine produced a faster improvement than divalproex in symptoms of mania as rated by the Young Mania Rating Scale. Compared to the previously reported first 3 weeks of treatment, longer treatment was associated with further improvement in both groups. Of the a priori clinically meaningful categorizations defining remission and response, olanzapine was superior for syndromal remission of mania. For both olanzapine and divalproex, symptomatic remission appeared earlier than syndromic remission. However, remission by both symptomatic and syndromic definitions was significantly more rapid for the olanzapine-treated patients, but the differences in remission rates between groups later in the trial were nonsignificant. There were similar rates of discontinuation due to adverse events with the two treatments, although the pattern of the most common adverse events differed between the groups. Olanzapine was associated with more weight increase early in treatment, but weight increases did not differ significantly between groups in patients who remained in treatment longer. Although the primary efficacy outcome of this trial favored olanzapine, both olanzapine and divalproex demonstrated efficacy for bipolar mania. In selecting pharmacological treatment, the clinician should consider both safety and efficacy as well as patient-specific considerations.
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under which this article appears:Bipolar
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