Background: We sought to identify baseline predictors of response to c
lozapine. Methods: Data were from a 15-site randomized clinical trial
comparing clozapine and haloperidol in hospitalized patients with refr
actory Schizophrenia (n = 423). Three-month outcomes were analyzed wit
h the full sample (n = 368 due to attrition). Because of crossovers, a
nalyses of 12-month outcomes were conducted with crossovers excluded (
n = 291). Clinical predictors included age, I-ace, diagnosis (current
substance abuse, paranoid subtype of schizophrenia, or depressive synd
rome), severity of symptoms, quality of life, age at onset of schizoph
renia, extrapyramidal symptoms, and VA compensation payment. Multiple
regression analysis was used to examine the interaction of treatment c
ondition and each of these variables in predicting outcomes for sympto
ms, quality of life, side effects, and days hospitalized. Results: Pat
ients with higher quality of life at baseline (p = .04) and higher sym
ptoms (p = .02) had relatively smaller declines in hospital days at 6
months. In the 12-month sample patients with higher levels of symptoms
had greater symptom reductions at 12 months (p = .03) and greater imp
rovement in quality of life (p = .004). Conclusions: Although high lev
els of symptoms were associated with greater improvement on clozapine,
these findings are not robust enough to suggest that any specific, cl
inically defined subgroup of refractory patients should be preferentia
lly targeted for clozapine treatment. (C) 1998 Society of Biological P
sychiatry.