Key result
Switching to paliperidone ER for lack of efficacy is linked to ~63% achieving PANSS improvement.
Why the study?
Does oral paliperidone extended release improve symptoms and functioning in adults with recently diagnosed schizophrenia previously unsuccessfully treated with other oral antipsychotics?
Observational
Yes
Does oral paliperidone extended release improve symptoms and functioning in adults with recently diagnosed schizophrenia previously unsuccessfully treated with other oral antipsychotics?
Flexibly dosed paliperidone ER provides symptomatic and functional improvement in recently diagnosed schizophrenia patients who failed prior oral antipsychotics.
May support paliperidone ER switch in recent schizophrenia after prior failure; hypothesis-generating and requires RCT confirmation before practice change.
OBJECTIVE: This study was designed to explore the efficacy and tolerability of oral paliperidone extended release (ER) in a sample of patients who were switched to flexible doses within the crucial first 5 years after receiving a diagnosis of schizophrenia. METHODS: Patients were recruited from 23 countries. Adults with nonacute but symptomatic schizophrenia, previously unsuccessfully treated with other oral antipsychotics, were transitioned to paliperidone ER (3-12 mg/day) and prospectively treated for up to 6 months. The primary efficacy outcome for patients switching for the main reason of lack of efficacy with their previous antipsychotic was at least 20% improvement in Positive and Negative Syndrome Scale (PANSS) total scores. For patients switching for other main reasons, such as lack of tolerability, compliance or 'other', the primary outcome was non-inferiority in efficacy compared with the previous oral antipsychotic. RESULTS: For patients switching for the main reason of lack of efficacy, 63.1% achieved an improvement of at least 20% in PANSS total scores from baseline to endpoint. For each reason for switching other than lack of efficacy, efficacy maintenance after switching to paliperidone ER was confirmed. Statistically significant improvement in patient functioning from baseline to endpoint, as assessed by the Personal and Social Performance scale, was observed (p < 0.0001). Treatment satisfaction with prior antipsychotic treatment at baseline was rated 'good' to 'very good' by 16.8% of patients, and at endpoint by 66.0% of patients treated with paliperidone ER. Paliperidone ER was generally well tolerated, with frequently reported treatment-emergent adverse events being insomnia, anxiety and somnolence. CONCLUSIONS: Flexibly dosed paliperidone ER was associated with clinically relevant symptomatic and functional improvement in recently diagnosed patients with non-acute schizophrenia previously unsuccessfully treated with other oral antipsychotics.
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Helldin et al. (2015) conducted an observational in Schizophrenia. Paliperidone extended release vs. Previous oral antipsychotic was evaluated on At least 20% improvement in PANSS total scores (for lack of efficacy switchers) or non-inferiority in efficacy compared with previous oral antipsychotic (for other switchers). Switching to flexibly dosed paliperidone ER resulted in 63.1% of patients who switched due to lack of efficacy achieving at least a 20% improvement in PANSS total scores.
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