Therapeutic Team Leader: Psychiatry, Janssen Scientific Affairs, LLC, 1125 Trenton-Harbourton Rd-A32404, Titusville, NJ 08560
J Clin Psychiatry. 2015 May;76(5):554-61. doi: 10.4088/JCP.14m09584.
The Paliperidone Palmitate Research in Demonstrating Effectiveness (PRIDE) study compared the effects of once-monthly paliperidone palmitate with daily oral antipsychotics on treatment failure in adults with schizophrenia.
The PRIDE study is a 15-month, randomized, multicenter study (May 5, 2010, to December 9, 2013) of adult subjects with a DSM-IV diagnosis of schizophrenia and a history of incarceration. Subjects were randomly assigned to once-monthly paliperidone palmitate injections or daily oral antipsychotics (randomly assigned from 7 acceptable, prespecified oral antipsychotics) for 15 months. The primary end point was time to first treatment failure, defined as arrest/incarceration; psychiatric hospitalization; suicide; treatment discontinuation or supplementation due to inadequate efficacy, safety, or tolerability; or increased psychiatric services to prevent hospitalization. Time to first treatment failure was determined by a blinded event-monitoring board and analyzed with the Kaplan-Meier method.
In this study, 450 patients were randomly assigned, and 444 were included in the intent-to-treat population. Paliperidone palmitate was associated with significant delay in time to first treatment failure versus oral antipsychotics (hazard ratio, 1.43; 95% CI, 1.09-1.88; log rank P = .011). Observed treatment failure rates over 15 months were 39.8% and 53.7%, respectively. Arrest/incarceration and psychiatric hospitalization were the most common reasons for treatment failure in the paliperidone palmitate and oral antipsychotic groups (21.2% vs 29.4% and 8.0% vs 11.9%, respectively). The 5 most common treatment-emergent adverse events for the paliperidone palmitate treatment group were injection site pain (18.6% of subjects), insomnia (16.8%), weight increased (11.9%), akathisia (11.1%), and anxiety (10.6%).
In a trial designed to reflect real-world management of schizophrenia, once-monthly paliperidone palmitate demonstrated superiority compared to oral antipsychotics in delaying time to treatment failure.
Clinicaltrials.gov Identifier: NCT01157351.
棕榈酸帕利哌酮研究证明疗效(PRIDE)研究比较了每月一次帕利哌酮棕榈酸酯与每日口服抗精神病药治疗精神分裂症成人治疗失败的效果。
PRIDE 研究是一项为期 15 个月的随机、多中心研究(2010 年 5 月 5 日至 2013 年 12 月 9 日),纳入了符合 DSM-IV 精神分裂症诊断标准和监禁史的成年受试者。受试者被随机分配接受每月一次的棕榈酸帕利哌酮注射或每日口服抗精神病药物治疗(从 7 种可接受的预设口服抗精神病药物中随机分配),持续 15 个月。主要终点是首次治疗失败的时间,定义为逮捕/监禁;精神病住院;自杀;因疗效、安全性或耐受性差而停药或补充治疗;或增加精神科服务以预防住院。首次治疗失败时间由盲法事件监测委员会确定,并采用 Kaplan-Meier 法进行分析。
这项研究中,450 名患者被随机分配,444 名患者被纳入意向治疗人群。与口服抗精神病药相比,棕榈酸帕利哌酮显著延迟了首次治疗失败的时间(风险比,1.43;95%置信区间,1.09-1.88;对数秩检验 P =.011)。在 15 个月时,观察到的治疗失败率分别为 39.8%和 53.7%。逮捕/监禁和精神病住院是棕榈酸帕利哌酮和口服抗精神病药组中最常见的治疗失败原因(分别为 21.2%和 29.4%和 8.0%和 11.9%)。棕榈酸帕利哌酮治疗组中最常见的 5 种治疗后出现的不良事件是注射部位疼痛(18.6%的受试者)、失眠(16.8%)、体重增加(11.9%)、静坐不能(11.1%)和焦虑(10.6%)。
在一项旨在反映精神分裂症实际管理情况的试验中,每月一次的棕榈酸帕利哌酮与口服抗精神病药相比,在延迟治疗失败时间方面表现出优越性。
Clinicaltrials.gov 标识符:NCT01157351。