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帕利哌酮长效注射剂治疗青少年精神分裂症的疗效和安全性:一项随机、双盲研究。

Efficacy and safety of paliperidone extended release in adolescents with schizophrenia: a randomized, double-blind study.

机构信息

Janssen Research and Development, LLC, Titusville, NJ.

Janssen Research and Development, LLC, Titusville, NJ.

出版信息

J Am Acad Child Adolesc Psychiatry. 2015 Feb;54(2):126-137.e1. doi: 10.1016/j.jaac.2014.11.009. Epub 2014 Nov 25.

Abstract

OBJECTIVE

To evaluate the efficacy, safety, and tolerability of paliperidone extended release (ER) relative to aripiprazole in adolescent schizophrenia.

METHOD

In this multicenter, double-blind, phase 3 study (screening [≤3 weeks], with an acute treatment period [8 weeks] and a maintenance period [18 weeks]), adolescents (12-17 years old) with schizophrenia (DSM-IV diagnosis; Positive and Negative Symptom Score [PANSS] total score 60-120) were randomized (1:1) to once-daily paliperidone ER (6 mg per day [days 1-7], flexibly dosed 3, 6, or 9 mg per day from week 2 to end of study [EOS]), or to aripiprazole (2 mg per day [days 1 and 2], 5 mg per day [days 3 and 4], 10 mg per day [days 5-7], flexibly dosed 5, 10, or 15 mg per day [week 2 to EOS]).

RESULTS

Overall, 76% of enrolled patients (174/228) completed the study (paliperidone ER, 75% [85/113]; aripiprazole, 77% [89/115]). There was no significant difference in change in PANSS total scores from baseline to day 56 (primary endpoint) (paliperidone ER versus aripiprazole, -19.3 [13.80] versus -19.8 [14.56], p = .935); responders, 67.9% versus 76.3%, p = .119) and day 182 (-25.6 [16.88] versus -26.8 [18.82], p = .877; responders, 76.8% versus 81.6%, p = .444). All secondary endpoints (maintenance of clinical stability, change in PANSS-negative symptoms, Clinical Global Impression-Severity, and Personal and Social Performance scores) were similar in both treatment groups. The most common (>10% patients) treatment-emergent adverse events for paliperidone ER were akathisia, headache, somnolence, tremor, and weight gain, and for aripiprazole were worsening of schizophrenia and somnolence. Extrapyramidal symptoms including dystonia and hyperkinesia occurred in >2% in paliperidone ER-treated versus aripiprazole-treated patients.

CONCLUSION

Paliperidone ER did not demonstrate superior efficacy to aripiprazole in treating adolescent schizophrenia. Both drugs showed clinically meaningful improvements in symptom and functional measurements and were generally tolerable. Clinical Trial Registration Information-An Efficacy and Safety Study of Extended-Release (ER) Paliperidone in Adolescent Participants With Schizophrenia; http://clinicaltrials.gov; NCT01009047.

摘要

目的

评估帕利哌酮长效制剂(ER)相对于阿立哌唑在青少年精神分裂症中的疗效、安全性和耐受性。

方法

这是一项多中心、双盲、3 期研究(筛选期[≤3 周],包括急性治疗期[8 周]和维持期[18 周]),招募了符合 DSM-IV 诊断标准的青少年精神分裂症患者(12-17 岁;阳性和阴性症状量表[PANSS]总分 60-120),将其随机分为 1:1 组,分别接受每日一次帕利哌酮 ER(6 毫克/天[第 1-7 天],第 2 周到研究结束[EOS]时灵活剂量 3、6 或 9 毫克/天)或阿立哌唑(2 毫克/天[第 1 和 2 天],5 毫克/天[第 3 和 4 天],10 毫克/天[第 5-7 天],第 2 周到 EOS 时灵活剂量 5、10 或 15 毫克/天)。

结果

共有 76%的入组患者(174/228)完成了研究(帕利哌酮 ER 组,75%[85/113];阿立哌唑组,77%[89/115])。从基线到第 56 天(主要终点),PANSS 总分的变化无显著差异(帕利哌酮 ER 组与阿立哌唑组,-19.3[13.80]与-19.8[14.56],p=0.935);应答者比例分别为 67.9%和 76.3%,p=0.119)和第 182 天(-25.6[16.88]与-26.8[18.82],p=0.877;应答者比例分别为 76.8%和 81.6%,p=0.444)。两组的所有次要终点(临床稳定的维持、PANSS 阴性症状的变化、临床总体印象严重程度和个人和社会表现评分)均相似。帕利哌酮 ER 最常见(>10%患者)的治疗相关不良事件为静坐不能、头痛、嗜睡、震颤和体重增加,阿立哌唑为精神分裂症恶化和嗜睡。帕利哌酮 ER 组与阿立哌唑组均有>2%的患者出现锥体外系症状,包括肌张力障碍和运动障碍。

结论

帕利哌酮 ER 在治疗青少年精神分裂症方面并未显示出优于阿立哌唑的疗效。两种药物在症状和功能测量方面均表现出明显的临床改善,且总体耐受性良好。

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