Zhang LiLi, Li JiTao, Zhao YanJie, Su Yun'Ai, Si Tianmei
Medical Affairs, Xian Janssen Pharmaceutical Co, Ltd, Beijing, People's Republic of China.
National Clinical Research Center for Mental Disorders, Beijing, People's Republic of China; Peking University Sixth Hospital, Institute of Mental Health, Beijing, People's Republic of China; The Key Laboratory of Mental Health, Ministry of Health, Peking University, Beijing, People's Republic of China.
Neuropsychiatr Dis Treat. 2016 Jan 11;12:113-31. doi: 10.2147/NDT.S64672. eCollection 2016.
Paliperidone (9-hydroxyrisperidone), the major active metabolite of risperidone, has been introduced as a novel atypical antipsychotic agent in many countries. It is available both as an oral extended-release (ER) formulation and as a long-acting injection (paliperidone palmitate, PP), which have been approved for treating schizophrenia in the People's Republic of China since 2009 and 2012, respectively. This systematic review summarizes the efficacy, effectiveness, and safety of paliperidone in the treatment of schizophrenia in the Chinese population.
A systematic literature search was conducted on the databases covering international and Chinese core journals, published from January 1, 2008, to May 22, 2015.
A total of 122 publications were retrieved, of which 63 studies were identified for inclusion; most studies were related to paliperidone ER (n=53), nine were related to PP, and one study was related to both agents. Paliperidone ER demonstrated at least comparable efficacy with active comparators, including risperidone, olanzapine, ziprasidone, or aripiprazole, and was found to be superior with respect to the onset of action and improvement in the Personal and Social Performance Scale score. Paliperidone ER appeared to be associated with a lower risk of metabolic syndromes; the most common treatment-emergent adverse events were extrapyramidal symptoms, akathisia, insomnia, and somnolence. Results from interventional and observational studies showed that PP was also an effective and well-tolerated treatment for Chinese patients with schizophrenia. The findings were generally consistent with those observed in non-Chinese populations.
Both paliperidone ER and PP were effective and well-tolerated agents for the treatment of schizophrenia in the Chinese population according to the data we reviewed. No new safety signals specific for the Chinese population were raised for paliperidone. Further studies may be needed to collect more data on long-term treatment of schizophrenia in the People's Republic of China.
帕利哌酮(9-羟基利培酮)是利培酮的主要活性代谢产物,已在许多国家作为一种新型非典型抗精神病药物推出。它有口服缓释(ER)制剂和长效注射剂(帕利哌酮棕榈酸酯,PP)两种剂型,分别于2009年和2012年在中国被批准用于治疗精神分裂症。本系统评价总结了帕利哌酮在中国人群中治疗精神分裂症的疗效、有效性和安全性。
对2008年1月1日至2015年5月22日发表的涵盖国际和中国核心期刊的数据库进行系统文献检索。
共检索到122篇文献,其中63项研究被确定纳入;大多数研究与帕利哌酮ER有关(n = 53),9项与PP有关,1项研究与两种制剂均有关。帕利哌酮ER显示出至少与活性对照药相当的疗效,这些对照药包括利培酮、奥氮平、齐拉西酮或阿立哌唑,并且在起效时间和个人及社会功能量表评分改善方面被发现更具优势。帕利哌酮ER似乎与代谢综合征风险较低相关;最常见的治疗中出现的不良事件是锥体外系症状、静坐不能、失眠和嗜睡。干预性和观察性研究结果表明,PP对中国精神分裂症患者也是一种有效且耐受性良好的治疗方法。这些发现总体上与在非中国人群中观察到的结果一致。
根据我们所回顾的数据,帕利哌酮ER和PP对中国人群治疗精神分裂症均是有效且耐受性良好的药物。未发现帕利哌酮有针对中国人群的新的安全信号。可能需要进一步研究以收集更多关于在中国长期治疗精神分裂症的数据。