Samalin L, Honciuc M, Llorca P-M
Encephale. 2015 Dec;41(6):541-9. doi: 10.1016/j.encep.2015.09.005.
Lurasidone is a new second-generation antipsychotic approved in March 2014 by the European Medicines Agency for the treatment of schizophrenia. Lurasidone has demonstrated its efficacy in long-term studies. It has been shown to reduce significantly the risk of relapse in comparison with placebo in patients with schizophrenia. In comparator study, lurasidone was noninferior to quetiapine XR in risk for relapse. In open-label studies, lurasidone was associated with sustained improvement in efficacy measures observed and well-tolerated inpatients with schizophrenia who had switched to lurasidone from another antipsychotic. Available evidence showed also that lurasidone might be involved in the long-term improvement of cognitive performance in schizophrenic patients. Lurasidone differs from the other second-generation antipsychotics by a good tolerability profile, in particular in terms of metabolic and cardiovascular profiles. Lurasidone seems to have a moderate link with the occurrence of akathisia and extrapyramidal symptoms. Although lurasidone long-acting formulation is lacking, the long-term profile of lurasidone appears compatible with a good acceptability and consequently a good compliance to treatment of patients with schizophrenia.
鲁拉西酮是一种新型第二代抗精神病药物,于2014年3月获欧洲药品管理局批准用于治疗精神分裂症。鲁拉西酮在长期研究中已证明其疗效。与精神分裂症患者使用安慰剂相比,它已显示出能显著降低复发风险。在对照研究中,鲁拉西酮在复发风险方面不劣于喹硫平缓释片。在开放标签研究中,对于从其他抗精神病药物换用鲁拉西酮的精神分裂症患者,鲁拉西酮与观察到的疗效持续改善相关,且耐受性良好。现有证据还表明,鲁拉西酮可能有助于精神分裂症患者认知功能的长期改善。鲁拉西酮与其他第二代抗精神病药物不同,具有良好的耐受性,尤其是在代谢和心血管方面。鲁拉西酮似乎与静坐不能和锥体外系症状的发生有中度关联。尽管鲁拉西酮缺乏长效制剂,但其长期表现似乎具有良好的可接受性,从而使精神分裂症患者对治疗有良好的依从性。