Meyer Jonathan M, Simmons Adam, Jiang Ying, Graham Christine, Yagoda Sergey, McDonnell David
University of California San Diego School of Medicine, La Jolla, CA, USA.
Alkermes, Inc., Waltham, MA, USA.
CNS Spectr. 2023 Aug;28(4):478-481. doi: 10.1017/S1092852922000967. Epub 2022 Oct 13.
A combination of olanzapine and the opioid receptor antagonist samidorphan (OLZ/SAM) has been approved in the United States for the treatment of adults with schizophrenia or adults with bipolar I disorder. In a phase 3 study in adults with schizophrenia (ENLIGHTEN-2), OLZ/SAM treatment was associated with significantly less weight gain compared with olanzapine. Prespecified subgroup analyses explored the consistency of the weight mitigation effect of OLZ/SAM vs olanzapine across demographic subgroups in ENLIGHTEN-2.
The multicenter, randomized, double-blind ENLIGHTEN-2 study (NCT02694328) included outpatients aged 18-55 years with a diagnosis of schizophrenia based on DSM-5 criteria, a body mass index (BMI) of 18 to 30 kg/m, and stable body weight (self-reported change ≤5% for ≥3 months before study entry). Patients were randomized 1:1 to receive OLZ/SAM or olanzapine for 24 weeks. Co-primary endpoints (previously reported) were percent change in body weight and proportion of patients with at least 10% weight gain from baseline at week 24. Prespecified exploratory subgroup analyses by sex, age, self-reported race, and baseline BMI were conducted.
At week 24, treatment with OLZ/SAM resulted in numerically less percent weight gain than with olanzapine across all subgroups evaluated. The proportion of patients with at least 10% weight gain was smaller in each subgroup treated with OLZ/SAM vs olanzapine.
In these exploratory subgroup analyses from the ENLIGHTEN-2 study, weight-mitigating effects of OLZ/SAM vs olanzapine were observed consistently across patient subgroups and were in line with results from the overall study population.
奥氮平与阿片受体拮抗剂塞美多芬(OLZ/SAM)联合用药已在美国获批用于治疗成人精神分裂症或成人双相I型障碍。在一项针对成人精神分裂症患者的3期研究(ENLIGHTEN-2)中,与奥氮平相比,OLZ/SAM治疗导致的体重增加显著更少。预先设定的亚组分析探讨了在ENLIGHTEN-2研究中,OLZ/SAM与奥氮平相比减轻体重效果在不同人口统计学亚组中的一致性。
多中心、随机、双盲的ENLIGHTEN-2研究(NCT02694328)纳入了年龄在18至55岁、根据《精神疾病诊断与统计手册》第5版标准诊断为精神分裂症、体重指数(BMI)为18至30kg/m²且体重稳定(研究入组前≥3个月自我报告体重变化≤5%)的门诊患者。患者按1:1随机分组,接受OLZ/SAM或奥氮平治疗24周。共同主要终点(先前已报告)为体重变化百分比以及在第24周时体重较基线至少增加10%的患者比例。进行了按性别、年龄、自我报告种族和基线BMI的预先设定探索性亚组分析。
在第24周时,在所有评估的亚组中,OLZ/SAM治疗导致的体重增加百分比在数值上均低于奥氮平。与奥氮平相比,接受OLZ/SAM治疗的每个亚组中体重至少增加10%的患者比例更小。
在ENLIGHTEN-2研究的这些探索性亚组分析中,在各患者亚组中均一致观察到OLZ/SAM与奥氮平相比具有减轻体重的效果,且与总体研究人群的结果一致。