Relapse Rates With Paliperidone Palmitate in Adult Patients With Schizophrenia: Results for the 6-Month Formulation From an Open-label Extension Study Compared to Real-World Data for the 1-Month and 3-Month Formulations.

IF 4.5 2区 医学 Q1 CLINICAL NEUROLOGY
Ibrahim Turkoz, Mehmet Daskiran, Uzma Siddiqui, R Karl Knight, Karen L Johnston, Christoph U Correll
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引用次数: 0

Abstract

Background: The 3 paliperidone palmitate (PP) long-acting injectable antipsychotic formulations, PP 1-month (PP1M), PP 3-month (PP3M), and PP 6-month (PP6M), have shown to reduce the risk of relapse in schizophrenia. The current phase-4 study constructed external comparator arms (ECAs) using real-world data for PP3M and PP1M and compared relapse prevention rates with PP6M from an open-label extension (OLE) study in adult patients with schizophrenia.

Methods: PP6M data were derived from a single-arm, 24-month, OLE study (NCT04072575), which included patients with schizophrenia who completed a 12-month randomized, double-blind, noninferiority, phase-3 study (NCT03345342) without relapse. Patients in the PP3M and PP1M ECAs were identified from the IBM® MarketScan® Multistate Medicaid Database based on similar eligibility criteria as the PP6M cohort.

Results: A total of 178 patients were included in each cohort following propensity score matching. Most patients were men (>70%; mean age: 39-41 years). Time to relapse (primary analysis based on Kaplan-Meier estimates) was significantly delayed in the PP6M cohort (P < .001, log-rank test). The relapse rate was lower in the PP6M cohort (3.9%) vs PP3M (20.2%) and PP1M (29.8%) cohorts. Risk of relapse decreased significantly (P < .001) by 82% for PP6M vs PP3M (HR = 0.18 [95% CI = 0.08 to 0.40]), 89% for PP6M vs PP1M (HR = 0.11 [0.05 to 0.25]), and 35% for PP3M vs PP1M (HR = 0.65 [0.42 to 0.99]; P = .043). Sensitivity analysis confirmed findings from the primary analysis. Although the ECAs were matched to mimic the characteristics of the PP6M cohort, heterogeneity between the groups could exist due to factors including prior study participation, unmeasured confounders, variations in data capture and quality, and completeness of clinical information.

Conclusions: In a clinical trial setting, PP6M significantly delayed time to relapse and demonstrated lower relapse rates compared with PP3M and PP1M treatments in real-world settings among adult patients with schizophrenia.

Trial registration: ClinicalTrials.gov Identifier: NCT04072575; EudraCT number: 2018-004532-30.

帕潘立酮棕榈酸酯治疗成人精神分裂症患者的复发率:为期 6 个月的开放标签延长期研究结果与为期 1 个月和 3 个月制剂的实际数据对比。
背景:帕利哌酮棕榈酸酯(PP)的三种长效注射抗精神病药物配方,即PP 1个月(PP1M)、PP 3个月(PP3M)和PP 6个月(PP6M),已被证明可降低精神分裂症的复发风险。目前的第四阶段研究利用PP3M和PP1M的真实世界数据构建了外部比较臂(ECA),并将精神分裂症成人患者的复发预防率与开放标签扩展(OLE)研究中的PP6M进行了比较:PP6M的数据来自一项为期24个月的单臂OLE研究(NCT04072575),该研究纳入了完成了为期12个月的随机、双盲(DB)、非劣效、3期研究(NCT03345342)且未复发的精神分裂症患者。PP3M 和 PP1M ECA 中的患者是从 IBM® MarketScan® 多州医疗补助数据库中根据与 PP6M 队列相似的资格标准确定的:经过倾向得分匹配后,每个队列共纳入了 178 名患者。大多数患者为男性(>70%);平均年龄为 39-41 岁。PP6M队列的复发时间(基于Kaplan-Meier估计值的主要分析)明显推迟(PC结论:在临床试验中,PP6M队列的复发时间比PP6M队列明显推迟:在临床试验中,与PP3M和PP1M治疗相比,PP6M可显著延迟精神分裂症成年患者的复发时间,并降低复发率。
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来源期刊
CiteScore
8.40
自引率
2.10%
发文量
230
审稿时长
4-8 weeks
期刊介绍: The central focus of the journal is on research that advances understanding of existing and new neuropsychopharmacological agents including their mode of action and clinical application or provides insights into the biological basis of psychiatric disorders and thereby advances their pharmacological treatment. Such research may derive from the full spectrum of biological and psychological fields of inquiry encompassing classical and novel techniques in neuropsychopharmacology as well as strategies such as neuroimaging, genetics, psychoneuroendocrinology and neuropsychology.
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