Sajatovic Martha, Doring Monica, Lopena Oliver J, Johnston Karen, Turkoz Ibrahim, Josiah Nia, Obando Camilo
University Hospitals Cleveland Medical Center, Case Western Reserve University School of Medicine, Cleveland, OH, USA.
Janssen Scientific Affairs, LLC, a Johnson & Johnson company, Titusville, NJ, USA.
Neuropsychiatr Dis Treat. 2024 Nov 21;20:2227-2235. doi: 10.2147/NDT.S427227. eCollection 2024.
A previous integrated patient-level analysis demonstrated a significant benefit of implementing once-monthly injectable paliperidone palmitate (PP1M) earlier in the treatment course for schizophrenia. Earlier therapeutic interventions during the first 3-5 years after disease onset can positively impact long-term outcomes in schizophrenia. This present analysis evaluated the risk of relapse both overall and by different durations of illness (0-3 years, >3-5 years, and >5 years from diagnosis) in adult patients with schizophrenia who received PP1M or oral antipsychotics (OAPs).
This analysis included integrated patient-level data from the Paliperidone Palmitate Research in Demonstrating Effectiveness (PRIDE) and Prevention of Relapse with Oral Antipsychotics versus Injectable Paliperidone Palmitate (PROSIPAL) studies. Both studies assessed relapse as the primary outcome in patients treated either PP1M or OAPs.
Overall, the risk of relapse was reduced by 31% with PP1M compared to OAP (HR 0.69; 95% CI [0.56-0.86], < 0.001). Fewer relapses were observed with PP1M versus OAP in the 0-3-year subgroup (15.8% and 21.7%, respectively), >3-5-year subgroup (19.6% and 29.9%, respectively), and >5-year subgroup (41.7% and 51.6%, respectively). These results represent a reduction in risk of relapse by 33% for patients receiving PP1M versus OAP in the 0-3-year subgroup (HR 0.67; 95% CI [0.44-1.00], = 0.050), 43% in the >3-5-year subgroup (HR 0.57; 95% CI [0.35-0.93], = 0.025), and 26% in the >5-year subgroup (HR 0.74; 95% CI [0.55-1.00], = 0.049). Treatment-emergent adverse event rates were similar between treatment groups.
This analysis indicates that PP1M provides significant benefits in reducing relapse rates compared to OAPs, regardless of the duration of illness. These findings emphasize the importance of initiating PP1M treatment early in the course of schizophrenia to achieve better long-term outcomes.
之前一项综合患者层面的分析表明,在精神分裂症治疗过程中更早使用每月一次注射用棕榈酸帕利哌酮(PP1M)具有显著益处。疾病发作后的前3至5年进行早期治疗干预可对精神分裂症的长期预后产生积极影响。本分析评估了接受PP1M或口服抗精神病药物(OAPs)的成年精神分裂症患者总体复发风险以及不同病程(诊断后0至3年、>3至5年和>5年)的复发风险。
本分析纳入了棕榈酸帕利哌酮有效性研究(PRIDE)和口服抗精神病药物与注射用棕榈酸帕利哌酮预防复发研究(PROSIPAL)的综合患者层面数据。两项研究均将复发作为接受PP1M或OAPs治疗患者的主要结局指标。
总体而言,与OAPs相比,PP1M使复发风险降低了31%(风险比[HR] 0.69;95%置信区间[CI] [0.56 - 0.86],P < 0.001)。在0至3年亚组(分别为15.8%和21.7%)、>3至5年亚组(分别为19.6%和29.9%)以及>5年亚组(分别为41.7%和51.6%)中,观察到接受PP1M治疗的患者复发次数少于接受OAPs治疗的患者。这些结果表明,在0至3年亚组中,接受PP1M治疗的患者与接受OAPs治疗的患者相比,复发风险降低了33%(HR 0.67;95% CI [0.44 - 1.00],P = 0.050),在>3至5年亚组中降低了43%(HR 0.57;95% CI [0.35 - 0.93],P = 0.025),在>5年亚组中降低了26%(HR 0.74;95% CI [0.55 - 1.00],P = 0.049)。各治疗组治疗中出现的不良事件发生率相似。
本分析表明,与OAPs相比,PP1M在降低复发率方面具有显著益处,无论病程长短如何。这些发现强调了在精神分裂症病程早期启动PP1M治疗以实现更好长期预后的重要性。