O'Donnell Amy, Rao Sanjai, Turkoz Ibrahim, Gopal Srihari, Kim Edward
Janssen Scientific Affairs, LLC, Titusville, NJ, USA.
Department of Psychiatry, University of California, San Diego, La Jolla, CA, USA.
Neuropsychiatr Dis Treat. 2021 Jan 6;17:1-9. doi: 10.2147/NDT.S278298. eCollection 2021.
Paliperidone palmitate once every 3 months (PP3M) is indicated in adults with schizophrenia adequately treated with once-monthly paliperidone palmitate (PP1M) for at least 4 months, in whom the last two consecutive doses are the same. The decision of when to transition to PP3M is based on the patient's symptom status while receiving PP1M.
In a double-blind relapse-prevention study (NCT01529515), patients who met Positive and Negative Syndrome Scale (PANSS) score stabilization criteria after 4 months of PP1M were eligible for transition to PP3M; those who continued to meet stabilization criteria after 12 weeks following an open-label PP3M dose were randomized to receive PP3M or placebo. We compared (post hoc) PANSS, Clinical Global Impression-Severity (CGI-S), and Personal and Social Performance (PSP) scores during the pre-randomization, open-label phase in patients in randomized versus non-randomized groups using analysis of variance or chi-square tests.
Of 506 patients enrolled, 305 were randomized. After 4 months' PP1M treatment, PANSS and CGI-S scores were significantly lower and PSP scores significantly higher in randomized patients versus non-randomized patients (least squares means [95% CI]: 57.1 [55.7, 58.6] vs 62.2 [60.0, 64.3], 2.9 [2.8, 3.1] vs 3.3 [3.1, 3.4], and 67.0 [65.7, 68.3] vs 64.5 [62.6, 66.4], respectively); changes from baseline between groups differed significantly (all ≤0.009).
Confirming adequate stabilization with PP1M prior to transitioning to PP3M is critical in maximizing treatment response; clinicians should consider transitioning patients to PP3M only if patients respond well to PP1M for at least 4 months and their last two consecutive doses are the same.
对于接受每月一次棕榈酸帕利哌酮(PP1M)充分治疗至少4个月且最后连续两剂相同的精神分裂症成人患者,可每三个月使用一次棕榈酸帕利哌酮(PP3M)进行治疗。何时过渡到PP3M的决定基于患者接受PP1M治疗时的症状状态。
在一项双盲预防复发研究(NCT01529515)中,在接受PP1M治疗4个月后符合阳性和阴性症状量表(PANSS)评分稳定标准的患者有资格过渡到PP3M;在接受开放标签的PP3M剂量12周后仍符合稳定标准的患者被随机分配接受PP3M或安慰剂。我们使用方差分析或卡方检验,比较了随机分组组和非随机分组组患者在随机化前开放标签阶段的PANSS、临床总体印象-严重程度(CGI-S)和个人与社会功能(PSP)评分(事后分析)。
在纳入的506例患者中,305例被随机分组。在接受4个月的PP1M治疗后,随机分组患者的PANSS和CGI-S评分显著低于非随机分组患者,PSP评分显著高于非随机分组患者(最小二乘均值[95%置信区间]:分别为57.1[55.7,58.6]对62.2[60.0,64.3]、2.9[2.8,3.1]对3.3[3.1,3.4]、67.0[65.7,68.3]对64.5[62.6,66.4]);两组间相对于基线的变化差异显著(均≤0.009)。
在过渡到PP3M之前,确认使用PP1M达到充分稳定对于最大化治疗反应至关重要;临床医生应仅在患者对PP1M至少有4个月良好反应且最后连续两剂相同的情况下,才考虑将患者过渡到PP3M。