Cattaneo Carlo, Sardina Marco, Bonizzoni Ermino
Department of Medical, Zambon SpA, Bresso, Italy.
Department of R &D, Zambon SpA, Bresso, Italy.
J Parkinsons Dis. 2016;6(1):165-73. doi: 10.3233/JPD-150700.
Studies 016 and SETTLE showed that safinamide was safe and effective as adjunct therapy in patients with advanced Parkinson's disease (PD) and motor fluctuations. The addition of safinamide to a stable dose of levodopa alone or with other antiparkinsonian medications significantly increased ON time with no/non-troublesome dyskinesia, decreased OFF time and improved Parkinson's symptoms.
To evaluate the clinical effects of safinamide 100 mg/day on motor fluctuations and cardinal Parkinson's symptoms in specific patient subgroups using pooled data from Studies 016 and SETTLE.
Both studies were double blind, placebo-controlled, randomized, phase 3 trials which enrolled patients with mid- to late-stage PD experiencing motor fluctuations while receiving optimized and stable doses of levodopa, alone or with other dopaminergic treatments. The present post-hoc analyses assessed the change from baseline in ON time (with no or non-troublesome dyskinesia) and OFF time in subgroups of patients who were receiving only levodopa at baseline, who were classified as "mild fluctuators" (daily OFF time ≤4 h), and who were receiving concomitant dopaminergic therapy, with or without amantadine, and the effects of safinamide versus placebo on individual cardinal PD symptoms during ON time.
Safinamide significantly increased mean ON time (with no or non-troublesome dyskinesia) and reduced mean OFF time when used as first adjunct therapy in levodopa-treated patients and patients with mild motor fluctuations. Mean daily ON time (with no or non-troublesome dyskinesia) and OFF time were favorably changed, compared with placebo, to similar extents regardless of whether patients were receiving concomitant dopamine agonists, catechol-O-methyltransferase inhibitors and amantadine. Additionally, safinamide improved bradykinesia, rigidity, tremor and gait.
Safinamide was a safe and effective first adjunct therapy in levodopa-treated patients and improved 4/5 cardinal symptoms of PD while providing benefits to mild and non-mild fluctuators and patients receiving other concomitant dopaminergic therapies.
研究016和SETTLE表明,沙芬酰胺作为辅助治疗药物,用于晚期帕金森病(PD)伴运动波动的患者时安全有效。在稳定剂量的左旋多巴基础上单独添加沙芬酰胺,或与其他抗帕金森药物联用,可显著增加“开”期时间,且无/无严重异动症,减少“关”期时间,并改善帕金森症状。
利用研究016和SETTLE的汇总数据,评估每日100 mg沙芬酰胺对特定患者亚组运动波动和主要帕金森症状的临床效果。
这两项研究均为双盲、安慰剂对照、随机3期试验,纳入中晚期PD且在接受优化稳定剂量左旋多巴单独治疗或联合其他多巴胺能治疗时出现运动波动的患者。本次事后分析评估了基线时仅接受左旋多巴治疗、被分类为“轻度波动者”(每日“关”期时间≤4小时)、正在接受多巴胺能联合治疗(有或无金刚烷胺)的患者亚组中,“开”期时间(无或无严重异动症)和“关”期时间相对于基线的变化,以及沙芬酰胺与安慰剂对“开”期时各个主要PD症状的影响。
在左旋多巴治疗的患者和轻度运动波动的患者中,沙芬酰胺作为首个辅助治疗药物使用时,显著增加了平均“开”期时间(无或无严重异动症),并减少了平均“关”期时间。无论患者是否同时接受多巴胺激动剂、儿茶酚-O-甲基转移酶抑制剂和金刚烷胺治疗,与安慰剂相比,平均每日“开”期时间(无或无严重异动症)和“关”期时间均在相似程度上得到了有利改变。此外,沙芬酰胺改善了运动迟缓、僵硬、震颤和步态。
沙芬酰胺在左旋多巴治疗的患者中是一种安全有效的首个辅助治疗药物,改善了PD的4/5项主要症状,同时对轻度和非轻度波动者以及接受其他多巴胺能联合治疗的患者有益。