Safety and effectiveness of fingolimod in Japanese patients with multiple sclerosis: Results of a post-marketing surveillance study

Q4 Immunology and Microbiology
Noriko Sato, Koji Wakimoto, Kyoko Kato, Yutaka Susuta, Kengo Ueda, Yoshihisa Satou, Takayoshi Sasajima, Jun-ichi Kira
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引用次数: 0

Abstract

Objective

Fingolimod is the first oral sphingosine-1-phosphate receptor modulator approved in Japan for multiple sclerosis (MS). A large Japanese observational study of fingolimod in patients with MS was carried out to support its safety and effectiveness in a real-world setting.

Methods

This 2-year, prospective, multicenter, single-cohort, observational study included all Japanese patients with MS who initiated fingolimod (0.5 mg/day). Safety endpoints included adverse events and adverse drug reactions. Effectiveness endpoints included the annualized relapse rate, Kurtzke's Expanded Disability Status Scale score and physician clinical global impression. All endpoints were analyzed in fingolimod-naïve patients.

Results

Of the 1792 patients who started fingolimod between 28 November 2011 and 31 May 2013, 1624 and 1623 fingolimod-naïve patients were included in the safety and effectiveness analysis sets, respectively. The most common MS type was relapsing–remitting MS (89.47%). Adverse events, adverse events leading to discontinuation of fingolimod, adverse drug reactions and serious adverse drug reaction incidences were 64.10%, 15.33%, 57.88% and 23.46%, respectively. No new/unexpected safety signals were identified. The annualized relapse rate was 0.97 during the 1 year before baseline, and decreased to 0.22 after treatment. The mean Expanded Disability Status Scale score remained stable throughout treatment, irrespective of the baseline Expanded Disability Status Scale score (≥3 or <3). Physician clinical global impression was classified as ‘effective’ in the majority of patients (70.3%–90.1%) throughout the treatment period.

Conclusion

Fingolimod was well tolerated and no new safety concerns were identified in this Japanese 2-year post-marketing study. Additionally, fingolimod was effective in preventing MS relapse and physical disability progression in this real-world population comprising mainly relapsing–remitting MS patients.

Abstract Image

芬戈莫德在日本多发性硬化症患者中的安全性和有效性:上市后监测研究的结果
芬戈莫德是首个在日本获批用于多发性硬化症(MS)的口服鞘氨醇-1-磷酸受体调节剂。日本开展了一项大型观察性研究,对芬戈莫德在MS患者中的应用进行了研究,以支持其在现实世界中的安全性和有效性。方法:这项为期2年、前瞻性、多中心、单队列、观察性研究纳入了所有接受芬戈莫(0.5 mg/d)治疗的日本MS患者。安全终点包括不良事件和药物不良反应。疗效终点包括年复发率、Kurtzke's扩展残疾状态量表评分和医生临床总体印象。对fingolimod-naïve患者的所有终点进行分析。结果在2011年11月28日至2013年5月31日期间开始使用芬戈莫德的1792例患者中,分别有1624例和1623例fingolimod-naïve患者被纳入安全性和有效性分析集。最常见的MS类型为复发缓解型MS(89.47%)。不良事件发生率为64.10%,不良事件发生率为15.33%,药物不良反应发生率为57.88%,严重不良反应发生率为23.46%。没有发现新的/意外的安全信号。基线前1年的年化复发率为0.97,治疗后降至0.22。在整个治疗过程中,无论基线扩展残疾状态量表评分(≥3或<;3)如何,扩展残疾状态量表的平均得分保持稳定。在整个治疗期间,大多数患者(70.3%-90.1%)的医生临床总体印象被归类为“有效”。结论:在日本进行的为期2年的上市后研究中,Fingolimod耐受性良好,未发现新的安全性问题。此外,在主要由复发缓解型MS患者组成的现实人群中,fingolimod可有效预防MS复发和身体残疾进展。
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来源期刊
Clinical and Experimental Neuroimmunology
Clinical and Experimental Neuroimmunology Immunology and Microbiology-Immunology and Microbiology (miscellaneous)
CiteScore
1.60
自引率
0.00%
发文量
52
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