Yoshitani Hiroshi, Ito Junko, Kozono Hideki
Pharmaceutical & Medical Device Vigilance Department, Toray Industries, Inc., Tokyo, Japan.
Hepat Med. 2022 May 2;14:37-66. doi: 10.2147/HMER.S352775. eCollection 2022.
Nalfurafine (Remitch, Toray Industries, Inc.) is a selective κ-receptor agonist approved in Japan for the improvement of pruritus in patients with chronic liver diseases (only when existing treatments bring insufficient efficacy) in May 2015.
A post-marketing Specific Drug Use Survey was conducted in Japan (March 1, 2016 to June 30, 2020) of the safety and efficacy of nalfurafine for the improvement of pruritus in patients with chronic liver disease.
Among 1186 cases analyzed for safety, the incidence of adverse drug reactions was 9.4% (112/1186 cases), lower than 61.4% reported in pre-marketing surveillance (297/484 cases). No specific safety issues were found and no cases of concern for drug dependence identified. Efficacy (itch improvement) was demonstrated in 73.16% (815/1114 cases; 12-week analysis set) and in 85.67% (520/607; general assessment of itch improvement at 1-year analysis set). A significant difference was found in 4 items of itch improvement at 12 weeks and 8 items of itch improvement at 1 year. No noteworthy issues were identified. Mean Visual Analog Scale (VAS) values after 12 weeks and 1 year after the first dose were significantly lower than the baseline (p < 0.0001 for both treatment durations). Mean severity scores (Kawashima's classification scheme) were significantly lower than the pretreatment score at 12 weeks and 1 year after the first dose (both p < 0.0001). No concerns were identified in the efficacy and safety of nalfurafine in patients with specific background, ie, the elderly (aged ≥ 65 years), those with renal impairment, and those on long-term treatment (≥ 365 days) compared with patients without corresponding background.
No new safety issues of concern or cases of insufficient efficacy were identified in this Specific Drug Use Survey of the safety and efficacy of nalfurafine for the improvement of pruritus in patients with chronic liver diseases.
纳曲酮(Remitch,东丽工业株式会社)是一种选择性κ受体激动剂,于2015年5月在日本获批用于改善慢性肝病患者的瘙痒(仅在现有治疗效果不佳时使用)。
在日本进行了一项上市后特定药物使用调查(2016年3月1日至2020年6月30日),以评估纳曲酮改善慢性肝病患者瘙痒的安全性和有效性。
在1186例安全性分析病例中,药物不良反应发生率为9.4%(112/1186例),低于上市前监测报告的61.4%(297/484例)。未发现特定的安全问题,也未发现令人担忧的病例。在73.16%(815/1114例;12周分析集)和85.67%(520/607例;1年分析集的瘙痒改善总体评估)的病例中显示出疗效(瘙痒改善)。在12周时的4项瘙痒改善指标和1年时的8项瘙痒改善指标中发现了显著差异。未发现值得注意的问题。首次给药后12周和1年的平均视觉模拟量表(VAS)值显著低于基线(两个治疗期均p < 0.0001)。平均严重程度评分(川岛分类法)在首次给药后12周和1年时显著低于治疗前评分(均p < 0.0001)。与无相应背景的患者相比,纳曲酮在特定背景患者(即老年人(年龄≥65岁)、肾功能不全患者和长期治疗(≥365天)患者)中的疗效和安全性未发现问题。
在这项关于纳曲酮改善慢性肝病患者瘙痒的安全性和有效性的特定药物使用调查中,未发现新的令人担忧的安全问题或疗效不足的病例。