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N Engl J Med:异丁司特治疗进行性多发性硬化症喜忧参半

2018-09-28 吴星 环球医学网

美国学者在《N Engl J Med》发表了异丁司特治疗进行性多发性硬化症的2期试验。

美国学者在《N Engl J Med》发表了异丁司特治疗进行性多发性硬化症的2期试验。

背景:进行性多发性硬化症的疗法有限。在进行性多发性硬化症中,异丁司特可抑制一些环化核苷酸磷酸二酯酶、巨噬细胞移动抑制因子和Toll样受体4,还可穿过血脑屏障,具有潜在的有益作用。

方法:研究者在口服异丁司特(≤100mg每天一次)或安慰剂治疗96周的2期随机试验中,纳入了原发性或继发性进行性多发性硬化症患者。首要有效性终点为脑萎缩率,其通过脑实质成分测量(相对于脑外表面轮廓体积的脑大小)。主要次要终点包括弥散张量成像显示的锥体束改变、正常表现的脑组织磁化转移率、视网膜神经纤维层厚度、皮质萎缩,所有都是多发性硬化症中的组织损伤测量指标。

结果:进行随机分组的255名患者中,异丁司特组129人,安慰剂组126人。异丁司特组和安慰剂组分别有总共53%和52%的患者具有原发性进行性疾病;其他患者具有继发性进行性疾病。异丁司特组和安慰剂组脑实质成分改变率分别为-0.0010/年和-0.0019/年(差异,0.0009;95% 置信区间[CI],0.00004~0.0017;P=0.04),代表了96周期间,异丁司特组脑组织的损失减少了约2.5mL。异丁司特的不良事件包括肠道症状、头痛和抑郁。

结论:在进行性多发性硬化症患者的2期试验中,与安慰剂相比,异丁司特与脑萎缩的缓慢进展相关,但与较高的肠道副作用、头痛和抑郁发生率相关。(NN102/SPRINT-MS ClinicalTrials.gov编号,NCT01982942)

原始出处:
Fox RJ, Coffey CS, Conwit R,et al.Phase 2 Trial of Ibudilast in Progressive Multiple Sclerosis.N Engl J Med. 2018 Aug 30;379(9):846-855. doi: 10.1056/NEJMoa1803583.

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    2019-01-14 spoonycyy
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    2019-01-17 haouestc
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    2019-07-26 jml2009
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