Radue Ernst-Wilhelm, Sprenger Till, Gaetano Laura, Mueller-Lenke Nicole, Cavalier Steve, Thangavelu Karthinathan, Panzara Michael A, Donaldson Jessica E, Woodward Fiona M, Wuerfel Jens, Wolinsky Jerry S, Kappos Ludwig
Medical Image Analysis Center (MIAC AG) (E.-W.R., L.G., N.M.-L., J.W.), Basel, Switzerland; DKD HELIOS Klinik (T.S.), Wiesbaden, Germany; Neurologic Clinic and Policlinic (T.S., L.G., L.K.), University Hospital Basel and University of Basel, Switzerland; Sanofi Genzyme (S.C., K.T.), Previously Sanofi Genzyme (M.A.P.), and WAVE Life Sciences (M.A.P.), Cambridge, MA; Fishawack Communications Ltd (J.E.D., F.M.W.), Abingdon, Oxfordshire, UK; and McGovern Medical School (J.S.W.), UTHealth, Houston, TX.
Neurol Neuroimmunol Neuroinflamm. 2017 Aug 9;4(5):e390. doi: 10.1212/NXI.0000000000000390. eCollection 2017 Sep.
To assess, using structural image evaluation using normalization of atrophy (SIENA), the effect of teriflunomide, a once-daily oral immunomodulator, on brain volume loss (BVL) in patients with relapsing forms of MS enrolled in the phase 3 TEMSO study.
TEMSO MR scans were analyzed (study personnel masked to treatment allocation) using SIENA to assess brain volume changes between baseline and years 1 and 2 in patients treated with placebo or teriflunomide. Treatment group comparisons were made via rank analysis of covariance.
Data from 969 patient MRI visits were included in this analysis: 808 patients had baseline and year 1 MRI; 709 patients had baseline and year 2 MRI. Median percentage BVL from baseline to year 1 and year 2 for placebo was 0.61% and 1.29%, respectively, and for teriflunomide 14 mg, 0.39% and 0.90%, respectively. BVL was lower for teriflunomide 14 mg vs placebo at year 1 (36.9% relative reduction, = 0.0001) and year 2 (30.6% relative reduction, = 0.0001). Teriflunomide 7 mg was also associated with significant reduction in BVL vs placebo over the 2-year study. The significant effects of teriflunomide 14 mg on BVL were observed in both patients with and without on-study disability worsening.
The significant reduction of BVL vs placebo over 2 years achieved with teriflunomide is consistent with its effects on delaying disability worsening and suggests a neuroprotective potential.
Class II evidence shows that teriflunomide treatment significantly reduces BVL over 2 years vs placebo.
NCT00134563.
采用脑萎缩标准化结构图像评估(SIENA),评估每日一次口服免疫调节剂特立氟胺对纳入3期TEMSO研究的复发型多发性硬化症(MS)患者脑容量丢失(BVL)的影响。
使用SIENA分析TEMSO磁共振成像扫描(研究人员对治疗分配情况不知情),以评估接受安慰剂或特立氟胺治疗的患者在基线、第1年和第2年之间的脑容量变化。通过协方差秩分析进行治疗组比较。
本分析纳入了969例患者的MRI检查数据:808例患者有基线和第1年的MRI检查;709例患者有基线和第2年的MRI检查。安慰剂组从基线到第1年和第2年的BVL中位数百分比分别为0.61%和1.29%,特立氟胺14 mg组分别为0.39%和0.90%。在第1年(相对降低36.9%,P = 0.0001)和第2年(相对降低30.6%,P = 0.0001),特立氟胺14 mg组的BVL低于安慰剂组。在为期2年的研究中,特立氟胺7 mg组与安慰剂组相比,BVL也显著降低。在有和没有研究期间残疾恶化的患者中均观察到特立氟胺14 mg对BVL的显著影响。
特立氟胺与安慰剂相比,在2年内显著降低BVL,这与其延缓残疾恶化的作用一致,并提示其具有神经保护潜力。
II类证据表明,与安慰剂相比,特立氟胺治疗在2年内可显著降低BVL。
NCT00134563。