Jacobs L, Salazar A M, Herndon R, Reese P A, Freeman A, Josefowicz R, Cuetter A, Husain F, Smith W A, Ekes R
Lancet. 1986;2(8521-22):1411-3. doi: 10.1016/s0140-6736(86)92730-3.
In this randomised, double-blind, placebo-controlled, 2-year multicentre study intrathecally administered natural human fibroblast interferon (IFN-B) was effective in reducing exacerbations of multiple sclerosis (MS) in patients with exacerbating/remitting disease. The mean reduction in exacerbation rate of 34 patients who received IFN-B (recipients) was significantly greater during the study than that of 35 patients who received placebo (p less than 0.04). The prestudy exacerbation rates were comparable in recipients and controls, but the rate at the end of the study was significantly lower in recipients than in controls (p less than 0.001). IFN-B was given by nine or ten lumbar punctures over the first 6 months of the study, and patient observations continued for 2 years. IFN-B was well tolerated in 95% of the recipients, and the side-effects experienced were clearly acceptable for the benefits achieved. Low doses of indomethacin reduced the toxicity of IFN-B and played an important role in successful double-blinding.
在这项随机、双盲、安慰剂对照的2年多中心研究中,鞘内注射天然人成纤维细胞干扰素(IFN - B)对缓解期/复发型多发性硬化症(MS)患者减少病情加重有效。接受IFN - B的34例患者(接受者)的病情加重率平均降低幅度在研究期间显著大于接受安慰剂的35例患者(p小于0.04)。接受者和对照组在研究前的病情加重率相当,但研究结束时接受者的病情加重率显著低于对照组(p小于0.001)。在研究的前6个月通过9次或10次腰椎穿刺给予IFN - B,对患者的观察持续2年。95%的接受者对IFN - B耐受性良好,所经历的副作用对于所取得的益处而言明显是可接受的。低剂量的吲哚美辛降低了IFN - B的毒性,并在成功进行双盲研究中发挥了重要作用。