Jacob G, Messina M, Kennedy J, Epstein C, Sanda M, Mullane J
J Clin Pharmacol. 1986 Mar;26(3):195-202. doi: 10.1002/j.1552-4604.1986.tb02933.x.
Etodolac was compared with aspirin and placebo for efficacy and safety, and a minimum effective dose was established in 264 patients with adult-onset, active rheumatoid arthritis. In this six-week, 14-center, double-blind, parallel-group investigation, preceded by a washout period of up to two weeks, patients received daily doses of etodolac at 50, 100, or 200 mg/d; aspirin at 3,900 mg/d; or placebo. Both etodolac at the highest dose and aspirin produced statistically significant improvement from baseline in all disease activity assessments measured at four- and six-week end points and were superior to placebo in the majority of assessments. A greater number of patient complaints occurred with aspirin, especially in regard to gastrointestinal-related and otologic side effects. A significant therapeutic dose response was evident among the etodolac groups without an increase in side effects. Although the 100-mg/d dose was effective in many of the efficacy parameters measured, the 200-mg/d dose, which is comparably efficacious to aspirin 3.9 g/d, was suggested as the minimum effective dose for the relief of the signs and symptoms of active rheumatoid arthritis.
将依托度酸与阿司匹林及安慰剂进行了疗效和安全性比较,并在264例成年发病的活动性类风湿性关节炎患者中确定了最低有效剂量。在这项为期六周、涉及14个中心的双盲平行组研究中,先有长达两周的洗脱期,患者每日接受50、100或200mg/d的依托度酸剂量;3900mg/d的阿司匹林剂量;或安慰剂。在四周和六周终点测量的所有疾病活动评估中,最高剂量的依托度酸和阿司匹林与基线相比均产生了统计学上显著的改善,并且在大多数评估中均优于安慰剂。阿司匹林引发的患者投诉更多,尤其是在胃肠道相关和耳科副作用方面。依托度酸组之间存在明显的治疗剂量反应,且副作用未增加。尽管100mg/d剂量在许多测量的疗效参数中有效,但建议200mg/d剂量作为缓解活动性类风湿性关节炎体征和症状的最低有效剂量,该剂量与3.9g/d阿司匹林的疗效相当。