Weinblatt M E, Kaplan H, Germain B F, Merriman R C, Solomon S D, Wall B, Anderson L, Block S, Small R, Wolfe F
Department of Rheumatology and Immunology, Brigham and Women's Hospital, Boston, MA 02115.
J Rheumatol. 1991 Mar;18(3):334-8.
One hundred and twenty-three patients with rheumatoid arthritis (RA) who successfully completed a randomized trial comparing oral methotrexate (MTX) to auranofin enrolled in a longterm prospective study of oral MTX. Of the 91 patients who completed 24 months of therapy, a significant (p = 0.0001) improvement was noted compared to baseline in all clinical disease variables and the Westergren erythrocyte sedimentation rate (ESR). Marked improvement occurred in 94 (76%) and 98 (80%) of the patients in the joint pain/tenderness index and joint swelling index at the last evaluable visit (mean 26 months). Of the 77 patients with an elevated ESR at baseline, 29 (38%) patients normalized it (less than 20 mm/h) while receiving therapy (p less than 0.01). A significant reduction in prednisone dose was also seen. Adverse events occurred frequently but were generally mild in severity. Twenty-seven patients (22%) withdrew during the study. Four (3%) withdrew due to lack of efficacy, and 6 (5%) because of adverse experiences. The overall probability of continuing therapy in the study for 48 months was projected at 72%. This large prospective study supports the observation of earlier smaller studies that MTX is an effective drug in the treatment of RA.
123例类风湿关节炎(RA)患者成功完成了一项比较口服甲氨蝶呤(MTX)与金诺芬的随机试验,随后参加了一项口服MTX的长期前瞻性研究。在完成24个月治疗的91例患者中,所有临床疾病变量和魏氏血沉率(ESR)与基线相比均有显著改善(p = 0.0001)。在最后一次可评估访视时(平均26个月),94例(76%)和98例(80%)患者的关节疼痛/压痛指数和关节肿胀指数有明显改善。在基线时ESR升高的77例患者中,29例(38%)患者在接受治疗期间ESR恢复正常(低于20 mm/h)(p < 0.01)。泼尼松剂量也有显著减少。不良事件频繁发生,但严重程度一般较轻。27例(22%)患者在研究期间退出。4例(3%)因缺乏疗效退出,6例(5%)因不良事件退出。预计该研究中持续治疗48个月的总体概率为72%。这项大型前瞻性研究支持了早期较小规模研究的观察结果,即MTX是治疗RA的有效药物。