Sfriso Paolo, Botsios Costantino, Ostuni Pierantonio, Todesco Silvano
Cattedra e Divisione di Reumatologia, Istituto di Medicina Interna, Università, Padova.
Recenti Prog Med. 2002 Jul-Aug;93(7-8):416-20.
Infliximab is a chimeric anti-tumor necrosis factor alpha (anti-TNF-alpha) monoclonal IgG1 antibody successfully used for the treatment of active rheumatoid arthritis (RA) not completely controlled with methotrexate or other disease modifying anti-rheumatic drugs. We evaluated both clinical efficacy and safety of infliximab in 63 patients with persistently active RA (Disease activity score > or = 3.7). All the patients received infliximab (3 mg/Kg) at week 0, 2, 6 and then every 5 weeks in combination with methotrexate (7.5-10 mg/week) in an open label study. At week 14th, ACR 20% response criteria have been fulfilled by 43 (91.4%) out of 47 patients, 31 (72%) of them achieving also an ACR 50% and 9 (21%) an ACR 70% response. At the time of this report 33 patients touched 22 weeks of treatment: ACR 20% response was achieved in 95%, while ACR 50% and ACR 70% were respectively found in 78% and 39% of the cases. Only 1 case of bronchopulmonary mycosis and 2 of mild urticaria were observed. The initiation of infliximab therapy in patients with active RA resulted in a rapid and sustained improvement of articular manifestations and quality of life. Even though, major adverse events were rare, clinicians should be aware of this possibility.
英夫利昔单抗是一种嵌合型抗肿瘤坏死因子α(抗TNF-α)单克隆IgG1抗体,已成功用于治疗甲氨蝶呤或其他改善病情的抗风湿药物未能完全控制的活动性类风湿关节炎(RA)。我们评估了英夫利昔单抗对63例持续性活动性RA(疾病活动评分≥3.7)患者的临床疗效和安全性。在一项开放标签研究中,所有患者在第0、2、6周接受英夫利昔单抗(3mg/kg)治疗,随后每5周一次,并联合甲氨蝶呤(7.5 - 10mg/周)。在第14周时,47例患者中有43例(91.4%)达到美国风湿病学会(ACR)20%反应标准,其中31例(72%)达到ACR 50%反应,9例(21%)达到ACR 70%反应。在本报告发布时,33例患者接受了22周的治疗:95%的患者达到ACR 20%反应,而达到ACR 50%和ACR 70%反应的患者分别为78%和39%。仅观察到1例支气管肺霉菌病和2例轻度荨麻疹。对活动性RA患者开始使用英夫利昔单抗治疗可迅速并持续改善关节表现和生活质量。尽管严重不良事件罕见,但临床医生应意识到这种可能性。