DE Oliveira Juliana Pedroso, Levy Annabelle, Morel Patrice, Guibal Fabien
Department of Dermatology, Saint-Louis Hospital, Paris, France.
J Dermatol. 2008 Sep;35(9):575-80. doi: 10.1111/j.1346-8138.2008.00525.x.
Infliximab treatment has been shown to be effective for moderate-to-severe psoriasis in several large clinical trials. Nonetheless, experience with this new treatment is still needed to evaluate its efficacy and tolerance in everyday practice. In this follow-up study, we report our experience with infliximab for recalcitrant psoriasis. Nineteen patients with recalcitrant psoriasis were treated between July 2004 and December 2006 with 5 mg/kg infliximab i.v. at weeks 0, 2 and 6 followed by maintenance every 8 weeks. In three patients resistant to treatment, methotrexate was added at a 15-25 mg dose weekly after the sixth week of infliximab therapy. Pretreatment evaluations included chest X-ray, tuberculin test (5 units), full blood count, kidney and liver function tests, antinuclear antibodies and patient weight. Response to treatment, using the Psoriasis Area and Severity Index (PASI) score, and adverse effects were prospectively assessed at weeks 0, 6 and 22. At week 6, after only two infusions, 78.9% (15/19) of patients showed at least 75% improvement in baseline PASI (PASI 75). At week 22, 73.6% (14/19) patients had reached PASI 75. Three patients had a relapse. Four developed adverse effects that required suspension of infliximab therapy. No tuberculosis or lymphoproliferative disease was observed. Four patients (21%) showed apparition of positive antinuclear antibody during the course of treatment and 57.8% (11/19) of patients showed an increase in weight at week 22. Our experience shows that infliximab is a very rapidly effective treatment of severe, treatment-resistant psoriasis as soon as the sixth week of treatment.
在多项大型临床试验中,英夫利昔单抗治疗已被证明对中重度银屑病有效。尽管如此,仍需要积累这种新疗法在日常实践中的经验,以评估其疗效和耐受性。在这项随访研究中,我们报告了使用英夫利昔单抗治疗顽固性银屑病的经验。2004年7月至2006年12月期间,19例顽固性银屑病患者接受了静脉注射英夫利昔单抗治疗,剂量为5mg/kg,分别在第0、2和6周给药,随后每8周维持治疗一次。在3例治疗抵抗的患者中,英夫利昔单抗治疗第6周后,加用了每周15 - 25mg剂量的甲氨蝶呤。治疗前评估包括胸部X线检查、结核菌素试验(5单位)、全血细胞计数、肝肾功能检查、抗核抗体检测及患者体重测定。使用银屑病面积和严重程度指数(PASI)评分对治疗反应及不良反应进行前瞻性评估,评估时间点为第0、6和22周。在第6周,仅经过两次输注后,78.9%(15/19)的患者基线PASI改善至少达75%(PASI 75)。在第22周,73.6%(14/19)的患者达到PASI 75。3例患者复发。4例出现不良反应,需要暂停英夫利昔单抗治疗。未观察到结核病或淋巴增殖性疾病。4例患者(21%)在治疗过程中抗核抗体呈阳性,57.8%(11/19)的患者在第22周体重增加。我们的经验表明,英夫利昔单抗对重度、治疗抵抗性银屑病是一种起效非常迅速的治疗方法,在治疗第6周时即可显现效果。