Department of Dermatology, University of Münster, Münster, Germany.
J Am Acad Dermatol. 2011 Dec;65(6):e195-213. doi: 10.1016/j.jaad.2010.06.017. Epub 2010 Aug 30.
In the first part of the review, topical agents and first-line systemic treatment options for cutaneous lupus erythematosus were discussed whereas in the second part, recent information on efficacy, dosage, and side effects for further systemic treatment options are described in detail. In contrast to other immunosuppressive agents, such as azathioprine, cyclophosphamide, and cyclosporine, methotrexate has recently received more attention in the treatment of the disease. Further second-line treatment includes retinoids, dapsone, and mycophenolate mofetil. Because of severe side effects or high costs, other agents, such as thalidomide or high-dose intravenous immunoglobulins, are reserved for severe recalcitrant CLE. Biologics, ie, rituximab, have been used to treat systemic lupus erythematosus; however, in CLE, most biologics have only been applied in single cases. In addition to successful treatment, induction of CLE subtypes by biologics has been reported. In conclusion, many treatment options exist for CLE, but not many are supported by evidence from randomized controlled trials.
在这篇综述的第一部分,我们讨论了治疗红斑狼疮的局部药物和一线全身治疗选择;在第二部分,我们详细描述了其他全身治疗选择的最新疗效、剂量和副作用信息。与其他免疫抑制剂(如硫唑嘌呤、环磷酰胺和环孢素)不同,甲氨蝶呤最近在该疾病的治疗中受到了更多关注。进一步的二线治疗包括类视黄醇、达普司酮和霉酚酸酯。由于严重的副作用或高昂的成本,其他药物(如沙利度胺或大剂量静脉注射免疫球蛋白)仅保留用于严重难治性 CLE。生物制剂,如利妥昔单抗,已被用于治疗系统性红斑狼疮;然而,在 CLE 中,大多数生物制剂仅在单个病例中应用。除了成功治疗外,生物制剂还会诱导 CLE 亚型的出现。总之,有许多治疗选择可用于 CLE,但其中只有少数得到随机对照试验的证据支持。