Kuitwaard Krista, van Doorn Pieter A
Department of Neurology, Erasmus MC, s-Gravendijkwal 230, Rotterdam, the Netherlands.
Drugs. 2009 May 29;69(8):987-1001. doi: 10.2165/00003495-200969080-00004.
Chronic inflammatory demyelinating polyradiculoneuropathy (CIDP) is an immune-mediated disorder with variable symptoms and severity that can be difficult to diagnose. Intravenous immunoglobulin, plasma exchange and corticosteroids have all been proven to be beneficial in randomized controlled trials, although the proof for corticosteroids is less clear. Although these treatments are likely to be similar in efficacy, they differ in terms of their cost, availability and adverse effects. These characteristics should be taken into account when deciding which treatment to offer a patient. If there is no response to the first treatment option, one of the other treatments should be tried. Patients with a pure motor CIDP may deteriorate after corticosteroid treatment. Some patients do not respond or become refractory or intolerant to these conventional treatments. Those who become unresponsive to therapy should be checked again for the appearance of a monoclonal protein or other signs of malignancy. Over the years, small non-randomized studies have reported possible beneficial effects of various immunosuppressive agents. A Cochrane review concluded that currently there is insufficient evidence to decide whether these immunosuppressive drugs are beneficial in CIDP. When giving immunosuppressive drugs, one should be aware that some might even cause demyelinating disease. It is difficult to prove beneficial effects of these newer treatments since they have only been used in small groups of patients, who are refractory to other treatments, and often in combination with other treatments. CIDP patients can deteriorate during or after infections or improve spontaneously, making it more difficult to judge treatment efficacy. Various treatments for CIDP are described such as azathioprine, ciclosporin, cyclophosphamide, interferons, methotrexate, mycophenolate mofetil, rituximab and etanercept. An overview of these newer treatments, their mode of action, adverse effects and potential place in the spectrum of treatments for CIDP based on previous reports and their level of evidence is given.
慢性炎症性脱髓鞘性多发性神经根神经病(CIDP)是一种免疫介导的疾病,症状和严重程度各异,可能难以诊断。静脉注射免疫球蛋白、血浆置换和皮质类固醇在随机对照试验中均已被证明有益,尽管皮质类固醇的证据尚不明确。虽然这些治疗方法的疗效可能相似,但在成本、可用性和不良反应方面存在差异。在决定为患者提供哪种治疗时,应考虑这些特征。如果对第一种治疗方案无反应,则应尝试其他治疗方法之一。纯运动型CIDP患者在接受皮质类固醇治疗后可能会恶化。一些患者对这些传统治疗无反应或变得难治或不耐受。对治疗无反应的患者应再次检查是否出现单克隆蛋白或其他恶性肿瘤迹象。多年来,小型非随机研究报告了各种免疫抑制剂可能的有益效果。一项Cochrane综述得出结论,目前尚无足够证据确定这些免疫抑制药物对CIDP是否有益。使用免疫抑制药物时,应意识到有些药物甚至可能导致脱髓鞘疾病。由于这些新治疗方法仅在一小部分对其他治疗难治的患者中使用,且通常与其他治疗联合使用,因此很难证明其有益效果。CIDP患者在感染期间或感染后可能会恶化或自发改善,这使得判断治疗效果更加困难。文中描述了CIDP的各种治疗方法,如硫唑嘌呤、环孢素、环磷酰胺、干扰素、甲氨蝶呤、霉酚酸酯、利妥昔单抗和依那西普。根据先前的报告及其证据水平,对这些新治疗方法、作用方式、不良反应以及在CIDP治疗谱中的潜在地位进行了概述。