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超越传统疗法:生物制剂及其他新型疗法的作用

Transcending conventional therapies: the role of biologic and other novel therapies.

作者信息

Sandborn W J

机构信息

Mayo Medical School, Rochester, Minnesota 55905, USA.

出版信息

Inflamm Bowel Dis. 2001 May;7 Suppl 1:S9-16. doi: 10.1002/ibd.3780070504.

Abstract

Biologic and other novel therapies targeted to specific pathogenic processes offer the potential for improved treatment outcomes in patients with Crohn's disease and alteration of the course of the disease. Therapies targeted to tumor necrosis factor alpha (TNF-alpha) include anti-TNF-alpha monoclonal antibodies (infliximab and CDP-571), TNF-binding neutralizing fusion proteins (etanercept), and TNF-alpha production inhibitors (thalidomide). In placebo-controlled trials, infliximab has rapidly induced clinical response and remission in patients with moderately to severely active Crohn's disease refractory to conventional therapy and patients with fistulizing Crohn's disease, with minimal toxicity; retreatment with infliximab in patients who experienced an initial response maintained their clinical improvement. Clinical experience suggests that infliximab may also be effective when administered as corticosteroid-sparing therapy. Infliximab is the only anti-TNF-alpha therapy currently available in clinical practice for the treatment of active Crohn's disease. Controlled trials of the investigational anti-TNF-alpha agent CDP-571 show benefit for induction of clinical improvement and steroid-sparing, but further investigation is needed. A pilot study of etanercept suggested a beneficial effect, but its efficacy was not confirmed in a controlled trial. In open-label trials, thalidomide has demonstrated efficacy in patients with refractory Crohn's disease; however, the therapeutic potential of thalidomide may be severely limited by the high incidence of drug-induced side effects. Other novel agents, including anti-alpha4 integrin antibodies, interleukin (IL)-10 and IL-11, and the immunomodulators tacrolimus and mycophenolate mofetil have been evaluated as treatment in patients with severely active or fistulizing Crohn's disease in open-label and controlled trials, with varied results reported to date. The development of these new therapies is an exciting advance that promises to improve the management of Crohn's disease and expand current knowledge of underlying pathophysiologic mechanisms.

摘要

针对特定致病过程的生物制剂和其他新型疗法为改善克罗恩病患者的治疗效果及改变疾病进程提供了可能。针对肿瘤坏死因子α(TNF-α)的疗法包括抗TNF-α单克隆抗体(英夫利昔单抗和CDP-571)、TNF结合中和融合蛋白(依那西普)以及TNF-α产生抑制剂(沙利度胺)。在安慰剂对照试验中,英夫利昔单抗能迅速使常规治疗无效的中度至重度活动性克罗恩病患者以及瘘管性克罗恩病患者产生临床反应并实现缓解,且毒性极小;对初始有反应的患者再次使用英夫利昔单抗可维持其临床改善效果。临床经验表明,英夫利昔单抗作为糖皮质激素节省疗法使用时可能也有效。英夫利昔单抗是目前临床实践中唯一可用于治疗活动性克罗恩病的抗TNF-α疗法。对研究性抗TNF-α药物CDP-571的对照试验显示其对诱导临床改善和节省类固醇有益,但仍需进一步研究。依那西普的一项初步研究提示有有益作用,但其疗效在对照试验中未得到证实。在开放标签试验中,沙利度胺已证明对难治性克罗恩病患者有效;然而,沙利度胺的治疗潜力可能因药物诱导的副作用发生率高而受到严重限制。其他新型药物,包括抗α4整合素抗体、白细胞介素(IL)-10和IL-11,以及免疫调节剂他克莫司和霉酚酸酯,已在开放标签和对照试验中作为重度活动性或瘘管性克罗恩病患者的治疗方法进行了评估,迄今报告的结果各不相同。这些新疗法的开发是一项令人兴奋的进展,有望改善克罗恩病的管理并扩展当前对潜在病理生理机制的认识。

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