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米托蒽醌和细胞毒药物的作用机制。

Mitoxantrone and cytotoxic drugs' mechanisms of action.

机构信息

Department of Neurology, University of Colorado Denver, Aurora, CO 80045, USA.

出版信息

Neurology. 2010 Jan 5;74 Suppl 1:S41-6. doi: 10.1212/WNL.0b013e3181c97f5a.

Abstract

Evidence has suggested that early, aggressive intervention may improve both short- and long-term outcomes in patients with multiple sclerosis (MS). Cytotoxic agents may offer advantages in this setting, particularly when used as an induction or add-on therapy with immunomodulators. Immunosuppression is the mechanism of action common to all cytotoxic drugs; individual subtleties in immunoregulatory actions are likely of minor importance. In the United States, mitoxantrone is currently the only cytotoxic agent approved for the treatment of MS (secondary-progressive, progressive-relapsing, and worsening relapsing-remitting forms). Therapies in phase III development include cyclophosphamide, mycophenolate mofetil, cladribine, and teriflunomide. All these drugs have exhibited efficacy in controlled clinical trials, although the degree of benefit with respect to MRI and clinical endpoints has varied both within and among the various agents. Further investigations are needed to determine whether cytotoxic drugs represent a substantial improvement over treatments that have a more targeted impact on the immune system.

摘要

有证据表明,早期积极干预可能改善多发性硬化症(MS)患者的短期和长期预后。细胞毒性药物在这种情况下可能具有优势,特别是在与免疫调节剂联合使用作为诱导或附加治疗时。免疫抑制是所有细胞毒性药物的作用机制;免疫调节作用的个体细微差别可能不太重要。在美国,米托蒽醌是目前唯一批准用于治疗多发性硬化症(继发进展型、进展复发型和恶化复发缓解型)的细胞毒性药物。处于 III 期开发阶段的疗法包括环磷酰胺、霉酚酸酯、克拉屈滨和特立氟胺。所有这些药物在对照临床试验中均显示出疗效,尽管在 MRI 和临床终点方面的获益程度在不同药物之间以及在同一药物的不同试验中存在差异。需要进一步研究以确定细胞毒性药物是否代表对免疫系统具有更靶向作用的治疗方法的重大改进。

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