Department of Dermatology, University of Rome Tor Vergata, Rome, Italy.
Dermatology. 2011;222(3):250-5. doi: 10.1159/000326111. Epub 2011 Apr 13.
In February 19, 2009, the European Medicines Agency (EMA) had recommended the suspension of the marketing authorization for efalizumab after the occurrence of cases of progressive multifocal leukoencephalopathy.
To explore the efficacy of alternative therapies for psoriasis and the health status of patients who discontinued efalizumab.
An observational study was performed on 101 patients. After the EMA communication, efalizumab was discontinued in the following 2-3 months. In agreement with the patients, we decided to either prescribe other treatments or none at all.
After 1 year, 11 patients are still not treated, 63 patients are treated with biologics, and 9 patients are treated with systemic conventional therapies.
In order to prevent rebound or relapse, various approaches are available, including cyclosporine, methotrexate and biologic therapies. Interestingly, in 11 out of 31 patients who did not receive any systemic drug, psoriasis is still under control, suggesting a long-term effect of efalizumab.
2009 年 2 月 19 日,欧洲药品管理局(EMA)建议在发生进行性多灶性白质脑病病例后暂停依氟鸟氨酸的营销授权。
探讨银屑病替代疗法的疗效及停用依氟鸟氨酸对患者健康状况的影响。
对 101 例患者进行了一项观察性研究。在 EMA 发布相关信息后,依氟鸟氨酸在接下来的 2-3 个月内被停用。根据患者的意愿,我们决定为其开其他药物或不开药。
1 年后,11 例患者仍未接受治疗,63 例患者接受了生物制剂治疗,9 例患者接受了系统常规治疗。
为了防止反弹或复发,可采用多种方法,包括环孢素、甲氨蝶呤和生物制剂治疗。有趣的是,在 31 例未接受任何系统性药物治疗的患者中,有 11 例银屑病仍得到控制,提示依氟鸟氨酸有长期疗效。