Queensland University of Technology, Faculty of Science and Technology, GPO 2343, QLD 4001, Brisbane, Australia.
Expert Opin Pharmacother. 2010 Jul;11(10):1777-81. doi: 10.1517/14656566.2010.481671.
Most people with multiple sclerosis (MS) have the relapsing-remitting type. The objective was to evaluate two clinical trials of fingolimod in relapsing MS. FREEDOMS (FTY720 Research Evaluation Effects of Daily Oral therapy in Multiple Sclerosis), a Phase III placebo-controlled trial, showed that fingolimod (0.5 or 1.25 mg) reduced the relapse rate and disability in MS, compared with placebo. Fingolimod (0.5 or 1.25 mg) has been compared to interferon-beta-1a in a Phase III clinical trial (TRANSFORMS; Trial Assessing Injectable Interferon versus FTY720 Oral in Relapsing-Remitting Multiple Sclerosis) and shown to be more efficacious than interferon-beta-1a in reducing relapse rates. However, fingolimod did increase the risk of infections and skin cancers. Only the lower dose of fingolimod (0.5 mg), which possibly has less toxicity, should be considered for prevention of relapses in relapsing-remitting MS.
大多数多发性硬化症(MS)患者为复发缓解型。本研究旨在评估两种用于复发型 MS 的芬戈莫德临床试验。FREEDOMS(FTY720 Research Evaluation Effects of Daily Oral therapy in Multiple Sclerosis)是一项 III 期安慰剂对照试验,结果表明与安慰剂相比,芬戈莫德(0.5 或 1.25mg)可降低 MS 的复发率和残疾程度。芬戈莫德(0.5 或 1.25mg)已在一项 III 期临床试验(TRANSFORMS;试验评估注射用干扰素-β-1a 与 FTY720 口服剂在复发缓解型多发性硬化症中的疗效)中与干扰素-β-1a 进行了比较,结果表明其在降低复发率方面比干扰素-β-1a 更有效。然而,芬戈莫德确实增加了感染和皮肤癌的风险。只有毒性可能较低的较低剂量(0.5mg)的芬戈莫德才应考虑用于预防复发缓解型 MS 的复发。