From the Queen Mary University London (R.D., K.S., G.G.), Blizard Institute, UK; Neurological Institute (R.A.R.), Mellen Center for MS Treatment and Research, Cleveland, OH; and Royal London Hospital (R.D., B.T., K.S., G.G.), Barts Health NHS Trust, UK.
Neurology. 2014 Jan 21;82(3):248-54. doi: 10.1212/WNL.0000000000000036. Epub 2013 Dec 11.
Interferon-β (IFN-β) has been shown to reduce relapse rates in multiple sclerosis; however, the clinical response appears to vary among individuals. Can early MRI be used to identify those patients who have a poor response to treatment?
A systematic review of studies examining differential treatment response and clinical endpoints in groups defined as responders or nonresponders to IFN-β was performed. Meta-analytic techniques were used to combine study results where appropriate.
Patients with MRI evidence of poor response to IFN-β treatment as defined by either ≥2 new hyperintense T2 lesions or new gadolinium-enhancing lesions had significantly increased risk of both future relapses and progression as defined by the Expanded Disability Status Scale. There appeared to be an increased risk of poor outcomes 16 years after treatment initiation in those with an initial poor response to treatment. Previous evidence has shown this not to be the case in placebo arms of clinical trials.
For those patients starting IFN-β, early MRI, within 6 to 24 months after starting treatment, has the potential to provide important information when counseling patients about the likelihood of future treatment failure. This can inform treatment decisions before clinical relapses or disease progression.
干扰素-β(IFN-β)已被证明可降低多发性硬化症的复发率;然而,临床反应似乎因人而异。早期 MRI 是否可用于识别那些对治疗反应不佳的患者?
对检查 IFN-β治疗反应不同和根据应答者或无应答者定义的临床终点的研究进行系统评价。在适当的情况下,使用荟萃分析技术合并研究结果。
根据是否存在≥2 个新的高信号 T2 病变或新的钆增强病变,MRI 显示对 IFN-β治疗无应答的患者在未来复发和扩展残疾状况量表定义的进展方面的风险显著增加。在开始治疗后 16 年,那些初始治疗无应答的患者出现不良结局的风险似乎增加。先前的证据表明,在临床试验的安慰剂组中并非如此。
对于开始接受 IFN-β治疗的患者,在开始治疗后 6 至 24 个月内进行早期 MRI,当向患者提供关于未来治疗失败可能性的信息时,具有提供重要信息的潜力。这可以在临床复发或疾病进展之前为治疗决策提供依据。