Multiple Sclerosis Centre, Dept. of Neurology and Psychiatry, S. Andrea Hospital, Sapienza University, Rome, Italy.
BMC Neurol. 2011 Feb 25;11:26. doi: 10.1186/1471-2377-11-26.
In daily clinical setting, some patients affected by relapsing-remitting Multiple Sclerosis (RRMS) are switched from the low-dose to the high-dose Interferon beta (IFNB) in order to achieve a better control of the disease.
In this observational, post-marketing study we reported the 2-year clinical outcomes of patients switched to the high-dose IFNB; we also evaluated whether different criteria adopted to switch patients had an influence on the clinical outcomes.
Patients affected by RRMS and switched from the low-dose to the high-dose IFNB due to the occurrence of relapses, or contrast-enhancing lesions (CELs) as detected by yearly scheduled MRI scans, were followed for two years. Expanded Disability Status Scale (EDSS) scores, as well as clinical relapses, were evaluated during the follow-up period.
We identified 121 patients switched to the high-dose IFNB. One hundred patients increased the IFNB dose because of the occurrence of one or more relapses, and 21 because of the presence of one or more CELs, even in absence of clinical relapses. At the end of the 2-year follow-up, 72 (59.5%) patients had a relapse, and 51 (42.1%) reached a sustained progression on EDSS score. Overall, 85 (70.3%) patients showed some clinical disease activity (i.e. relapses or disability progression) after the switch. Relapse risk after increasing the IFNB dose was greater in patients who switched because of relapses than those switched only for MRI activity (HR: 5.55, p = 0.001). A high EDSS score (HR: 1.77, p < 0.001) and the combination of clinical and MRI activity at switch raised the risk of sustained disability progression after increasing the IFNB dose (HR: 2.14, p = 0.01).
In the majority of MS patients, switching from the low-dose to the high-dose IFNB did not reduce the risk of further relapses or increased disability in the 2-year follow period.Although we observed that patients who switched only on the basis on MRI activity (even in absence of clinical attacks) had a lower risk of further relapses, larger studies are warranted before to recommend a switch algorithm based on MRI findings.
在日常临床实践中,一些患有复发缓解型多发性硬化症(RRMS)的患者会从低剂量干扰素β(IFNB)转为高剂量 IFNB,以更好地控制疾病。
在这项观察性、上市后研究中,我们报告了转为高剂量 IFNB 的患者的 2 年临床结局;我们还评估了采用不同标准转换患者是否会对临床结局产生影响。
由于复发或每年定期 MRI 扫描发现的增强病变(CELs),RRMS 患者从低剂量 IFNB 转为高剂量 IFNB,这些患者在转为高剂量 IFNB 后随访 2 年。在随访期间评估扩展残疾状况量表(EDSS)评分以及临床复发情况。
我们确定了 121 例转为高剂量 IFNB 的患者。100 例患者因 1 次或多次复发而增加 IFNB 剂量,21 例患者因存在 1 次或多次 CELs 而增加 IFNB 剂量,即使没有临床复发。在 2 年的随访结束时,72 例(59.5%)患者出现复发,51 例(42.1%)患者 EDSS 评分持续进展。总体而言,85 例(70.3%)患者在转换后出现了一些临床疾病活动(即复发或残疾进展)。在因复发而增加 IFNB 剂量的患者中,复发风险高于仅因 MRI 活动而增加 IFNB 剂量的患者(HR:5.55,p = 0.001)。高 EDSS 评分(HR:1.77,p < 0.001)和转换时的临床和 MRI 活动联合增加了增加 IFNB 剂量后持续残疾进展的风险(HR:2.14,p = 0.01)。
在大多数 MS 患者中,在 2 年的随访期间,从低剂量转为高剂量 IFNB 并不能降低进一步复发或残疾加重的风险。尽管我们观察到仅基于 MRI 活动(即使没有临床发作)而转换的患者复发风险较低,但仍需要更大规模的研究来推荐基于 MRI 发现的转换算法。