Cocco Eleonora, Marchi Piernicola, Floris Gianluca, Mascia Maria Giuseppina, Deriu Marcello, Sirca Antonella, Mamusa Elena, Lai Marina, Mura Marco, Mallarini Giorgio, Marrosu Maria Giovanna
Multiple Sclerosis Centre, Binaghi Hospital, Department of Cardiovascular and Neurological Sciences, University of Cagliari, Italy.
Funct Neurol. 2006 Jul-Sep;21(3):145-9.
There is still debate over the optimal dosage, frequency and route of administration of interferon (IFN) beta in multiple sclerosis (MS). A prospective, non-randomized, comparative study was performed to evaluate differences in magnetic resonance imaging and clinical outcomes of two IFN beta-1a preparations (30mcg intramuscular [im] once-weekly [qw], AVO; and 22 mcg subcutaneous [sc] three-times-weekly [tiw]; R22). Relapsing-remitting MS patients on one of the two IFN preparations (AVO, n=47; R22, n=48) were assessed at baseline and after 6 months of further treatment. There were no significant differences between the two groups at baseline. Both groups showed significantly reduced relapse rates (F=19.5; p<0.001) from baseline (0.6) to 6-month assessment (0.2; p<0.001). Univariate analysis showed a significant difference in favour of R22 on T2 lesion volume (F=14.4; p<0.001) and T1 black hole lesion load (F=8.5; p=0.004), the latter showing a significant increase in the AVO group (p<0.001). The incidence of patients with new T1 black holes was also higher for AVO than R22 (23.5% vs 8.3%; p=0.025). These results from patients receiving AVO or R22 in normal clinical practice are in line with randomized clinical studies that show the benefits of high-dose, high-frequency administration of IFN beta-1a in MS therapy.
在多发性硬化症(MS)中,关于β-干扰素(IFN)的最佳剂量、给药频率和途径仍存在争议。进行了一项前瞻性、非随机、对照研究,以评估两种β-1a干扰素制剂(30微克肌肉注射[im],每周一次[qw],AVO;以及22微克皮下注射[sc],每周三次[tiw];R22)在磁共振成像和临床结果方面的差异。对接受这两种干扰素制剂之一治疗的复发缓解型MS患者(AVO组,n = 47;R22组,n = 48)在基线期和进一步治疗6个月后进行评估。两组在基线期无显著差异。两组从基线期(0.6)到6个月评估时的复发率均显著降低(F = 19.5;p < 0.001)(0.2;p < 0.001)。单因素分析显示,在T2病变体积(F = 14.4;p < 0.001)和T1黑洞病变负荷方面,R22组有显著优势(F = 8.5;p = 0.004),后者在AVO组有显著增加(p < 0.001)。AVO组新出现T1黑洞的患者发生率也高于R22组(23.5%对8.3%;p = 0.025)。这些在正常临床实践中接受AVO或R22治疗的患者的结果与随机临床研究一致,这些研究表明高剂量、高频给药的β-1a干扰素在MS治疗中的益处。