Trojano M, Pellegrini F, Paolicelli D, Fuiani A, Zimatore G B, Tortorella C, Simone I L, Patti F, Ghezzi A, Portaccio E, Rossi P, Pozzilli C, Salemi G, Lugaresi A, Bergamaschi R, Millefiorini E, Clerico M, Lus G, Vianello M, Avolio C, Cavalla P, Iaffaldano P, Direnzo V, D'Onghia M, Lepore V, Livrea P, Comi G, Amato M P
Department of Neurological and Psychiatric Sciences University of Bari, Bari, Italy.
J Neurol Sci. 2009 Nov 15;286(1-2):109-13. doi: 10.1016/j.jns.2009.06.036. Epub 2009 Jul 16.
There are a few and conflicting results from randomised controlled trials (RCTs) pertaining to the influence of gender in response to currently used disease modifying drugs in Multiple Sclerosis (MS). Observational studies may be especially valuable for answering effectiveness questions in subgroups not studied in RCTs.
To conduct a post-marketing analysis aimed to evaluate the gender effect on Interferon beta (IFNbeta) treatment response in a cohort of relapsing (RR) MS patients.
A cohort of 2570 IFNbeta-treated RRMS was prospectively followed for up to 7 years in 15 Italian MS Centers. Cox proportional hazards regression models were used to assess gender differences for risk of reaching 1st relapse and risk of progression by 1 point on Expanded Disability Status Scale (EDSS) score. Gender effects were also explored by a propensity score (PS) matching algorithm, and a tree-growing technique.
The multivariate Cox Regression analyses showed that male patients had a significant (p=0.0097) lower risk for 1st relapse and a trend (p=0.0897) for a higher risk to reach 1 point EDSS progression than females. The PS matched multivariate Cox Regression confirmed these results. The RECPAM analysis showed that male sex conferred a significant reduction in the risk for 1st relapse (HR=0.86; 95% CI=0.76-0.98; p=0.0226) in the subgroup with a low pre-treatment number of bouts, and a significant increase in the risk for 1 point EDSS progression (HR=1.33; 95% CI: 1.00-1.76; p<0.05) in the subgroup with a delayed treatment, but a still young age at the start of treatment.
The results of this exploratory analysis seem to suggest that male patients do not respond to IFNbeta treatment in the same way of females.
关于性别对目前用于治疗多发性硬化症(MS)的疾病修正药物反应的影响,随机对照试验(RCT)得出的结果较少且相互矛盾。观察性研究对于回答RCT未研究的亚组中的有效性问题可能特别有价值。
进行一项上市后分析,旨在评估复发型(RR)MS患者队列中性别对干扰素β(IFNβ)治疗反应的影响。
在15个意大利MS中心对2570例接受IFNβ治疗的RRMS患者进行了长达7年的前瞻性随访。使用Cox比例风险回归模型评估首次复发风险和扩展残疾状态量表(EDSS)评分增加1分的进展风险的性别差异。还通过倾向评分(PS)匹配算法和树生长技术探索了性别效应。
多变量Cox回归分析表明,男性患者首次复发的风险显著降低(p = 0.0097),而达到EDSS进展1分的风险高于女性,呈趋势性(p = 0.0897)。PS匹配的多变量Cox回归证实了这些结果。RECPAM分析表明,男性在治疗前发作次数较少的亚组中,首次复发风险显著降低(HR = 0.86;95%CI = 0.76 - 0.98;p = 0.0226),而在治疗延迟但开始治疗时仍较年轻的亚组中,EDSS进展1分的风险显著增加(HR = 1.33;95%CI:1.00 - 1.76;p < 0.05)。
这项探索性分析的结果似乎表明,男性患者对IFNβ治疗的反应与女性不同。