Conway Devon S, Hersh Carrie M, Harris Haleigh C, Hua Le H
Mellen Center for Multiple Sclerosis Treatment and Research, Cleveland Clinic Foundation, USA.
Lou Ruvo Center for Brain Health, Cleveland Clinic Foundation, USA.
Mult Scler J Exp Transl Clin. 2020 Jan 27;6(1):2055217320902488. doi: 10.1177/2055217320902488. eCollection 2020 Jan-Mar.
To determine multiple sclerosis patient characteristics that predict a shorter duration of natalizumab treatment.
The Tysabri Outreach: Unified Commitment to Health database was reviewed to identify patients treated with natalizumab at our centers. Cox proportional hazards models were used to evaluate patient characteristics associated with shorter treatment durations on natalizumab. Associations were also assessed with respect to specific reasons for stopping natalizumab.
We identified 554 patients who began and stopped natalizumab treatment during the observation period. The average disease duration at natalizumab initiation was 7.6 years, and the average number of infusions was 30. The multivariable Cox proportional hazards model identified greater age ( = 0.035), longer disease duration ( < 0.001), progressive relapsing multiple sclerosis phenotype ( = 0.003), current smoking ( = 0.031), and greater depression ( = 0.026) as significant predictors for natalizumab discontinuation. Greater disability levels ( = 0.022) and gadolinium-enhancing lesions on baseline magnetic resonance imaging ( < 0.001) were significantly associated with longer natalizumab treatment. Individuals with progressive relapsing multiple sclerosis had a 14-fold increased hazard of discontinuing natalizumab due to inflammatory events ( < 0.001) than those with relapsing-remitting multiple sclerosis. Smokers had an 80% increased hazard of discontinuation due to intolerance ( = 0.008).
Our results suggest that smoking, depression, and a progressive relapsing multiple sclerosis phenotype are associated with shorter natalizumab treatment durations.
确定可预测那他珠单抗治疗疗程较短的多发性硬化症患者特征。
对那他珠单抗拓展:健康统一承诺数据库进行回顾,以识别在我们中心接受那他珠单抗治疗的患者。采用Cox比例风险模型评估与那他珠单抗治疗疗程较短相关的患者特征。还针对停止使用那他珠单抗的具体原因评估了相关性。
我们识别出554例在观察期内开始并停止那他珠单抗治疗的患者。开始使用那他珠单抗时的平均病程为7.6年,平均输注次数为30次。多变量Cox比例风险模型确定年龄较大(=0.035)、病程较长(<0.001)、进展复发型多发性硬化症表型(=0.003)、当前吸烟(=0.031)和抑郁程度较高(=0.026)是那他珠单抗停药的显著预测因素。较高的残疾水平(=0.022)和基线磁共振成像上钆增强病灶(<0.001)与那他珠单抗治疗时间较长显著相关。进展复发型多发性硬化症患者因炎症事件停用那他珠单抗的风险(<0.001)比复发缓解型多发性硬化症患者高14倍。吸烟者因不耐受而停药的风险增加80%(=0.008)。
我们的结果表明,吸烟、抑郁和进展复发型多发性硬化症表型与那他珠单抗治疗疗程较短相关。