Department of Pharmaceutical Health Outcomes and Policy, College of Pharmacy, University of Houston, TX, USA.
Baylor College of Medicine, Houston, TX, USA.
Mult Scler Relat Disord. 2024 Nov;91:105896. doi: 10.1016/j.msard.2024.105896. Epub 2024 Sep 19.
With multiple treatment options, choosing the initial disease-modifying agent (DMA) could be crucial to managing multiple sclerosis (MS). Common treatment strategies recommend starting patients with moderate-efficacy disease-modifying agents (meDMAs), while others advocate initiating high-efficacy disease-modifying agents (heDMAs). However, limited real-world evidence exists regarding the factors associated with utilizing differing treatment strategies in the MS.
This study evaluated the factors associated with the initiation of heDMAs in comparison to meDMAs among patients with MS.
A retrospective cohort study was conducted using the Merative MarketScan Commercial Claims Database. Adult (18-64 years) MS patients with ≥1 DMA prescription were identified from 2016 to 2019. Patients were classified as incident heDMA or meDMA users based on their earliest DMA prescription, with a 12-month washout period. All covariates were measured during the 12-month baseline before the index DMA date. A multivariable logistic regression model, guided by the Andersen Behavioral Model, was applied to examine the predisposing, enabling, and need factors associated with using heDMAs over meDMAs.
There were 10,003 eligible MS patients, with the majority of users being female (74.92 %), middle-aged adults (35-54 years, 58.97 %), and enrolled in the Preferred Provider Organization (PPO, 53.10 %) healthcare plan. Overall, 2293 (22.92 %) MS patients initiated heDMAs. The multivariable logistic regression model revealed that male patients (adjusted odds ratio [aOR]: 1.46, 95 % Confidence Interval [CI]: 1.30-1.64) had higher odds of initiating heDMAs. Meanwhile, patients with bladder dysfunction medications (aOR: 1.39, 95% CI: 1.21-1.61), fatigue medications (aOR: 1.77, 95 %CI: 1.44-2.17), and impaired walking (aOR: 1.62, 95 %CI: 1.42-1.86) were more likely to initiate treatment with heDMAs. In contrast, patients with higher Elixhauser comorbidities scores, sensory symptoms (aOR: 0.47, 95 %CI: 0.42-0.53), visual symptoms (aOR: 0.63, 95 %CI: 0.54-0.73), and brainstem symptoms (aOR: 0.81, 95 %CI: 0.67-0.97) were less likely to be prescribed with heDMAs.
The study found that approximately one in four MS patients initiated heDMAs. Both demographic and clinical factors influenced the selection of heDMA. More work is needed to understand the differential value of selecting heDMAs over meDMAs for personalizing DMA treatment.
由于有多种治疗选择,选择初始疾病修正治疗药物(DMA)可能对管理多发性硬化症(MS)至关重要。常见的治疗策略建议使用中度疗效的疾病修正治疗药物(meDMA)开始治疗患者,而其他策略则主张使用高效力的疾病修正治疗药物(heDMA)。然而,关于 MS 患者使用不同治疗策略的相关因素,实际证据有限。
本研究评估了与 meDMA 相比,MS 患者使用 heDMA 的相关因素。
本研究使用 Merative MarketScan 商业索赔数据库进行了一项回顾性队列研究。从 2016 年至 2019 年,确定了≥1 种 DMA 处方的成年(18-64 岁)MS 患者。根据最早的 DMA 处方,将患者分类为 heDMA 或 meDMA 的初治使用者,采用 12 个月的洗脱期。所有协变量均在 DMA 索引日期前的 12 个月基线期内测量。基于安德森行为模型的多变量逻辑回归模型用于检查与使用 heDMA 而非 meDMA 相关的倾向、使能和需求因素。
共有 10003 名符合条件的 MS 患者,其中大多数患者为女性(74.92%),中年成年人(35-54 岁,58.97%),并参加了首选提供者组织(PPO,53.10%)的医疗保健计划。总体而言,有 2293 名(22.92%)MS 患者开始使用 heDMA。多变量逻辑回归模型显示,男性患者(调整后的优势比[aOR]:1.46,95%置信区间[CI]:1.30-1.64)更有可能开始使用 heDMA。同时,有膀胱功能障碍药物(aOR:1.39,95%CI:1.21-1.61)、疲劳药物(aOR:1.77,95%CI:1.44-2.17)和行走障碍(aOR:1.62,95%CI:1.42-1.86)的患者更有可能开始使用 heDMA 治疗。相比之下,Elixhauser 合并症评分较高、有感觉症状(aOR:0.47,95%CI:0.42-0.53)、视觉症状(aOR:0.63,95%CI:0.54-0.73)和脑干症状(aOR:0.81,95%CI:0.67-0.97)的患者不太可能被处方 heDMA。
研究发现,大约四分之一的 MS 患者开始使用 heDMA。人口统计学和临床因素均影响 heDMA 的选择。需要进一步研究,以了解为实现 DMA 治疗的个体化而选择 heDMA 而非 meDMA 的差异价值。