美国青少年重症肌无力的治疗模式与疾病负担:一项使用医疗保健理赔数据库的队列研究
Treatment Patterns and Disease Burden of Juvenile Myasthenia Gravis in the United States: A Cohort Study Using Health Care Claims Databases.
作者信息
Zhou Jiachen, Nilius Sigrid, Pilipczuk Olga, Scowcroft Anna, Tarancón Thaïs, Tennigkeit Frank, Zaremba Piotr, Chandra Nishtha, Kuntz Nancy, Strober Jonathan, Brandsema John
机构信息
UCB, Cambridge, MA.
UCB, Monheim, Germany.
出版信息
Neurology. 2025 Jul 8;105(1):e213736. doi: 10.1212/WNL.0000000000213736. Epub 2025 Jun 9.
BACKGROUND AND OBJECTIVES
Juvenile myasthenia gravis (JMG) is a rare disorder defined as MG in patients younger than 18 years. Generalized JMG is more common in postpubertal than prepubertal patients. There are no formal international JMG treatment guidelines, and knowledge on treatment patterns and disease burden is limited. The aim of this study was to describe treatment patterns and health care resource utilization (HCRU) for patients with JMG and explore differences in disease presentation between prepubertal-onset (younger than 12 years) and postpubertal-onset (12-17 years) patients.
METHODS
Patients with JMG, newly diagnosed from 2008 to 2021, were identified from the US Merative MarketScan® Research Databases. Patients were followed from the first JMG claim (diagnosis/treatment with acetylcholinesterase inhibitors, immunoglobulin [Ig], or plasma exchange [PLEX]). The primary outcome was JMG-related treatment changes during follow-up, assessed descriptively. Rates of MG exacerbation, thymectomy, and acute intravenous immunoglobulin/PLEX treatment were assessed. HCRU was evaluated.
RESULTS
A total of 630 patients (64.1% female; mean [SD] age 9.07 [5.73] years; 57.6% prepubertal onset) were followed for a median (range) of 2.4 (0-13) years. Corticosteroids were started at a median (range) of 1.28 (0-37.02) and 3.19 (0-87.68) months from diagnosis for postpubertal-onset and prepubertal-onset patients, respectively. The rate of thymectomy was highest during treatment with maintenance Ig/PLEX (incidence rate [IR]; [95% CI] per 100 patient-years: 34.62 [14.41-83.17] for postpubertal-onset and 24.24 [9.10-64.60] for prepubertal-onset patients). MG exacerbations were most frequent during the first year of follow-up in both subgroups (34.1% and 30.3%). In postpubertal-onset patients, exacerbation was highest during treatment with maintenance Ig/PLEX and nonsteroid immunosuppressant therapy ([NSIST], mostly polytherapy) (IR [95% CI] 105.81 [68.99-162.29] and 91.22 [65.80-126.47]). For prepubertal-onset patients, exacerbation was most frequent during NSIST (polytherapy) and biologic treatment (IR [95% CI] 140.44 [115.45-170.85] and 142.95 [46.10-443.23]). JMG-related hospitalizations occurred in 36.0% and 30.0% of postpubertal-onset and prepubertal-onset patients, in the first year of follow-up.
DISCUSSION
Patients with JMG escalated rapidly through the treatment hierarchy. Postpubertal-onset patients escalated more quickly to later-line treatments than prepubertal-onset patients. However, some patients continued to experience high HCRU, highlighting the need for new JMG treatments to provide rapid disease control. A limitation is that treatment escalation reasons were not evaluated.
背景与目的
青少年重症肌无力(JMG)是一种罕见疾病,定义为18岁以下患者患有的重症肌无力。全身性JMG在青春期后发病的患者中比青春期前发病的患者更常见。目前尚无正式的国际JMG治疗指南,关于治疗模式和疾病负担的知识有限。本研究的目的是描述JMG患者的治疗模式和医疗资源利用(HCRU)情况,并探讨青春期前发病(12岁以下)和青春期后发病(12 - 17岁)患者在疾病表现上的差异。
方法
从美国默克公司的MarketScan®研究数据库中识别出2008年至2021年新诊断的JMG患者。从首次JMG索赔(使用乙酰胆碱酯酶抑制剂、免疫球蛋白[Ig]或血浆置换[PLEX]进行诊断/治疗)开始对患者进行随访。主要结局是随访期间与JMG相关的治疗变化,采用描述性评估。评估重症肌无力加重、胸腺切除术以及急性静脉注射免疫球蛋白/PLEX治疗的发生率。对HCRU进行评估。
结果
共随访了630例患者(64.1%为女性;平均[标准差]年龄9.07[5.73]岁;57.6%为青春期前发病),中位(范围)随访时间为2.4(0 - 13)年。青春期后发病和青春期前发病的患者分别在诊断后的中位(范围)1.28(0 - 37.02)个月和3.19(0 - 87.68)个月开始使用糖皮质激素。在维持Ig/PLEX治疗期间胸腺切除术的发生率最高(发病率[IR];[95%置信区间]每100患者年:青春期后发病患者为34.62[14.41 - 83.17],青春期前发病患者为24.24[9.10 - 64.60])。在两个亚组中,重症肌无力加重在随访的第一年最为频繁(分别为34.1%和30.3%)。在青春期后发病的患者中,在维持Ig/PLEX和非甾体免疫抑制剂治疗([NSIST],大多为联合治疗)期间加重发生率最高(IR[95%置信区间]105.81[68.99 - 162.29]和91.22[65.80 - 126.47])。对于青春期前发病的患者,在NSIST(联合治疗)和生物治疗期间加重最为频繁(IR[95%置信区间]140.44[115.45 - 170.85]和142.95[46.10 - 443.23])。在随访的第一年,青春期后发病和青春期前发病的患者中分别有36.0%和30.0%发生与JMG相关的住院治疗。
讨论
JMG患者在治疗分级中迅速升级。青春期后发病的患者比青春期前发病的患者更快升级到后续治疗。然而,一些患者继续经历较高水平的HCRU,这突出表明需要新的JMG治疗方法来实现快速的疾病控制。一个局限性是未评估治疗升级的原因。