Neutropenia Associated With B Cell-Depleting Therapies in Multiple Sclerosis and Neuromyelitis Optica Spectrum Disorder.

IF 7.5 1区 医学 Q1 CLINICAL NEUROLOGY
Greer Waldrop, Nikki Sisodia, Shane Poole, Samuel Pleasure, Michael R Wilson, Chu-Yueh Guo, Jeffrey M Gelfand, Scott S Zamvil, Riley Bove
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引用次数: 0

Abstract

Background and objectives: Neutropenia is described as a rare adverse event associated with B cell-depleting therapy (BCDT) use in patients with multiple sclerosis (MS) and neuromyelitis optica spectrum disorder (NMOSD). However, little is known about longitudinal clinical outcomes. We estimated the real-world incidence of neutropenia among patients with neuroinflammatory disease treated with BCDT and characterized the clinical course.

Methods: We conducted a retrospective cohort study using electronic medical records to estimate the incidence rate of neutropenia in adults with MS/NMOSD from a neuroimmunology clinic in California between January 6, 2006, and November 2, 2015, treated with ocrelizumab, rituximab, ofatumumab, ublituximab, or inebilizumab. Each clinical course (recurrence, time to recovery of absolute neutrophil count [ANC], postneutropenia treatment) of neutropenia was then presented in a case series.

Results: In this cohort of 1,825 patients (6,009 person-years on BCDT), the largest cohort addressing this question to date, 37 developed neutropenia. The estimated incidence rate of neutropenia was 0.62 (95% CI 0.45-0.85) per 100 person-years. The median time from last infusion of current BCDT was 4 months (interquartile range [IQR] 1-6). The median nadir ANC was 390 (IQR 40-960); the nadir ANC was 0 for 6 patients (16%). All patients ultimately recovered to normal counts, except 2 patients developing fluctuating ANCs for months. Among the 32 patients not receiving filgrastim, the median time to ANC recovery was 11 days (95% CI 7-26). Course severity was asymptomatic/mild in 32% (n = 12) while 54% (n = 20) required hospitalization. A confirmed simultaneous infection or infectious prodrome occurred in 23 (62%). After recovery, 30 patients (81%) continued BCDT and 2 (7%) changed within BCDT class. Neutropenia recurred in 13 patients (35%), including 3 who discontinued BCDT after initial neutropenia. The estimated incidence rate of recurrent neutropenia was 0.22 (95% CI 0.13-0.39) per 100 person-years. The mean (SD) time to recurrence from initial neutropenia was 251 (SD: 355) days.

Discussion: This study is comprehensive and reflects a large cohort, examining incidence rates of neutropenia with BCDT in MS and NMOSD. Overall, neutropenia was still rare, occurring at a rate of 0.66 per 100 person-years, and infections were associated triggers in some patients. Yet, of relevance to clinicians, neutropenia was not benign: half required hospitalization and 35% experienced recurrence, which is higher than what was reported in clinical trials.

中性粒细胞减少与B细胞消耗疗法在多发性硬化症和视谱障碍神经脊髓炎中的相关性。
背景和目的:中性粒细胞减少症是一种罕见的不良事件,与B细胞消耗疗法(BCDT)用于多发性硬化症(MS)和视神经脊髓炎谱系障碍(NMOSD)患者相关。然而,对纵向临床结果知之甚少。我们估计了接受BCDT治疗的神经炎性疾病患者中性粒细胞减少症的真实发生率,并描述了临床过程。方法:我们进行了一项回顾性队列研究,使用电子医疗记录来估计2006年1月6日至2015年11月2日期间,在加州一家神经免疫学诊所接受ocrelizumab、rituximab、ofatumumab、ublituximab或inebilizumab治疗的成年MS/NMOSD患者中性粒细胞减少的发生率。中性粒细胞减少的每个临床过程(复发、绝对中性粒细胞计数[ANC]恢复时间、中性粒细胞减少后治疗)随后被记录在一个病例系列中。结果:在这个包含1825名患者(6009人年BCDT治疗)的队列中,37名患者出现了中性粒细胞减少症,这是迄今为止研究该问题的最大队列。中性粒细胞减少的估计发病率为每100人年0.62 (95% CI 0.45-0.85)。距最后一次输注当前BCDT的中位时间为4个月(四分位数间距[IQR] 1-6)。中位最低点ANC为390 (IQR 40-960);6例(16%)患者的最低ANC为0。所有患者最终计数恢复正常,除了2例患者出现数月波动的anc。在32名未接受非格昔汀治疗的患者中,ANC恢复的中位时间为11天(95% CI 7-26)。病程严重程度为无症状/轻度的占32% (n = 12),需要住院治疗的占54% (n = 20)。23例(62%)发生确诊的同时感染或感染性前驱症状。康复后,30例(81%)患者继续接受BCDT治疗,2例(7%)患者改变BCDT治疗类别。13例(35%)患者中性粒细胞减少复发,其中3例在初始中性粒细胞减少后停用BCDT。复发性中性粒细胞减少的估计发生率为每100人年0.22 (95% CI 0.13-0.39)。从初始中性粒细胞减少到复发的平均(SD)时间为251 (SD: 355)天。讨论:这项研究是全面的,反映了一个大的队列,研究了MS和NMOSD中中性粒细胞减少症合并BCDT的发病率。总的来说,中性粒细胞减少症仍然很少见,发生率为每100人年0.66例,感染是一些患者的相关诱因。然而,与临床医生相关的是,中性粒细胞减少症不是良性的:一半的患者需要住院治疗,35%的患者复发,这比临床试验中报道的要高。
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来源期刊
CiteScore
15.60
自引率
2.30%
发文量
219
审稿时长
8 weeks
期刊介绍: Neurology Neuroimmunology & Neuroinflammation is an official journal of the American Academy of Neurology. Neurology: Neuroimmunology & Neuroinflammation will be the premier peer-reviewed journal in neuroimmunology and neuroinflammation. This journal publishes rigorously peer-reviewed open-access reports of original research and in-depth reviews of topics in neuroimmunology & neuroinflammation, affecting the full range of neurologic diseases including (but not limited to) Alzheimer's disease, Parkinson's disease, ALS, tauopathy, and stroke; multiple sclerosis and NMO; inflammatory peripheral nerve and muscle disease, Guillain-Barré and myasthenia gravis; nervous system infection; paraneoplastic syndromes, noninfectious encephalitides and other antibody-mediated disorders; and psychiatric and neurodevelopmental disorders. Clinical trials, instructive case reports, and small case series will also be featured.
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