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IL-6 靶向治疗时代特发性多中心 Castleman 病的流行病学和治疗模式。

Epidemiology and treatment patterns of idiopathic multicentric Castleman disease in the era of IL-6-directed therapy.

机构信息

Department of Hematology and Medical Oncology, Taussig Cancer Institute, Cleveland Clinic, Cleveland, OH.

EUSA Pharma, Burlington, MA.

出版信息

Blood Adv. 2022 Jan 25;6(2):359-367. doi: 10.1182/bloodadvances.2021004441.

Abstract

The epidemiology of human herpesvirus-8-negative/idiopathic multicentric Castleman disease (iMCD) remains incompletely understood. Prior epidemiologic studies of CD and iMCD have been hampered by difficulties in accurate case ascertainment resulting from a lack of uniform diagnostic criteria and a disease-specific International Classification of Diseases (ICD) code. In this study, we provide reliable estimates of CD and iMCD in the United States using a novel claims-based algorithm that includes a CD-specific ICD (10th revision) diagnosis code (D47.Z2) supported by the presence of ≥2 claims codes corresponding to the minor criteria from the international evidence-based diagnostic criteria for iMCD. We additionally analyzed the treatment classes and patterns in the clinical course of patients with iMCD. Using an administrative claims database of 30.7 million individuals enrolled between 1 January 2017 and 31 December 2018, we identified 254 patients with iMCD, with an estimated annual incidence and prevalence of 3.4 (95% confidence interval [CI], 1.4-9.2) and 6.9 (95% CI, 3.7-13.3) cases per million, respectively. Among patients with iMCD, 39% received corticosteroid monotherapy, 33.1% received no iMCD-directed treatment, and 9.8% received interleukin-6 (IL-6)-targeted therapy with tocilizumab or siltuximab. Siltuximab, which is the only US Food and Drug Administration-approved treatment and established first-line treatment recommendation, was used in only 8.7% of patients with iMCD. This study provides the most up-to-date understanding of the iMCD disease burden in the United States and identifies a major unmet treatment need for IL-6-directed therapy in this vulnerable cohort.

摘要

人类疱疹病毒 8 阴性/特发性多中心 Castleman 病(iMCD)的流行病学仍不完全清楚。先前的 CD 和 iMCD 流行病学研究受到准确病例确定的困难的阻碍,这是由于缺乏统一的诊断标准和特定于疾病的国际疾病分类(ICD)代码。在这项研究中,我们使用一种新的基于索赔的算法,为美国提供了 CD 和 iMCD 的可靠估计,该算法包括一个特定于 CD 的 ICD(第 10 版)诊断代码(D47.Z2),并辅以存在至少 2 个与 iMCD 的国际循证诊断标准的次要标准相对应的索赔代码。我们还分析了 iMCD 患者临床病程中的治疗类别和模式。使用 2017 年 1 月 1 日至 2018 年 12 月 31 日期间登记的 3070 万人的行政索赔数据库,我们确定了 254 例 iMCD 患者,估计每年的发病率和患病率分别为 3.4(95%置信区间[CI],1.4-9.2)和 6.9(95%CI,3.7-13.3)每百万例。在 iMCD 患者中,39%接受了皮质类固醇单药治疗,33.1%未接受 iMCD 靶向治疗,9.8%接受了托珠单抗或西妥昔单抗的 IL-6 靶向治疗。西妥昔单抗是唯一获得美国食品和药物管理局批准的治疗方法,也是一线治疗推荐方法,仅在 8.7%的 iMCD 患者中使用。这项研究提供了对美国 iMCD 疾病负担的最新了解,并确定了这一脆弱人群对 IL-6 靶向治疗的重大未满足需求。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3cf0/8791564/64662dc2e096/advancesADV2021004441absf1.jpg

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