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回顾性评价利妥昔单抗治疗进展性和有症状性纤维性纵隔炎患者的疗效。

A Retrospective Evaluation of the Treatment Effects of Rituximab in Patients with Progressive and Symptomatic Fibrosing Mediastinitis.

机构信息

Division of Pulmonary and Department of Critical Care Medicine, Mayo Clinic, Phoenix, Arizona; and.

Department of Radiology.

出版信息

Ann Am Thorac Soc. 2024 Nov;21(11):1533-1541. doi: 10.1513/AnnalsATS.202405-533OC.

Abstract

Fibrosing mediastinitis (FM) is an uncommon fibroinflammatory condition without established or effective medical therapies. Infiltrating B lymphocytes are commonly present, and progressive fibrosis compromises mediastinal structures, including blood vessels and airways, resulting in significant morbidity and mortality. To evaluate the benefits and side effects of rituximab in patients with progressive and symptomatic FM. We treated 22 patients (median age, 35 yr; range, 15-68 yr; 45% female) with metabolically active, progressive FM with rituximab on an off-label basis. Additionally, patients were administered pneumocystis and antifungal prophylaxis when immunosuppressed with rituximab. Modeling of longitudinal treatment response based on changes in relative lesion volume from baseline was performed retrospectively using functional data analysis, and time-to-event modeling was performed to estimate treatment response rates based on a >30% reduction in pretreatment volume. The primary endpoints were lack of disease progression and change in mediastinal lesion volume on computed tomography (evaluated retrospectively). No patient experienced disease progression after rituximab therapy. Median clinical follow-up was 42 months (range, 7-94 mo) and imaging follow-up 21 months (range, 7-62 mo). A total of 82% of patients had confirmed histoplasmosis-associated FM. After rituximab treatment, a 49.6% (95% confidence interval, 17.5-64.4%) mean estimated decrease in pretreatment lesion volume was observed at 24 months. The estimated objective treatment response rate was 47.9% (95% confidence interval, 26.7-70.3%). This observational study suggests that rituximab is a well tolerated and potentially effective therapy in a cohort of patients with symptomatic and progressive FM.

摘要

纤维性纵隔炎(FM)是一种罕见的纤维性炎症性疾病,目前尚无确定或有效的医学治疗方法。浸润性 B 淋巴细胞通常存在,进行性纤维化会损害纵隔结构,包括血管和气道,导致发病率和死亡率显著增加。为了评估利妥昔单抗在进展性和有症状的 FM 患者中的益处和副作用。我们对 22 名(中位年龄 35 岁;范围 15-68 岁;45%为女性)代谢活跃、进行性 FM 患者进行了利妥昔单抗治疗,这是一种基于标签外的治疗。此外,在使用利妥昔单抗进行免疫抑制时,患者还接受了卡氏肺孢子虫和抗真菌预防。使用功能数据分析对基于基线相对病变体积变化的纵向治疗反应进行了回顾性建模,并进行时间事件建模以根据预处理体积减少>30%来估计治疗反应率。主要终点是无疾病进展和 CT 上纵隔病变体积的变化(回顾性评估)。利妥昔单抗治疗后,没有患者出现疾病进展。中位临床随访时间为 42 个月(范围 7-94 个月),影像学随访时间为 21 个月(范围 7-62 个月)。共有 82%的患者确诊为组织胞浆菌相关性 FM。利妥昔单抗治疗后 24 个月,预处理病变体积平均估计减少 49.6%(95%置信区间,17.5-64.4%)。估计的客观治疗反应率为 47.9%(95%置信区间,26.7-70.3%)。这项观察性研究表明,利妥昔单抗是一种在有症状和进行性 FM 患者中耐受性良好且潜在有效的治疗方法。

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