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

Cyril Varghese, Geoffrey B Johnson, Patrick W Eiken, Eric S Edell, Ulrich Specks, Nicholas B Larson, Tobias Peikert
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Abstract

Rationale: 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. Objective: To evaluate the benefits and side effects of rituximab in patients with progressive and symptomatic FM. Methods: 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). Results: 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%). Conclusions: This observational study suggests that rituximab is a well tolerated and potentially effective therapy in a cohort of patients with symptomatic and progressive FM.

利妥昔单抗对进展性和症状性纤维性纵隔炎患者治疗效果的回顾性评估
理由纤维化纵隔炎是一种不常见的纤维炎症,没有成熟或有效的药物疗法。通常存在浸润性 B 淋巴细胞,进行性纤维化会损害纵隔结构,包括血管和气道,从而导致严重的发病率和死亡率:评估利妥昔单抗对进展性无症状纤维化纵隔炎患者的益处和副作用:我们用标签外的利妥昔单抗治疗了 22 名代谢活跃的进展性纤维性纵隔炎患者(中位年龄 35 岁,年龄范围:15-68 岁,45% 为女性)。此外,在使用利妥昔单抗进行免疫抑制时,患者还需接受肺孢子菌和抗真菌预防治疗。根据相对病灶体积与基线相比的变化,利用功能数据分析回顾性地建立了纵向治疗反应模型;根据治疗前体积减少>30%的情况,建立了时间到事件模型以估计治疗反应率:主要终点为疾病无进展和CT显示纵隔病灶体积变化(回顾性评估):主要结果: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至94个月),影像学随访时间为21个月(范围:7至62个月)。82%的患者确诊为组织胞浆菌病相关纤维化纵隔炎。经过利妥昔单抗治疗后,24个月时治疗前病变体积的平均估计降幅为49.6%(95% CI = [17.5%,64.4%])。估计客观治疗反应率为 47.9% (95% CI = [26.7%, 70.3%]):这项观察性研究表明,利妥昔单抗对有症状且病情进展的一组 FM 患者具有良好的耐受性和潜在的治疗效果。
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