Rituximab therapy in severe connective tissue disease associated interstitial lung disease: A retrospective single-centre observational study.

Q3 Medicine African Journal of Thoracic and Critical Care Medicine Pub Date : 2024-10-14 eCollection Date: 2024-01-01 DOI:10.7196/AJTCCM.2024.v30i3.1431
U F Seedat, B Christian, P E Boshoff, P Gaylard, G K Schleicher
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Abstract

Background: Connective tissue disease-associated interstitial lung disease (CTD-ILD) that progresses despite first-line immunosuppressive therapy is a clinical challenge. Rituximab (RTX) is a chimeric monoclonal antibody targeted to CD20+ B cells, resulting in B-cell depletion, and has been used as a salvage therapeutic modality in severe disease.

Objectives: To investigate the therapeutic effects and safety of RTX in patients with severe CTD-ILD.

Methods: A retrospective observational analysis of patients with severe CTD-ILD treated with salvage RTX therapy and various combinations of immunomodulatory therapy at Wits Donald Gordon Medical Centre, Johannesburg, South Africa, between January 2010 and December 2020 was performed. A total of 19 patients with progressive CTD-ILD, sufficient data, and 24-month follow-up were analysed. The effects of adding salvage RTX to standard drug therapy were investigated with serial pulmonary function testing, high-resolution computed tomography (HRCT) of the chest, and World Health Organization functional class (FC) assessment.

Results: At 24-month follow-up from baseline, there was no significant deterioration in forced vital capacity (0.01 L; 95% CI -0.13 - 0.14) (p=0.91) after commencing RTX salvage therapy. Serial HRCT of the chest showed radiological disease stability or improvement in 13 of the 19 patients (68%). FC assessment showed no significant deterioration compared with baseline (p=0.083). No serious adverse drug reactions or deaths were recorded.

Conclusion: Salvage RTX therapy, in combination with various immunomodulatory treatments, resulted in disease stability in the majority of patients with severe CTD-ILD over a 24-month period.

Study synopsis: What the study adds. Connective tissue disease-associated interstitial lung disease (CTD-ILD) is a challenging clinical entity. Rituximab (RTX), a chimeric monoclonal antibody targeted to CD20+ B cells, resulting in B-cell depletion, has been suggested as a potential therapeutic modality in refractory or severe disease. A single-centre experience of RTX salvage therapy in progressive CTD-ILD is presented.Implications of the findings. This small study suggests a possible role for RTX therapy in severe or refractory CTD-ILD.

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利妥昔单抗治疗严重结缔组织病相关间质性肺疾病:一项回顾性单中心观察性研究
背景:结缔组织病相关间质性肺疾病(CTD-ILD)在一线免疫抑制治疗后仍进展是一个临床挑战。Rituximab (RTX)是一种靶向CD20+ B细胞的嵌合单克隆抗体,可导致B细胞耗竭,已被用作严重疾病的补救性治疗方式。目的:探讨RTX治疗重度CTD-ILD的疗效和安全性。方法:回顾性观察分析2010年1月至2020年12月在南非约翰内斯堡的Wits Donald Gordon医疗中心接受补补性RTX治疗和各种免疫调节治疗组合的严重CTD-ILD患者。我们分析了19例进行性CTD-ILD患者,充分的数据和24个月的随访。通过一系列肺功能测试、胸部高分辨率计算机断层扫描(HRCT)和世界卫生组织功能分级(FC)评估,研究在标准药物治疗中加入补救性RTX的效果。结果:自基线随访24个月,两组患者用力肺活量无明显下降(0.01 L;95% CI -0.13 - 0.14) (p=0.91)。胸部系列HRCT显示19例患者中13例(68%)的放射学疾病稳定或改善。FC评估显示与基线相比无明显恶化(p=0.083)。无严重药物不良反应或死亡记录。结论:补救性RTX治疗与各种免疫调节治疗相结合,在24个月的时间内,大多数严重CTD-ILD患者的疾病稳定。研究简介:研究补充了什么。结缔组织病相关间质性肺疾病(CTD-ILD)是一个具有挑战性的临床实体。Rituximab (RTX)是一种靶向CD20+ B细胞的嵌合单克隆抗体,可导致B细胞耗竭,已被认为是难治性或严重疾病的潜在治疗方式。提出了进行性CTD-ILD的RTX挽救治疗的单中心经验。研究结果的含义。这项小型研究提示RTX治疗在严重或难治性CTD-ILD中的可能作用。
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来源期刊
African Journal of Thoracic and Critical Care Medicine
African Journal of Thoracic and Critical Care Medicine Medicine-Critical Care and Intensive Care Medicine
CiteScore
1.50
自引率
0.00%
发文量
30
审稿时长
24 weeks
期刊最新文献
Pulmonary manifestations of the idiopathic inflammatory myopathies in a South African population. Rituximab therapy in severe connective tissue disease associated interstitial lung disease: A retrospective single-centre observational study. The promise of rituximab in connective tissue disease-associated interstitial lung disease. Unveiling the pulmonary burden of idiopathic inflammatory myopathies in South Africa. Vitamin D status in patients with chronic obstructive pulmonary disease at Chris Hani Baragwanath Hospital, Johannesburg, South Africa.
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