Seedat U F, Christian B, Boshoff P E, Gaylard P, Schleicher G K
Wits Donald Gordon Medical Centre, University of the Witwatersrand, Johannesburg, South Africa.
DGMC Radiology, Wits Donald Gordon Medical Centre, University of the Witwatersrand, Johannesburg, South Africa.
Afr J Thorac Crit Care Med. 2024 Oct 14;30(3):e1431. doi: 10.7196/AJTCCM.2024.v30i3.1431. eCollection 2024.
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.
To investigate the therapeutic effects and safety of RTX in patients with severe CTD-ILD.
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.
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.
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.
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. This small study suggests a possible role for RTX therapy in severe or refractory CTD-ILD.
尽管采用一线免疫抑制治疗,结缔组织病相关间质性肺病(CTD-ILD)仍进展,这是一个临床挑战。利妥昔单抗(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,已被用作重症疾病的挽救治疗方式。
研究RTX对重症CTD-ILD患者的治疗效果和安全性。
对2010年1月至2020年12月期间在南非约翰内斯堡威特斯唐纳德·戈登医疗中心接受挽救性RTX治疗及各种免疫调节治疗组合的重症CTD-ILD患者进行回顾性观察分析。共分析了19例病情进展的CTD-ILD患者,这些患者有足够的数据且随访24个月。通过系列肺功能测试、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用挽救性RTX的效果。
从基线开始随访24个月时,开始RTX挽救治疗后用力肺活量无显著下降(0.01L;95%CI -0.13 - 0.14)(p=0.91)。系列胸部HRCT显示,19例患者中有13例(68%)影像学疾病稳定或改善。FC评估显示与基线相比无显著恶化(p=0.083)。未记录到严重药物不良反应或死亡。
挽救性RTX治疗联合各种免疫调节治疗,在24个月期间使大多数重症CTD-ILD患者病情稳定。
结缔组织病相关间质性肺病(CTD-ILD)是一个具有挑战性的临床实体。利妥昔单抗(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,已被建议作为难治性或重症疾病的潜在治疗方式。本文介绍了在进展性CTD-ILD中进行RTX挽救治疗的单中心经验。这项小型研究表明RTX治疗在重症或难治性CTD-ILD中可能发挥作用。