The effect of Rituximab treatment on progression of Rheumatoid arthritis-associated interstitial lung disease

Sukhmani Sra, K. Myall, B. Lams, S. Agarwal, A. West
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引用次数: 2

Abstract

Introduction: Interstitial lung disease (ILD) commonly occurs in the context of Rheumatoid arthritis (RA), and is associated with significant morbidity and mortality. Rituximab is commonly used in the treatment of articular Rheumatoid arthritis and has been shown to be safe in patients with ILD. Aims and objectives: We aimed to study the effect of Rituximab treatment on the progression of RA-ILD as measured by decline in FVC and TLCO. Methods: A retrospective analysis of patients with RA treated at a tertiary referral centre in the United Kingdom between November 2016 and November 2018 was performed. Patients with at least 3 months’ follow up were included if they had at least two lung function tests performed. Decline was measured either from first administration of Rituximab or from first available lung function (no treatment group). Results: 44 patients were identified who met the study criteria. Patients had follow up of a median 23.5 (range 6-89) months. In the group treated with Rituximab, 9 of 26 patients (34.6%) progressed (defined by a decline in FVC of > 10% or TLCO of > 15% or death due to respiratory disease) at a median of 23 months (range 8-44). In the group that did not receive Rituximab, 11 of 18 patients (61.1%) had progression of disease at a median of 18 months (range 3-44). There was a trend towards significance (p=0.08) in rate of decline in FVC between the two groups favouring Rituximab. Conclusions: In patients with RA-ILD, Rituximab was associated with a slower rate of progression when measured by decline in lung function. This supports the use of Rituximab in the management RA-ILD and the development of robust trials.
利妥昔单抗治疗对类风湿关节炎相关间质性肺疾病进展的影响
间质性肺疾病(ILD)通常发生在类风湿关节炎(RA)的背景下,并与显著的发病率和死亡率相关。利妥昔单抗通常用于治疗关节类风湿性关节炎,并已被证明对ILD患者是安全的。目的和目的:我们旨在通过FVC和TLCO的下降来研究利妥昔单抗治疗对RA-ILD进展的影响。方法:回顾性分析2016年11月至2018年11月期间在英国三级转诊中心治疗的RA患者。随访至少3个月的患者,如果他们进行了至少两次肺功能检查。从首次给药利妥昔单抗或首次可用肺功能(无治疗组)测量下降。结果:44例患者符合研究标准。患者的中位随访时间为23.5个月(6-89个月)。在接受利妥昔单抗治疗的组中,26例患者中有9例(34.6%)进展(定义为FVC下降> 10%或TLCO > 15%或因呼吸系统疾病死亡),中位时间为23个月(范围8-44)。在未接受利妥昔单抗治疗的组中,18名患者中有11名(61.1%)在中位18个月(范围3-44个月)出现疾病进展。利妥昔单抗治疗组与对照组间FVC下降率有显著性差异(p=0.08)。结论:在RA-ILD患者中,通过肺功能下降来测量,利妥昔单抗与较慢的进展速度相关。这支持了利妥昔单抗在RA-ILD治疗中的应用,并开展了强有力的临床试验。
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