Robles-Perez Alejandro, Dorca Jordi, Castellví Ivan, Nolla Joan Miquel, Molina-Molina Maria, Narváez Javier
ILD Unit, Pneumology Department, Hospital Universitari de Bellvitge, Barcelona, Spain.
Pneumology Department, Hospital Universitari de Bellvitge, Feixa Llarga S/N, 08907, Barcelona, Spain.
Rheumatol Int. 2020 May;40(5):719-726. doi: 10.1007/s00296-020-04545-0. Epub 2020 Mar 10.
Progressive connective tissue disease (CTD)-related lung disease is a challenging condition that requires lung transplantation in some patients. Treatment with rituximab may improve lung function. To evaluate the effect of rituximab in patients with progressive CTD-related lung disease who met criteria for inclusion in waiting list for a lung transplant. Retrospective study of patients with progressive CTD-related lung disease with criteria for lung transplant (FVC < 60% and/or DLCO < 40%) that started treatment with rituximab because of disease progression. Clinical variables, pulmonary function tests and chest computed tomography were used to monitor the effect of rituximab. The cohort included 18 patients; systemic sclerosis (7), rheumatoid arthritis (5), systemic lupus erythematosus (4), Sjögren syndrome (1) and antisynthetase syndrome (1). The radiologic patterns observed were: usual interstitial pneumonia (1), non-specific interstitial pneumonia (9), lymphoid interstitial pneumonia (1), emphysema-usual interstitial pneumonia (1), shrinking lung syndrome (3) and undetermined pattern (3). Over the previous year to rituximab initiation a decline in FVC (- 3.8%, p = 0.095) and DLCO (- 8.4%, p = 0.004) was observed. After 2 years of treatment, DLCO significantly improved (+ 12.4%, p < 0.001 at 1 year and + 15.3%, p = 0.001 at 2 years). Six patients (33.3%) presented adverse events related to rituximab. No patient required lung transplant or died during the study period. Rituximab is an effective treatment for patients with severe and progressive CTD-related lung disease, which allows to delay lung transplantation in some cases.
进行性结缔组织病(CTD)相关的肺部疾病是一种具有挑战性的病症,部分患者需要进行肺移植。利妥昔单抗治疗可能会改善肺功能。本研究旨在评估利妥昔单抗对符合肺移植等待名单纳入标准的进行性CTD相关肺部疾病患者的疗效。对因疾病进展而开始接受利妥昔单抗治疗、符合肺移植标准(用力肺活量[FVC]<60%和/或一氧化碳弥散量[DLCO]<40%)的进行性CTD相关肺部疾病患者进行回顾性研究。采用临床变量、肺功能测试和胸部计算机断层扫描来监测利妥昔单抗的疗效。该队列包括18例患者;系统性硬化症(7例)、类风湿关节炎(5例)、系统性红斑狼疮(4例)、干燥综合征(1例)和抗合成酶综合征(1例)。观察到的放射学模式有:普通间质性肺炎(1例)、非特异性间质性肺炎(9例)、淋巴细胞间质性肺炎(1例)、肺气肿-普通间质性肺炎(1例)、肺萎陷综合征(3例)和未确定模式(3例)。在开始使用利妥昔单抗的前一年,观察到FVC下降(-3.8%,p=0.095)和DLCO下降(-8.4%,p=0.004)。治疗2年后,DLCO显著改善(1年时增加12.4%,p<0.001;2年时增加15.3%,p=0.001)。6例患者(33.3%)出现与利妥昔单抗相关的不良事件。在研究期间,没有患者需要进行肺移植或死亡。利妥昔单抗是治疗严重进行性CTD相关肺部疾病患者的有效药物,在某些情况下可延迟肺移植。