A Retrospective Analysis of Outcome in Melanoma Differentiation-Associated Gene 5-Related Interstitial Lung Disease Treated with Tofacitinib or Tacrolimus

被引:28
|
作者
Fan, Li [1 ]
Lyu, Wenting [1 ]
Liu, Huarui [1 ]
Jiang, Hanyi [1 ]
Chen, Lulu [1 ]
Liu, Yin [1 ]
Zhuang, Yi [1 ]
Huang, Mei [1 ]
Cao, Min [1 ]
Cai, Hourong [1 ]
Xiao, Yonglong [1 ,2 ]
Dai, Jinghong [1 ,2 ]
机构
[1] Jiangsu Univ, Nanjing Drum Tower Hosp, Clin Coll, Dept Pulm & Crit Care Med, Nanjing, Jiangsu, Peoples R China
[2] Jiangsu Univ, Nanjing Drum Tower Hosp, Clin Coll, Dept Pulm & Crit Care Med, Nanjing 210008, Peoples R China
基金
中国国家自然科学基金;
关键词
interstitial lung disease; MDA5; survival; tofacitinib; DERMATOMYOSITIS; CLASSIFICATION; SURVIVAL; ADULT;
D O I
10.3899/jrheum.220367
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective. The efficacy of tofacitinib (TOF) in the early diagnosis of melanoma differentiation-associated gene 5 (MDA5)-related interstitial lung disease (ILD) has been described. However, whether TOF exposure is associated with a reduced 1-year mortality rate remains undetermined.Methods. Patients diagnosed with MDA5-ILD receiving TOF or tacrolimus (TAC) treatment were included. A Cox proportional hazards model, which was adjusted for age, sex, smoking history, anti-MDA5 antibody titers, and concurrent use of other steroid-sparing agents, was performed to compare all-cause mor-tality and to investigate the risk factors predicting 1-year mortality rates in the 2 treatment groups.Results. During the study period, 26 patients were treated with TOF and 35 were treated with TAC. The 6-month (38.5% vs 62.9%; P = 0.03) and 1-year (44.0% vs 65.7%; P = 0.03) mortality rates in the TOF group were significantly lower than those in the TAC group. There were 13 patients diagnosed with rapidly progressive ILD (RP-ILD) in the TOF group and 22 in the TAC group. The majority of deaths occurred in patients with RP-ILD. The 6-month (76.9% vs 95.5%; P = 0.02) and 1-year (84.6% vs 100.0%; P = 0.02) mortality rates of patients with RP-ILD in the TOF group were also lower than those in the TAC group, respectively. The adjusted model showed that TOF exposure was associated with a lower risk for 1-year mor-tality (hazard ratio 0.44, 95% CI 0.20-0.96; P = 0.04). However, the incidence of adverse events (73.1% vs 74.3%; P > 0.99) and medication discontinuation rates (23.1% vs 14.3%; P = 0.50) in the TOF and TAC groups were similar, respectively. Conclusion. Our observational study showed that TOF use might have a potential effect on improving the outcomes of MDA5-ILD. Future clinical trials are needed to assess the long-term efficacy and tolerability of TOF.
引用
收藏
页码:1356 / 1364
页数:9
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