Real-world retrospective observational study exploring the effectiveness and safety of antifibrotics in idiopathic pulmonary fibrosis

被引:33
作者
Wright, William Alexander [1 ]
Crowley, Louise E. [2 ]
Parekh, Dhruv [2 ,3 ]
Crawshaw, Anjali [2 ]
Dosanjh, Davinder P. [2 ,3 ]
Nightingale, Peter [2 ]
Thickett, David R. [2 ,3 ]
机构
[1] Univ Birmingham, Sch Med & Dent Sci, Inst Inflammat & Ageing, Birmingham, W Midlands, England
[2] Univ Hosp Birmingham NHS Fdn Trust, Dept Resp Med, Birmingham, W Midlands, England
[3] Univ Birmingham, Inst Inflammat & Ageing, Birmingham, W Midlands, England
基金
英国医学研究理事会;
关键词
interstitial fibrosis;
D O I
10.1136/bmjresp-2020-000782
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Background Pirfenidone and nintedanib are the only disease-modifying treatments available for idiopathic pulmonary fibrosis (IPF). Our aim was to test their effectiveness and safety in clinical practice. Methods This is a single-centre retrospective observational study undertaken at a specialised interstitial lung disease centre in England. Data including progression-free survival (PFS), mortality and drug tolerability were compared between patients with IPF on antifibrotic therapies and an untreated control group who had a forced vital capacity percentage (FVC %) predicted within the licensed antifibrotic treatment range. Results 104 patients received antifibrotic therapies and 64 control patients were identified. PFS at 6 months was significantly greater in the antifibrotic group (75.0%) compared with the control group (56.3%) (p=0.012). PFS was not significant at 12 or 18 months when comparing the antifibrotic group with the control group. The 12-month post-treatment mean decline in FVC % predicted (-4.6 +/- 6.2%) was significantly less than the 12-month pretreatment decline (-10.4 +/- 11.8%) (p=0.039). The 12-month mortality rate was not significantly different between the antifibrotic group (25.3%) and the control group (35.5%) (p=0.132). Baseline Body Mass Index of <= 25, baseline diffusion capacity for carbon monoxide percentage predicted of <= 35 and antifibrotic discontinuation within 3 months were independent predictors of 12-month mortality. Antifibrotic discontinuation was significantly higher by 3 and 6 months for patients on pirfenidone than those on nintedanib (p=0.006 and p=0.044, respectively). Discontinuation at 12 months was not significantly different (p=0.381). Conclusions This real-world study revealed that antifibrotics are having promising effects on PFS, lung function and mortality. These findings may favour commencement of nintedanib as first-line antifibrotic therapy, given the lower rates of early treatment discontinuation, although further studies are required to investigate this.
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