Nintedanib in chronic fibrosing interstitial lung diseases. A case series

被引:0
|
作者
Sevila, Raquel Garcia [1 ,4 ]
Jimenez, Juan Jose Arenas [2 ]
Casasempere, Paloma Vela [3 ]
Perez, Ester Nofuentes [1 ]
Garcia-Manso, Ignacio Gaya [1 ]
机构
[1] Dr Balmis Gen Univ Hosp, Pneumol Dept, ISABIAL, Alicante, Spain
[2] Dr Balmis Gen Univ Hosp, Radiol Dept, ISABIAL, Alicante, Spain
[3] Dr Balmis Gen Univ Hosp, Rheumatol Dept, ISABIAL, Alicante, Spain
[4] Hosp Gen Univ Alicante, Pneumol Dept, Pintor Baeza 12, Alicante 03010, Spain
关键词
Non -idiopathic interstitial lung diseases; Progressive pulmonary fibrosis; Antifibrotic therapy; Nintedanib; IDIOPATHIC PULMONARY-FIBROSIS;
D O I
10.1016/j.heliyon.2024.e28403
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Progressive pulmonary fibrosis (PPF) can be fatal in non-idiopathic interstitial lung diseases. We report a descriptive series of 13 patients with PPF who received treatment with nintedanib, a multitargeted tyrosine kinase inhibitor with antifibrotic effect. Although the reduced number of patients and the observational nature of a case series prevent us from providing strong evidence, our results suggest that nintedanib could be effective in PPF of various etiologies. Nintedanib could also be useful in specific populations such as patients awaiting lung transplant and elderly patients.
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页数:6
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