Nintedanib plus Sildenafil in Patients with Idiopathic Pulmonary Fibrosis

被引:200
作者
Kolb, Martin [1 ,2 ]
Raghu, Ganesh [3 ]
Wells, Athol U. [4 ,5 ]
Behr, Juergen [6 ,7 ]
Richeldi, Luca [9 ]
Schinzel, Birgit [8 ]
Quaresma, Manuel [8 ]
Stowasser, Susanne [8 ]
Martinez, Fernando J. [10 ]
机构
[1] McMaster Univ, Hamilton, ON, Canada
[2] St Josephs Healthcare, Hamilton, ON, Canada
[3] Univ Washington, Seattle, WA 98195 USA
[4] Royal Brompton & Harefield NHS Fdn Trust, Natl Inst Hlth Res Resp Biomed Res Unit, London, England
[5] Imperial Coll, Natl Heart & Lung Inst, London, England
[6] Univ Munich, Med Klin & Poliklin 5, Munich, Germany
[7] German Ctr Lung Res, Asklepios Klin Munchen Gauting, Munich, Germany
[8] Boehringer Ingelheim Int, Ingelheim, Germany
[9] Univ Cattolica Sacro Cuore, Fdn Policlin A Gemelli IRCCS, Rome, Italy
[10] Weill Cornell Med, New York, NY USA
关键词
BREATH QUESTIONNAIRE; CONTROLLED-TRIAL; UCSD SHORTNESS; HYPERTENSION; EFFICACY; GUIDELINES; DIAGNOSIS;
D O I
10.1056/NEJMoa1811737
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND Nintedanib is an approved treatment for idiopathic pulmonary fibrosis (IPF). A subgroup analysis of a previously published trial suggested that sildenafil may provide benefits regarding oxygenation, gas exchange as measured by the diffusion capacity of the lungs for carbon monoxide (DLCO), symptoms, and quality of life in patients with IPF and severely decreased DLCO. That idea was tested in this trial. METHODS We randomly assigned, in a 1: 1 ratio, patients with IPF and a DLCO of 35% or less of the predicted value to receive nintedanib at a dose of 150 mg twice daily plus sildenafil at a dose of 20 mg three times daily (nintedanib-plus-sildenafil group) or nintedanib at a dose of 150 mg twice daily plus placebo three times daily (nintedanib group) for 24 weeks. The primary end point was the change from baseline in the total score on the St. George's Respiratory Questionnaire (SGRQ) at week 12 (the total score ranges from 0 to 100, with higher scores indicating worse health-related quality of life). Secondary end points included measures of dyspnea and safety. RESULTS A total of 274 patients underwent randomization. There was no significant difference in the adjusted mean change from baseline in the SGRQ total score at week 12 between the nintedanib-plus-sildenafil group and the nintedanib group (-1.28 points and -0.77 points, respectively; P = 0.72). A benefit from sildenafil treatment was not observed with regard to dyspnea as measured with the use of the University of California, San Diego, Shortness of Breath Questionnaire. No new safety signals were observed, as compared with previous trials. CONCLUSIONS In patients with IPF and a DLCO of 35% or less of the predicted value, nintedanib plus sildenafil did not provide a significant benefit as compared with nintedanib alone. No new safety signals were identified with either treatment regimen in this population of patients. (Funded by Boehringer Ingelheim; INSTAGE ClinicalTrials.gov number, NCT02802345.)
引用
收藏
页码:1722 / 1731
页数:10
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