Continued Treatment with Nintedanib in Patients with Progressive Pulmonary Fibrosis: Data from INBUILD-ON

被引:0
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作者
Wuyts, Wim A. [1 ]
Bonella, Francesco [2 ]
Chaudhuri, Nazia [3 ]
Varone, Francesco [4 ]
Antin-Ozerkis, Danielle [5 ]
Song, Jin Woo [6 ]
Miede, Corinna [7 ]
Dumistracel, Mihaela [8 ]
Coeck, Carl [9 ]
Cottin, Vincent [10 ]
机构
[1] Univ Hosp Leuven, Dept Pulm Med, Unit Interstitial Lung Dis, Leuven, Belgium
[2] Univ Hosp Essen, Ctr Interstitial & Rare Lung Dis, Ruhrlandklin, Pneumol Dept, Essen, Germany
[3] Ulster Univ, Sch Med, Dept Life & Hlth Sci, Coleraine, North Ireland
[4] Fdn Policlin A Gemelli IRCCS, Rome, Italy
[5] Yale Univ, Sch Med, New Haven, CT USA
[6] Univ Ulsan, Coll Med, Asan Med Ctr, Seoul, South Korea
[7] Mainanalytics GmbH, Sulzbach, Germany
[8] Boehringer Ingelheim Pharm GmbH & Co KG, Ingelheim, Germany
[9] Boehringer Ingelheim SComm, Brussels, Belgium
[10] Claude Bernard Univ Lyon 1, Hosp Civils Lyon, Louis Pradel Hosp,ERN LUNG, Natl Reference Ctr Rare Pulm Dis,UMR 754, F-69677 Lyon, France
关键词
Clinical trial; Interstitial lung disease; Vital capacity; Pulmonary function tests; Drug tolerance;
D O I
10.1007/s00408-024-00778-z
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
PurposeIn the INBUILD trial in patients with progressive pulmonary fibrosis (PPF), nintedanib slowed the decline in forced vital capacity (FVC) versus placebo, with a safety profile characterised mainly by gastrointestinal events. INBUILD-ON, the open-label extension of INBUILD, assessed the safety of nintedanib during longer-term treatment. Data on FVC were collected.Study Design and MethodsAdverse events and changes in FVC in INBUILD-ON were assessed descriptively in all patients and in two subgroups: patients who received nintedanib in INBUILD and continued nintedanib in INBUILD-ON ("continued nintedanib" group) (n = 212) and patients who received placebo in INBUILD and initiated nintedanib in INBUILD-ON ("initiated nintedanib" group) (n = 222). Changes in FVC were based on observed values.ResultsMedian exposure to nintedanib in INBUILD-ON was 22.0 months. Diarrhoea was the most frequent adverse event. Amongst patients who had diarrhoea, 90.0% experienced only events of mild or moderate severity. Adverse events led to discontinuation of nintedanib at a rate of 16.7 per 100 patient-years. Serious and fatal adverse events were reported at rates of 37.2 and 9.5 per 100 patient-years. Mean (SE) changes in FVC from baseline to week 48 were - 71.6 (16.1) mL [- 128.5 (25.5) mL in continued nintedanib group (n = 106), - 14.8 (18.2) mL in initiated nintedanib group (n = 106)].ConclusionThe safety profile of nintedanib in INBUILD-ON was consistent with that in INBUILD. Change in FVC in INBUILD-ON was consistent with decline in FVC in the nintedanib group of INBUILD. These results support the use of nintedanib in the long-term treatment of PPF.Clinical Trial Registration: ClinicalTrials.gov; NCT03820726; registered January 29, 2019.ConclusionThe safety profile of nintedanib in INBUILD-ON was consistent with that in INBUILD. Change in FVC in INBUILD-ON was consistent with decline in FVC in the nintedanib group of INBUILD. These results support the use of nintedanib in the long-term treatment of PPF.Clinical Trial Registration: ClinicalTrials.gov; NCT03820726; registered January 29, 2019.
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页数:9
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