Effects of nintedanib in patients with idiopathic pulmonary fibrosis by GAP stage

被引:22
作者
Ryerson, Christopher J. [1 ,2 ]
Kolb, Martin [3 ]
Richeldi, Luca [4 ]
Lee, Joyce [5 ]
Wachtlin, Daniel [6 ]
Stowasser, Susanne [6 ]
Poletti, Venerino [7 ]
机构
[1] Univ British Columbia, Dept Med, Vancouver, BC, Canada
[2] Univ British Columbia, Ctr Heart Lung Innovat, Vancouver, BC, Canada
[3] McMaster Univ, Dept Med, Hamilton, ON, Canada
[4] Univ Cattolica Sacro Cuore, Fdn Policlin A Gemelli IRCCS, Rome, Italy
[5] Univ Colorado Denver, Dept Med, Aurora, CO USA
[6] Boehringer Ingelheim Int GmbH, Ingelheim, Germany
[7] Aarhus Univ Hosp, Dept Med, Aarhus, Denmark
关键词
FORCED VITAL CAPACITY; ACUTE EXACERBATION; EFFICACY; STANDARDIZATION; SUBGROUPS; MORTALITY; DECLINE; SAFETY; 1ST;
D O I
10.1183/23120541.00127-2018
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
We conducted a post hoc analysis to assess the potential impact of GAP (gender, age, physiology) stage on the treatment effect of nintedanib in patients with idiopathic pulmonary fibrosis. Outcomes were compared in patients at GAP stage I versus II/III at baseline in the INPULSIS (R) trials. At baseline, 500 patients were at GAP stage I (nintedanib 304, placebo 196), 489 were at GAP stage II (nintedanib 296, placebo 193) and 71 were at GAP stage III (nintedanib 38, placebo 33). In nintedanib-treated patients, the annual rate of decline in forced vital capacity (FVC) was similar in patients at GAP stage I and GAP stage II/III at baseline (-110.1 and -116.6 mL.year(-1), respectively), and in both subgroups was lower than in placebo-treated patients (-218.5 and -227.6 mL.year(-1), respectively) (treatment-by-time-by-subgroup interaction p=0.92). In the nintedanib group, the number of deaths was 43.8% of those predicted based on GAP stage (35 versus 79.9). In the placebo group, the number of deaths was 59.8% of those predicted based on GAP stage (33 versus 55.2). In conclusion, data from the INPULSIS (R) trials suggest that nintedanib has a similar beneficial effect on the rate of FVC decline in patients at GAP stage I versus II/III at baseline.
引用
收藏
页数:9
相关论文
共 24 条
[1]   Acute exacerbations in the INPULSIS trials of nintedanib in idiopathic pulmonary fibrosis [J].
Collard, Harold R. ;
Richeldi, Luca ;
Kim, Dong Soon ;
Taniguchi, Hiroyuki ;
Tschoepe, Inga ;
Luisetti, Maurizio ;
Roman, Jesse ;
Tino, Gregory ;
Schlenker-Herceg, Rozsa ;
Hallmann, Christoph ;
du Bois, Roland M. .
EUROPEAN RESPIRATORY JOURNAL, 2017, 49 (05)
[2]   Acute Exacerbation of Idiopathic Pulmonary Fibrosis An International Working Group Report [J].
Collard, Harold R. ;
Ryerson, Christopher J. ;
Corte, Tamera J. ;
Jenkins, Gisli ;
Kondoh, Yasuhiro ;
Lederer, David J. ;
Lee, Joyce S. ;
Maher, Toby M. ;
Wells, Athol U. ;
Antoniou, Katerina M. ;
Behr, Juergen ;
Brown, Kevin K. ;
Cottin, Vincent ;
Flaherty, Kevin R. ;
Fukuoka, Junya ;
Hansell, David M. ;
Johkoh, Takeshi ;
Kaminski, Naftali ;
Kim, Dong Soon ;
Kolb, Martin ;
Lynch, David A. ;
Myers, Jeffrey L. ;
Raghu, Ganesh ;
Richeldi, Luca ;
Taniguchi, Hiroyuki ;
Martinez, Fernando J. .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2016, 194 (03) :265-275
[3]   Efficacy of Nintedanib in Idiopathic Pulmonary Fibrosis across Prespecified Subgroups in INPULSIS [J].
Costabel, Ulrich ;
Inoue, Yoshikazu ;
Richeldi, Luca ;
Collard, Harold R. ;
Tschoepe, Inga ;
Stowasser, Susanne ;
Azuma, Arata .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2016, 193 (02) :178-185
[4]   Forced Vital Capacity in Patients with Idiopathic Pulmonary Fibrosis Test Properties and Minimal Clinically Important Difference [J].
du Bois, Roland M. ;
Weycker, Derek ;
Albera, Carlo ;
Bradford, Williamson Z. ;
Costabel, Ulrich ;
Kartashov, Alex ;
King, Talmadge E., Jr. ;
Lancaster, Lisa ;
Noble, Paul W. ;
Sahn, Steven A. ;
Thomeer, Michiel ;
Valeyre, Dominique ;
Wells, Athol U. .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2011, 184 (12) :1382-1389
[5]   THE ST-GEORGE RESPIRATORY QUESTIONNAIRE [J].
JONES, PW ;
QUIRK, FH ;
BAVEYSTOCK, CM .
RESPIRATORY MEDICINE, 1991, 85 :25-31
[6]   Nintedanib in patients with idiopathic pulmonary fibrosis and preserved lung volume [J].
Kolb, Martin ;
Richeldi, Luca ;
Behr, Juergen ;
Maher, Toby M. ;
Tang, Wenbo ;
Stowasser, Susanne ;
Hallmann, Christoph ;
du Bois, Roland M. .
THORAX, 2017, 72 (04) :340-346
[7]   Predictors of Mortality Poorly Predict Common Measures of Disease Progression in Idiopathic Pulmonary Fibrosis [J].
Ley, Brett ;
Bradford, Williamson Z. ;
Vittinghoff, Eric ;
Weycker, Derek ;
du Bois, Roland M. ;
Collard, Harold R. .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2016, 194 (06) :711-718
[8]   A Multidimensional Index and Staging System for Idiopathic Pulmonary Fibrosis [J].
Ley, Brett ;
Ryerson, Christopher J. ;
Vittinghoff, Eric ;
Ryu, Jay H. ;
Tomassetti, Sara ;
Lee, Joyce S. ;
Poletti, Venerino ;
Buccioli, Matteo ;
Elicker, Brett M. ;
Jones, Kirk D. ;
King, Talmadge E., Jr. ;
Collard, Harold R. .
ANNALS OF INTERNAL MEDICINE, 2012, 156 (10) :684-U58
[9]   Clinical Course and Prediction of Survival in Idiopathic Pulmonary Fibrosis [J].
Ley, Brett ;
Collard, Harold R. ;
King, Talmadge E., Jr. .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2011, 183 (04) :431-440
[10]   Standardisation of the single-breath determination of carbon monoxide uptake in the lung [J].
MacIntyre, N ;
Crapo, RO ;
Viegi, G ;
Johnson, DC ;
van der Grinten, CPM ;
Brusasco, V ;
Burgos, F ;
Casaburi, R ;
Coates, A ;
Enright, P ;
Gustafsson, P ;
Hankinson, J ;
Jensen, R ;
McKay, R ;
Miller, MR ;
Navajas, D ;
Pedersen, OF ;
Pellegrino, R ;
Wanger, J .
EUROPEAN RESPIRATORY JOURNAL, 2005, 26 (04) :720-735