Efficacy of Pirfenidone in the Context of Multiple Disease Progression Events in Patients With Idiopathic Pulmonary Fibrosis

被引:30
作者
Nathan, Steven D. [1 ]
Costabel, Ulrich [2 ]
Glaspole, Ian [3 ,4 ]
Glassberg, Marilyn K. [5 ]
Lancaster, Lisa H. [6 ]
Lederer, David J. [7 ,8 ]
Pereira, Carlos A. [9 ]
Trzaskoma, Benjamin [10 ]
Morgenthien, Elizabeth A. [10 ]
Limb, Susan L. [10 ]
Wells, Athol U. [11 ]
机构
[1] Inova Fairfax Hosp, Adv Lung Dis & Transplant Program, 3300 Gallows Rd, Falls Church, VA 22042 USA
[2] Univ Hosp, Univ Duisburg Essen, Ruhrland Klin, Interstitial & Rare Lung Dis Unit, Essen, Germany
[3] Alfred Hosp, Dept Allergy Immunol & Resp Med, Melbourne, Vic, Australia
[4] Monash Univ, Melbourne, Vic, Australia
[5] Univ Miami, Miller Sch Med, Dept Med, Miami, FL 33136 USA
[6] Vanderbilt Univ, Med Ctr, Div Allergy Pulm & Crit Care Med, Nashville, TN USA
[7] Columbia Univ, Med Ctr, Dept Med, New York, NY USA
[8] Columbia Univ, Med Ctr, Dept Epidemiol, New York, NY USA
[9] Univ Fed Sao Paulo, Paulista Sch Med, Lung Dis Dept, Sao Paulo, Brazil
[10] Genentech Inc, San Francisco, CA 94080 USA
[11] Royal Brompton Hosp, London, England
关键词
disease progression; idiopathic pulmonary fibrosis; interstitial lung diseases; pirfenidone; FORCED VITAL CAPACITY; MORTALITY; SURVIVAL; TRIALS;
D O I
10.1016/j.chest.2018.11.008
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
BACKGROUND: Declines in percent predicted FVC (% predicted FVC), declines in 6-min walk distance (6MWD), and respiratory hospitalizations are events associated with disease progression and mortality in idiopathic pulmonary fibrosis. The incidence of multiple events in the same patient over 12 months of pirfenidone treatment is unknown. METHODS: Patients who received pirfenidone 2,403 mg/d (n = 623) or placebo (n = 624) in the ASCEND (study 016; NCT01366209) and CAPACITY (studies 004 and 006; NCT00287716 and NCT00287729) phase III trials were included in this post hoc analysis. Disease progression events were defined as relative decline in % predicted FVC $ 10%, absolute decline in 6MWD $ 50 m, respiratory hospitalization, or death from any cause. The incidence of disease progression events over 12 months was assessed. RESULTS: The most frequent disease progression events were declines in % predicted FVC (pirfenidone vs placebo; 202 vs 304 events) and declines in 6MWD (pirfenidone vs placebo; 265 vs 348 events). Fewer patients who received pirfenidone had more than one progression event compared with placebo (17.0% vs 30.1%; P <.0001). Death following one or more progression event occurred less frequently in the pirfenidone group than in the placebo group (2.1% vs 6.3%; P = .0002). CONCLUSIONS: Pirfenidone significantly reduced the incidence of multiple progression events and death after a progression event over 12 months of treatment compared with placebo. These findings suggest that continued treatment with pirfenidone confers a benefit despite the occurrence of any single disease progression event.
引用
收藏
页码:712 / 719
页数:8
相关论文
共 17 条
  • [1] Forced Vital Capacity in Patients with Idiopathic Pulmonary Fibrosis Test Properties and Minimal Clinically Important Difference
    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.
    [J]. AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2011, 184 (12) : 1382 - 1389
  • [2] du Bois RM, 2011, AM J RESP CRIT CARE, V183, P1231, DOI [10.1164/rccm.201007.1179OC, 10.1164/rccm.201007-1179OC]
  • [3] Association of hospital admission and forced vital capacity endpoints with survival in patients with idiopathic pulmonary fibrosis: analysis of a pooled cohort from three clinical trials
    Durheim, Michael T.
    Collard, Harold R.
    Roberts, Rhonda S.
    Brown, Kevin K.
    Flaherty, Kevin R.
    King, Talmadge E., Jr.
    Palmer, Scott M.
    Raghu, Ganesh
    Snyder, Laurie D.
    Anstrom, Kevin J.
    Martinez, Fernando J.
    [J]. LANCET RESPIRATORY MEDICINE, 2015, 3 (05) : 388 - 396
  • [4] A Phase 3 Trial of Pirfenidone in Patients with Idiopathic Pulmonary Fibrosis
    King, Talmadge E., Jr.
    Bradford, Williamson Z.
    Castro-Bernardini, Socorro
    Fagan, Elizabeth A.
    Glaspole, Ian
    Glassberg, Marilyn K.
    Gorina, Eduard
    Hopkins, Peter M.
    Kardatzke, David
    Lancaster, Lisa
    Lederer, David J.
    Nathan, Steven D.
    Pereira, Carlos A.
    Sahn, Steven A.
    Sussman, Robert
    Swigris, Jeffrey J.
    Noble, Paul W.
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2014, 370 (22) : 2083 - 2092
  • [5] Pirfenidone Reduces Respiratory-related Hospitalizations in Idiopathic Pulmonary Fibrosis
    Ley, Brett
    Swigris, Jeffrey
    Day, Bann-mo
    Stauffer, John L.
    Raimundo, Karina
    Chou, Willis
    Collard, Harold R.
    [J]. AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2017, 196 (06) : 756 - 761
  • [6] Clinical Course and Prediction of Survival in Idiopathic Pulmonary Fibrosis
    Ley, Brett
    Collard, Harold R.
    King, Talmadge E., Jr.
    [J]. AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2011, 183 (04) : 431 - 440
  • [7] Effect of continued pirfenidone treatment following a ≥ 15% decline in 6-minute walk distance (6MWD) in patients with idiopathic pulmonary fibrosis (IPF): Pooled analysis from 3 pivotal studies
    Nathan, Steven
    Albera, Carlo
    Costabel, Ulrich
    Glaspole, Ian
    Glassberg, Marilyn
    Lancaster, Lisa
    Lederer, David
    Pereira, Carlos
    Swigris, Jeffrey
    Pavlov, Andrey
    Stauffer, John
    Day, Bann-Mo
    Chou, Willis
    Wells, Athol
    [J]. EUROPEAN RESPIRATORY JOURNAL, 2016, 48
  • [8] Effect of pirfenidone on mortality: pooled analyses and meta-analyses of clinical trials in idiopathic pulmonary fibrosis
    Nathan, Steven D.
    Albera, Carlo
    Bradford, Williamson Z.
    Costabel, Ulrich
    Glaspole, Ian
    Glassberg, Marilyn K.
    Kardatzke, David R.
    Daigl, Monica
    Kirchgaessler, Klaus-Uwe
    Lancaster, Lisa H.
    Lederer, David J.
    Pereira, Carlos A.
    Swigris, Jeffrey J.
    Valeyre, Dominique
    Noble, Paul W.
    [J]. LANCET RESPIRATORY MEDICINE, 2017, 5 (01) : 33 - 41
  • [9] Effect of continued treatment with pirfenidone following clinically meaningful declines in forced vital capacity: analysis of data from three phase 3 trials in patients with idiopathic pulmonary fibrosis
    Nathan, Steven D.
    Albera, Carlo
    Bradford, Williamson Z.
    Costabel, Ulrich
    du Bois, Roland M.
    Fagan, Elizabeth A.
    Fishman, Robert S.
    Glaspole, Ian
    Glassberg, Marilyn K.
    Glasscock, Kenneth F.
    King, Talmadge E., Jr.
    Lancaster, Lisa
    Lederer, David J.
    Lin, Zhengning
    Pereira, Carlos A.
    Swigris, Jeffrey J.
    Valeyre, Dominique
    Noble, Paul W.
    Wells, Athol U.
    [J]. THORAX, 2016, 71 (05) : 429 - 435
  • [10] Pirfenidone for idiopathic pulmonary fibrosis: analysis of pooled data from three multinational phase 3 trials
    Noble, Paul W.
    Albera, Carlo
    Bradford, Williamson Z.
    Costabel, Ulrich
    du Bois, Roland M.
    Fagan, Elizabeth A.
    Fishman, Robert S.
    Glaspole, Ian
    Glassberg, Marilyn K.
    Lancaster, Lisa
    Lederer, David J.
    Leff, Jonathan A.
    Nathan, Steven D.
    Pereira, Carlos A.
    Swigris, Jeffrey J.
    Valeyre, Dominique
    King, Talmadge E., Jr.
    [J]. EUROPEAN RESPIRATORY JOURNAL, 2016, 47 (01) : 243 - 253