메뉴 건너뛰기




Volumn 5, Issue 1, 2018, Pages

Investigating the effects of nintedanib on biomarkers of extracellular matrix turnover in patients with IPF: Design of the randomised placebo-controlled INMARK®trial

Author keywords

Interstitial fibrosis

Indexed keywords

ALANINE AMINOTRANSFERASE; ASPARTATE AMINOTRANSFERASE; BIOLOGICAL MARKER; NINTEDANIB; PLACEBO; VASCULOTROPIN;

EID: 85052670322     PISSN: None     EISSN: 20524439     Source Type: Journal    
DOI: 10.1136/bmjresp-2018-000325     Document Type: Article
Times cited : (14)

References (39)
  • 1
    • 79952717349 scopus 로고    scopus 로고
    • An official ATS/ERS/JRS/ALAT statement: Idiopathic pulmonary fibrosis: Evidence-based guidelines for diagnosis and management
    • Raghu G, Collard HR, Egan JJ, et al. An official ATS/ERS/JRS/ALAT statement: idiopathic pulmonary fibrosis: evidence-based guidelines for diagnosis and management. Am J Respir Crit Care Med 2011;183:788-824.
    • (2011) Am J Respir Crit Care Med , vol.183 , pp. 788-824
    • Raghu, G.1    Collard, H.R.2    Egan, J.J.3
  • 2
    • 84896767563 scopus 로고    scopus 로고
    • Predicting pulmonary fibrosis disease course from past trends in pulmonary function
    • Schmidt SL, Tayob N, Han MK, et al. Predicting pulmonary fibrosis disease course from past trends in pulmonary function. Chest 2014;145:579-85.
    • (2014) Chest , vol.145 , pp. 579-585
    • Schmidt, S.L.1    Tayob, N.2    Han, M.K.3
  • 3
    • 84988924204 scopus 로고    scopus 로고
    • Predictors of mortality poorly predict common measures of disease progression in idiopathic pulmonary fibrosis
    • Ley B, Bradford WZ, Vittinghoff E, et al. Predictors of mortality poorly predict common measures of disease progression in idiopathic pulmonary fibrosis. Am J Respir Crit Care Med 2016;194:711-8.
    • (2016) Am J Respir Crit Care Med , vol.194 , pp. 711-718
    • Ley, B.1    Bradford, W.Z.2    Vittinghoff, E.3
  • 4
    • 84878600828 scopus 로고    scopus 로고
    • Association between the MUC5B promoter polymorphism and survival in patients with idiopathic pulmonary fibrosis
    • Peljto AL, Zhang Y, Fingerlin TE, et al. Association between the MUC5B promoter polymorphism and survival in patients with idiopathic pulmonary fibrosis. JAMA 2013;309:2232-9.
    • (2013) JAMA , vol.309 , pp. 2232-2239
    • Peljto, A.L.1    Zhang, Y.2    Fingerlin, T.E.3
  • 5
    • 85029640399 scopus 로고    scopus 로고
    • Validation of a 52-gene risk profile for outcome prediction in patients with idiopathic pulmonary fibrosis: An international, multicentre, cohort study
    • Herazo-Maya JD, Sun J, Molyneaux PL, et al. Validation of a 52-gene risk profile for outcome prediction in patients with idiopathic pulmonary fibrosis: an international, multicentre, cohort study. Lancet Respir Med 2017;5:857-68.
    • (2017) Lancet Respir Med , vol.5 , pp. 857-868
    • Herazo-Maya, J.D.1    Sun, J.2    Molyneaux, P.L.3
  • 6
    • 0036196542 scopus 로고    scopus 로고
    • Serum surfactant proteins-A and-D as biomarkers in idiopathic pulmonary fibrosis
    • Greene KE, King TE, Kuroki Y, et al. Serum surfactant proteins-A and-D as biomarkers in idiopathic pulmonary fibrosis. Eur Respir J 2002;19:439-46.
    • (2002) Eur Respir J , vol.19 , pp. 439-446
    • Greene, K.E.1    King, T.E.2    Kuroki, Y.3
  • 7
    • 33644828168 scopus 로고    scopus 로고
    • Prognostic value of circulating KL-6 in idiopathic pulmonary fibrosis
    • Yokoyama A, Kondo K, Nakajima M, et al. Prognostic value of circulating KL-6 in idiopathic pulmonary fibrosis. Respirology 2006;11:164-8.
    • (2006) Respirology , vol.11 , pp. 164-168
    • Yokoyama, A.1    Kondo, K.2    Nakajima, M.3
  • 8
    • 43249084804 scopus 로고    scopus 로고
    • MMP1 and MMP7 as potential peripheral blood biomarkers in idiopathic pulmonary fibrosis
    • Rosas IO, Richards TJ, Konishi K, et al. MMP1 and MMP7 as potential peripheral blood biomarkers in idiopathic pulmonary fibrosis. PLoS Med 2008;5:e93.
    • (2008) PLoS Med , vol.5 , pp. e93
    • Rosas, I.O.1    Richards, T.J.2    Konishi, K.3
  • 9
    • 84855264195 scopus 로고    scopus 로고
    • Peripheral blood proteins predict mortality in idiopathic pulmonary fibrosis
    • Richards TJ, Kaminski N, Baribaud F, et al. Peripheral blood proteins predict mortality in idiopathic pulmonary fibrosis. Am J Respir Crit Care Med 2012;185:67-76.
    • (2012) Am J Respir Crit Care Med , vol.185 , pp. 67-76
    • Richards, T.J.1    Kaminski, N.2    Baribaud, F.3
  • 10
    • 85033779884 scopus 로고    scopus 로고
    • An epithelial biomarker signature for idiopathic pulmonary fibrosis: An analysis from the multicentre PROFILE cohort study
    • Maher TM, Oballa E, Simpson JK, et al. An epithelial biomarker signature for idiopathic pulmonary fibrosis: an analysis from the multicentre PROFILE cohort study. Lancet Respir Med 2017;5:946-55.
    • (2017) Lancet Respir Med , vol.5 , pp. 946-955
    • Maher, T.M.1    Oballa, E.2    Simpson, J.K.3
  • 11
    • 0024561372 scopus 로고
    • Hyaluronan and type III procollagen peptide concentrations in bronchoalveolar lavage fluid in idiopathic pulmonary fibrosis
    • Bjermer L, Lundgren R, Hallgren R. Hyaluronan and type III procollagen peptide concentrations in bronchoalveolar lavage fluid in idiopathic pulmonary fibrosis. Thorax 1989;44:126-31.
    • (1989) Thorax , vol.44 , pp. 126-131
    • Bjermer, L.1    Lundgren, R.2    Hallgren, R.3
  • 12
    • 84918777951 scopus 로고    scopus 로고
    • The role of bacteria in the pathogenesis and progression of idiopathic pulmonary fibrosis
    • Molyneaux PL, Cox MJ, Willis-Owen SA, et al. The role of bacteria in the pathogenesis and progression of idiopathic pulmonary fibrosis. Am J Respir Crit Care Med 2014;190:906-13.
    • (2014) Am J Respir Crit Care Med , vol.190 , pp. 906-913
    • Molyneaux, P.L.1    Cox, M.J.2    Willis-Owen, S.A.3
  • 13
    • 84903993583 scopus 로고    scopus 로고
    • Association between lung microbiome and disease progression in IPF: A prospective cohort study
    • Han MK, Zhou Y, Murray S, et al. Association between lung microbiome and disease progression in IPF: a prospective cohort study. Lancet Respir Med 2014;2:548-56.
    • (2014) Lancet Respir Med , vol.2 , pp. 548-556
    • Han, M.K.1    Zhou, Y.2    Murray, S.3
  • 14
    • 84992602716 scopus 로고    scopus 로고
    • Texture-based automated quantitative assessment of regional patterns on initial CT in patients with idiopathic pulmonary fibrosis: Relationship to decline in forced vital capacity
    • Park HJ, Lee SM, Song JW, et al. Texture-based automated quantitative assessment of regional patterns on initial CT in patients with idiopathic pulmonary fibrosis: relationship to decline in forced vital capacity. AJR Am J Roentgenol 2016;207:976-83.
    • (2016) AJR Am J Roentgenol , vol.207 , pp. 976-983
    • Park, H.J.1    Lee, S.M.2    Song, J.W.3
  • 15
    • 85017340618 scopus 로고    scopus 로고
    • Idiopathic pulmonary fibrosis: The association between the adaptive multiple features method and fibrosis outcomes
    • Salisbury ML, Lynch DA, van Beek EJ, et al. Idiopathic pulmonary fibrosis: the association between the adaptive multiple features method and fibrosis outcomes. Am J Respir Crit Care Med 2017;195:921-9.
    • (2017) Am J Respir Crit Care Med , vol.195 , pp. 921-929
    • Salisbury, M.L.1    Lynch, D.A.2    Van Beek, E.J.3
  • 16
    • 85051187177 scopus 로고    scopus 로고
    • Predicting outcomes in idiopathic pulmonary fibrosis using automated CT analysis
    • Epub ahead of print
    • Jacob J, Bartholmai BJ, Rajagopalan S, et al. Predicting outcomes in idiopathic pulmonary fibrosis using automated CT analysis. Am J Respir Crit Care Med 2018. Epub ahead of print.
    • (2018) Am J Respir Crit Care Med
    • Jacob, J.1    Bartholmai, B.J.2    Rajagopalan, S.3
  • 17
    • 84981321016 scopus 로고    scopus 로고
    • An American Thoracic Society official research statement: Future directions in lung fibrosis research
    • White ES, Borok Z, Brown KK, et al. An American Thoracic Society official research statement: future directions in lung fibrosis research. Am J Respir Crit Care Med 2016;193:792-800.
    • (2016) Am J Respir Crit Care Med , vol.193 , pp. 792-800
    • White, E.S.1    Borok, Z.2    Brown, K.K.3
  • 18
    • 82755161052 scopus 로고    scopus 로고
    • Idiopathic pulmonary fibrosis
    • King TE, Pardo A, Selman M. Idiopathic pulmonary fibrosis. Lancet 2011;378:1949-61.
    • (2011) Lancet , vol.378 , pp. 1949-1961
    • King, T.E.1    Pardo, A.2    Selman, M.3
  • 19
    • 84865113809 scopus 로고    scopus 로고
    • New cellular and molecular mechanisms of lung injury and fibrosis in idiopathic pulmonary fibrosis
    • Fernandez IE, Eickelberg O. New cellular and molecular mechanisms of lung injury and fibrosis in idiopathic pulmonary fibrosis. Lancet 2012;380:680-8.
    • (2012) Lancet , vol.380 , pp. 680-688
    • Fernandez, I.E.1    Eickelberg, O.2
  • 20
    • 85046639818 scopus 로고    scopus 로고
    • Extracellular matrix cross-linking enhances fibroblast growth and protects against matrix proteolysis in lung fibrosis
    • Philp CJ, Siebeke I, Clements D, et al. Extracellular matrix cross-linking enhances fibroblast growth and protects against matrix proteolysis in lung fibrosis. Am J Respir Cell Mol Biol 2018;58:594-603.
    • (2018) Am J Respir Cell Mol Biol , vol.58 , pp. 594-603
    • Philp, C.J.1    Siebeke, I.2    Clements, D.3
  • 21
    • 84962124806 scopus 로고    scopus 로고
    • Role of matrix metalloproteinases in the pathogenesis of idiopathic pulmonary fibrosis
    • Pardo A, Cabrera S, Maldonado M, et al. Role of matrix metalloproteinases in the pathogenesis of idiopathic pulmonary fibrosis. Respir Res 2016;17:23.
    • (2016) Respir Res , vol.17 , pp. 23
    • Pardo, A.1    Cabrera, S.2    Maldonado, M.3
  • 22
    • 84904046300 scopus 로고    scopus 로고
    • Review article: The efficacy of biomarkers in chronic fibroproliferative diseases-Early diagnosis and prognosis, with liver fibrosis as an exemplar
    • Karsdal MA, Krarup H, Sand JM, et al. Review article: the efficacy of biomarkers in chronic fibroproliferative diseases-early diagnosis and prognosis, with liver fibrosis as an exemplar. Aliment Pharmacol Ther 2014;40:233-49.
    • (2014) Aliment Pharmacol Ther , vol.40 , pp. 233-249
    • Karsdal, M.A.1    Krarup, H.2    Sand, J.M.3
  • 23
    • 84927692071 scopus 로고    scopus 로고
    • The role of extracellular matrix quality in pulmonary fibrosis
    • Kristensen JH, Karsdal MA, Genovese F, et al. The role of extracellular matrix quality in pulmonary fibrosis. Respiration 2014;88:487-99.
    • (2014) Respiration , vol.88 , pp. 487-499
    • Kristensen, J.H.1    Karsdal, M.A.2    Genovese, F.3
  • 24
    • 84930865108 scopus 로고    scopus 로고
    • Longitudinal change in collagen degradation biomarkers in idiopathic pulmonary fibrosis: An analysis from the prospective, multicentre PROFILE study
    • Jenkins RG, Simpson JK, Saini G, et al. Longitudinal change in collagen degradation biomarkers in idiopathic pulmonary fibrosis: an analysis from the prospective, multicentre PROFILE study. Lancet Respir Med 2015;3:462-72.
    • (2015) Lancet Respir Med , vol.3 , pp. 462-472
    • Jenkins, R.G.1    Simpson, J.K.2    Saini, G.3
  • 25
    • 49649123154 scopus 로고    scopus 로고
    • BIBF 1120: Triple angiokinase inhibitor with sustained receptor blockade and good antitumor efficacy
    • Hilberg F, Roth GJ, Krssak M, et al. BIBF 1120: triple angiokinase inhibitor with sustained receptor blockade and good antitumor efficacy. Cancer Res 2008;68:4774-82.
    • (2008) Cancer Res , vol.68 , pp. 4774-4782
    • Hilberg, F.1    Roth, G.J.2    Krssak, M.3
  • 26
    • 84898792564 scopus 로고    scopus 로고
    • Antifibrotic and antiinflammatory activity of the tyrosine kinase inhibitor nintedanib in experimental models of lung fibrosis
    • Wollin L, Maillet I, Quesniaux V, et al. Antifibrotic and antiinflammatory activity of the tyrosine kinase inhibitor nintedanib in experimental models of lung fibrosis. J Pharmacol Exp Ther 2014;349:209-20.
    • (2014) J Pharmacol Exp Ther , vol.349 , pp. 209-220
    • Wollin, L.1    Maillet, I.2    Quesniaux, V.3
  • 27
    • 84928995543 scopus 로고    scopus 로고
    • Mode of action of nintedanib in the treatment of idiopathic pulmonary fibrosis
    • Wollin L, Wex E, Pautsch A, et al. Mode of action of nintedanib in the treatment of idiopathic pulmonary fibrosis. Eur Respir J 2015;45:1434-45.
    • (2015) Eur Respir J , vol.45 , pp. 1434-1445
    • Wollin, L.1    Wex, E.2    Pautsch, A.3
  • 28
    • 85014782011 scopus 로고    scopus 로고
    • Effects of nintedanib on the microvascular architecture in a lung fibrosis model
    • Ackermann M, Kim YO, Wagner WL, et al. Effects of nintedanib on the microvascular architecture in a lung fibrosis model. Angiogenesis 2017;20:359-72.
    • (2017) Angiogenesis , vol.20 , pp. 359-372
    • Ackermann, M.1    Kim, Y.O.2    Wagner, W.L.3
  • 29
    • 80053091084 scopus 로고    scopus 로고
    • Efficacy of a tyrosine kinase inhibitor in idiopathic pulmonary fibrosis
    • Richeldi L, Costabel U, Selman M, et al. Efficacy of a tyrosine kinase inhibitor in idiopathic pulmonary fibrosis. N Engl J Med 2011;365:1079-87.
    • (2011) N Engl J Med , vol.365 , pp. 1079-1087
    • Richeldi, L.1    Costabel, U.2    Selman, M.3
  • 30
    • 84901810710 scopus 로고    scopus 로고
    • Efficacy and safety of nintedanib in idiopathic pulmonary fibrosis
    • Richeldi L, du Bois RM, Raghu G, et al. Efficacy and safety of nintedanib in idiopathic pulmonary fibrosis. N Engl J Med 2014;370:2071-82.
    • (2014) N Engl J Med , vol.370 , pp. 2071-2082
    • Richeldi, L.1    Dubois, R.M.2    Raghu, G.3
  • 32
    • 0025886867 scopus 로고
    • The St George's respiratory questionnaire
    • discussion 33-37
    • Jones PW, Quirk FH, Baveystock CM. The St George's respiratory questionnaire. Respir Med 1991;85 Suppl B(Suppl B):25-31. discussion 33-37.
    • (1991) Respir Med , vol.85 , pp. 25-31
    • Jones, P.W.1    Quirk, F.H.2    Baveystock, C.M.3
  • 33
    • 0031912648 scopus 로고    scopus 로고
    • Validation of a new dyspnea measure: The UCSD Shortness of Breath Questionnaire. University of California, San Diego
    • Eakin EG, Resnikoff PM, Prewitt LM, et al. Validation of a new dyspnea measure: the UCSD Shortness of Breath Questionnaire. University of California, San Diego. Chest 1998;113:619-24.
    • (1998) Chest , vol.113 , pp. 619-624
    • Eakin, E.G.1    Resnikoff, P.M.2    Prewitt, L.M.3
  • 34
    • 79952943038 scopus 로고    scopus 로고
    • Pharmacokinetics and metabolism of BIBF 1120 after oral dosing to healthy male volunteers
    • Stopfer P, Rathgen K, Bischoff D, et al. Pharmacokinetics and metabolism of BIBF 1120 after oral dosing to healthy male volunteers. Xenobiotica 2011;41:297-311.
    • (2011) Xenobiotica , vol.41 , pp. 297-311
    • Stopfer, P.1    Rathgen, K.2    Bischoff, D.3
  • 35
    • 84988258715 scopus 로고    scopus 로고
    • Effect of baseline FVC on lung function decline with nintedanib in patients with IPF
    • Maher TM, Flaherty KR, Noble PW, et al. Effect of baseline FVC on lung function decline with nintedanib in patients with IPF. Eur Respir J 2015;46(Suppl. 59):OA4499.
    • (2015) Eur Respir J , vol.46 , pp. OA4499
    • Maher, T.M.1    Flaherty, K.R.2    Noble, P.W.3
  • 36
    • 85017017908 scopus 로고    scopus 로고
    • Nintedanib in patients with idiopathic pulmonary fibrosis and preserved lung volume
    • Kolb M, Richeldi L, Behr J, et al. Nintedanib in patients with idiopathic pulmonary fibrosis and preserved lung volume. Thorax 2017;72:340-6.
    • (2017) Thorax , vol.72 , pp. 340-346
    • Kolb, M.1    Richeldi, L.2    Behr, J.3
  • 37
    • 85029359255 scopus 로고    scopus 로고
    • Acute exacerbation and decline in forced vital capacity are associated with increased mortality in idiopathic pulmonary fibrosis
    • Paterniti MO, Bi Y, Rekić D, et al. Acute exacerbation and decline in forced vital capacity are associated with increased mortality in idiopathic pulmonary fibrosis. Ann Am Thorac Soc 2017;14:1395-402.
    • (2017) Ann Am Thorac Soc , vol.14 , pp. 1395-1402
    • Paterniti, M.O.1    Bi, Y.2    Rekić, D.3
  • 38
    • 84992313036 scopus 로고    scopus 로고
    • Daily home spirometry: An effective tool for detecting progression in idiopathic pulmonary fibrosis
    • Russell AM, Adamali H, Molyneaux PL, et al. Daily home spirometry: an effective tool for detecting progression in idiopathic pulmonary fibrosis. Am J Respir Crit Care Med 2016;194:989-97.
    • (2016) Am J Respir Crit Care Med , vol.194 , pp. 989-997
    • Russell, A.M.1    Adamali, H.2    Molyneaux, P.L.3
  • 39
    • 85026260747 scopus 로고    scopus 로고
    • Home monitoring improves endpoint efficiency in idiopathic pulmonary fibrosis
    • Johannson KA, Vittinghoff E, Morisset J, et al. Home monitoring improves endpoint efficiency in idiopathic pulmonary fibrosis. Eur Respir J 2017;50:1602406.
    • (2017) Eur Respir J , vol.50 , pp. 1602406
    • Johannson, K.A.1    Vittinghoff, E.2    Morisset, J.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.