Correlation of sweat chloride and percent predicted FEV1 in cystic fibrosis patients treated with ivacaftor

被引:75
作者
Fidler, Meredith C. [1 ]
Beusmans, Jack [2 ]
Panorchan, Paul [2 ]
Van Goor, Fredrick [1 ]
机构
[1] Vertex Pharmaceut LLC, 11010 Torreyanna Rd, San Diego, CA 92121 USA
[2] Vertex Pharmaceut Inc, 50 Northern Ave, Boston, MA 02210 USA
关键词
Cystic fibrosis; Ivacaftor; Sweat chloride; FEV1; EFFICACY; SAFETY; IDENTIFICATION; GENE;
D O I
10.1016/j.jcf.2016.10.002
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Ivacaftor, a CFTR potentiator that enhances chloride transport by acting directly on CFTR to increase its channel gating activity, has been evaluated in patients with different CFTR mutations. Several previous analyses have reported no statistical correlation between change from baseline in ppFEV(1) and reduction in sweat chloride levels for individuals treated with ivacaftor. The objective of the post hoc analysis described here was to expand upon previous analyses and evaluate the correlation between sweat chloride levels and absolute ppFEV(1) changes across multiple cohorts of patients with different CF-causing mutations who were treated with ivacaftor. The goal of the analysis was to help define the potential value of sweat chloride as a pharmacodynamic biomarker for use in CFTR modulator trials. For any given study, reductions in sweat chloride levels and improvements in absolute ppFEV(1) were not correlated for individual patients. However, when the data from all studies were combined, a statistically significant correlation between sweat chloride levels and ppFEV(1) changes was observed (p < 0.0001). Thus, sweat chloride level changes in response to potentiation of the CFTR protein by ivacaftor appear to be a predictive pharmacodynamic biomarker of lung function changes on a population basis but are unsuitable for the prediction of treatment benefits for individuals. (C) 2016 The Authors. Published by Elsevier B.V. on behalf of European Cystic Fibrosis Society. This is an open access article under the CC BY-NC-ND license.
引用
收藏
页码:41 / 44
页数:4
相关论文
共 17 条
[1]   Sweat chloride as a biomarker of CFTR activity: Proof of concept and ivacaftor clinical trial data [J].
Accurso, Frank J. ;
Van Goor, Fredrick ;
Zha, Jiuhong ;
Stone, Anne J. ;
Dong, Qunming ;
Ordonez, Claudia L. ;
Rowe, Steven M. ;
Clancy, John Paul ;
Konstan, Michael W. ;
Hoch, Heather E. ;
Heltshe, Sonya L. ;
Ramsey, Bonnie W. ;
Campbell, Preston W. ;
Ashlock, Melissa A. .
JOURNAL OF CYSTIC FIBROSIS, 2014, 13 (02) :139-147
[2]   Effect of VX-770 in Persons with Cystic Fibrosis and the G551D-CFTR Mutation [J].
Accurso, Frank J. ;
Rowe, Steven M. ;
Clancy, J. P. ;
Boyle, Michael P. ;
Dunitz, Jordan M. ;
Durie, Peter R. ;
Sagel, Scott D. ;
Hornick, Douglas B. ;
Konstan, Michael W. ;
Donaldson, Scott H. ;
Moss, Richard B. ;
Pilewski, Joseph M. ;
Rubenstein, Ronald C. ;
Uluer, Ahmet Z. ;
Aitken, Moira L. ;
Freedman, Steven D. ;
Rose, Lynn M. ;
Mayer-Hamblett, Nicole ;
Dong, Qunming ;
Zha, Jiuhong ;
Stone, Anne J. ;
Olson, Eric R. ;
Ordonez, Claudia L. ;
Campbell, Preston W. ;
Ashlock, Melissa A. ;
Ramsey, Bonnie W. .
NEW ENGLAND JOURNAL OF MEDICINE, 2010, 363 (21) :1991-2003
[3]   Sweat chloride is not a useful marker of clinical response to Ivacaftor [J].
Barry, Peter J. ;
Jones, Andrew M. ;
Webb, Anthony K. ;
Horsley, Alexander R. .
THORAX, 2014, 69 (06) :586-U149
[4]  
Collaco JM, 2016, AM J RESP CRIT CARE
[5]   Efficacy and Safety of Ivacaftor in Patients Aged 6 to 11 Years with Cystic Fibrosis with a G551D Mutation [J].
Davies, Jane C. ;
Wainwright, Claire E. ;
Canny, Gerard J. ;
Chilvers, Mark A. ;
Howenstine, Michelle S. ;
Munck, Anne ;
Mainz, Jochen G. ;
Rodriguez, Sally ;
Li, Haihong ;
Yen, Karl ;
Ordonez, Claudia L. ;
Ahrens, Richard .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2013, 187 (11) :1219-1225
[6]   Efficacy and safety of ivacaftor in patients with cystic fibrosis and a non-G551D gating mutation [J].
De Boeck, Kris ;
Munck, Anne ;
Walker, Seth ;
Faro, Albert ;
Hiatt, Peter ;
Gilmartin, Geoffrey ;
Higgins, Mark .
JOURNAL OF CYSTIC FIBROSIS, 2014, 13 (06) :674-680
[7]   Change in Sweat Chloride as a Clinical End Point in Cystic Fibrosis Clinical Trials The Ivacaftor Experience [J].
Durmowicz, Anthony G. ;
Witzmann, Kimberly A. ;
Rosebraugh, Curtis J. ;
Chowdhury, Badrul A. .
CHEST, 2013, 143 (01) :14-18
[8]   Ivacaftor in Subjects With Cystic Fibrosis Who Are Homozygous for the F508del-CFTR Mutation [J].
Flume, Patrick A. ;
Liou, Theodore G. ;
Borowitz, Drucy S. ;
Li, Haihong ;
Yen, Karl ;
Ordonez, Claudia L. ;
Geller, David E. .
CHEST, 2012, 142 (03) :718-724
[9]   IDENTIFICATION OF THE CYSTIC-FIBROSIS GENE - GENETIC-ANALYSIS [J].
KEREM, BS ;
ROMMENS, JM ;
BUCHANAN, JA ;
MARKIEWICZ, D ;
COX, TK ;
CHAKRAVARTI, A ;
BUCHWALD, M ;
TSUI, LC .
SCIENCE, 1989, 245 (4922) :1073-1080
[10]   VARIATION OF SWEAT SODIUM AND CHLORIDE WITH AGE IN CYSTIC-FIBROSIS AND NORMAL-POPULATIONS - FURTHER INVESTIGATIONS IN EQUIVOCAL CASES [J].
KIRK, JM ;
KESTON, M ;
MCINTOSH, I ;
ALESSA, S .
ANNALS OF CLINICAL BIOCHEMISTRY, 1992, 29 :145-152