Recovery of lung function following a pulmonary exacerbation in patients with cystic fibrosis and the G551D-CFTR mutation treated with ivacaftor

被引:38
作者
Flume, Patrick A. [1 ,2 ]
Wainwright, Claire E. [3 ,4 ]
Tullis, D. Elizabeth [5 ]
Rodriguez, Sally [6 ]
Niknian, Minoo [7 ]
Higgins, Mark [8 ]
Davies, Jane C. [9 ,10 ]
Wagener, Jeffrey S. [11 ]
机构
[1] Med Univ South Carolina, Dept Med, 96 Jonathan Lucas St,Room 812-CSB,MSC 630, Charleston, SC 29425 USA
[2] Med Univ South Carolina, Dept Pediat, 96 Jonathan Lucas St,Room 812-CSB,MSC 630, Charleston, SC 29425 USA
[3] Univ Queensland, Ctr Child Hlth Res, Level 7,Graham St, South Brisbane, Qld 4101, Australia
[4] Lady Cilento Childrens Hosp, 501 Stanley St, South Brisbane, Qld 4101, Australia
[5] Univ Toronto, Li Ka Shing Knowledge Inst, St Michaels Hosp, Div Respirol,Keenan Res Ctr,Dept Med, 1 Kings Coll Circle,6263 Med Sci Bldg, Toronto, ON M5S 1A8, Canada
[6] Johnson & Johnson Med Devices, 325 Paramount Dr, Raynham, MA 02767 USA
[7] Vertex Pharmaceut Inc, 50 Northern Ave, Boston, MA 02210 USA
[8] Vertex Pharmaceut Europe Ltd, 86-88 Jubilee Ave,Milton Pk, Abingdon OX14 4RW, Oxon, England
[9] Imperial Coll, Natl Heart & Lung Inst, London, England
[10] Royal Brompton & Harefield Natl Hlth Serv Fdn Tru, Dept Pediat Resp Med, Sydney St, London SW3 6NP, England
[11] Univ Colorado, Sch Med, Dept Pediat, 13123 E 16th Ave, Aurora, CO 80045 USA
关键词
Cystic fibrosis; Pulmonary exacerbations; Ivacaftor; Cystic fibrosis transmembrane conductance regulator; Pulmonary function; CFTR POTENTIATOR; CONTROLLED-TRIAL; CHILDREN; DECLINE; PSEUDOMONAS; IMPACT; FEV1;
D O I
10.1016/j.jcf.2017.06.002
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Background: Pulmonary exacerbations (PEx) are associated with acute loss of lung function that is often not recovered after treatment. We investigated lung function recovery following PEx for ivacaftor- and placebo-treated subjects. Methods: Short- and long-term pulmonary function recovery data after PEx were summarized from a placebo-controlled trial in 161 cystic fibrosis patients 12 years old with the G551D-CFTR mutation (NCT00909532). Short-term recovery was measured 2 to 8 weeks after treatment, and long-term recovery was determined at the end-of-study, both compared with baseline measured just prior to the PEx. Results: Fewer patients receiving ivacaftor experienced a PEx than patients receiving placebo (33.7% vs. 56.4%; P = 0.004) and had a lower adjusted incidence rate of PEx (0.589 vs. 1.382; P < 0.001). The proportion of PEx followed by full short-term recovery of percent predicted forced expiratory volume in 1 s was similar (ivacaftor vs. placebo, 57.1% vs. 53.7), as was the proportion of patients having long-term recovery (46.4% vs. 47.7%). Conclusions: Ivacaftor treatment reduces the frequency of PEx but does not improve on the rate of complete lung function recovery after PEx when compared with placebo. (C) 2017 European Cystic Fibrosis Society. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:83 / 88
页数:6
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