Elexacaftor-Tezacaftor-Ivacaftor Treatment Reduces Abdominal Symptoms in Cystic Fibrosis-Early results Obtained With the CF-Specific CFAbd-Score

被引:41
作者
Mainz, Jochen G. [1 ,2 ,9 ]
Zagoya, Carlos [1 ]
Polte, Louise [1 ]
Naehrlich, Lutz [3 ,4 ]
Sasse, Lenny [3 ]
Eickmeier, Olaf [5 ]
Smaczny, Christina [5 ]
Barucha, Anton [1 ]
Bechinger, Lilith [1 ]
Duckstein, Franziska [1 ]
Kurzidim, Ludwik [1 ,6 ]
Eschenhagen, Patience [6 ]
Caley, Laura [7 ]
Peckham, Daniel [7 ,8 ]
Schwarz, Carsten [6 ]
机构
[1] Brandenburg Med Sch MHB Univ, Cyst Fibrosis Ctr, Klinikum Westbrandenburg, Brandenburg, Germany
[2] Brandenburg Univ Technol Cottbus Senftenberg, Fac Hlth Sci, Brandenburg Med Sch Theodor Fontane, Joint Fac, Potsdam, Germany
[3] Justus Liebig Univ Giessen, Dept Pediat, Giessen, Germany
[4] Univ Giessen & Marburg Lung Ctr UGMLC, German Ctr Lung Res DZL, Giessen, Germany
[5] Univ Klinikum Frankfurt Main CF Zent, Christiane Herzog CF Zentrum Frankfurt Main, Frankfurt Am Main, Germany
[6] Klinikum Westbrandenburg, CF Zentrum Westbrandenburg, Campus Potsdam, Potsdam, Germany
[7] Univ Leeds, Leeds Inst Med Res St Jamess, Leeds, England
[8] Leeds Teaching Hosp NHS Trust, St Jamess Univ Hosp, Adult Cyst Fibrosis Unit, Leeds, England
[9] Univ Potsdam, Potsdam, Germany
关键词
gastrointestinal; patient reported outcome measure; CFTR modulators; elexacaftor; symptom score; EFFICACY; SAFETY; G551D; THERAPY;
D O I
10.3389/fphar.2022.877118
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Background: The novel and highly effective CFTR modulator combination of elexacaftor-tezacaftor-ivacaftor (ETI) has been shown to improve lung function and body weight in people with Cystic Fibrosis (pwCF) carrying a F508del mutation. However, the impact of these modulators on gastrointestinal (GI) symptoms is relatively unknown. Therefore, the CFAbd-Score was developed and validated following FDA recommendations for development of a PROM including focus groups, multidisciplinary CF specialists, people with CF and their families. The aim of this study was to assess effects of ETI on GI symptoms using the CFAbd-Score.Methods: Gastrointestinal symptoms were prospectively assessed in pwCF using the CFAbd-Score before and up to 26 weeks during therapy. The CFAbd-Score was also administered to a healthy control (HC) group. The one-sided questionnaire includes 28 items grouped in five domains. Data analysis included calculation of scores with a weighting tool, developed according to FDA recommendations.Results: A total of 107 pwCF attended in four CF centres in Germany and four centres in the UK completed the CFAbd-Score on at least two occasions. Results were compared to those obtained from the questionnaire of 45 HCs. Despite differences in demographics, age and proportion of pancreatic insufficiency between German and UK patients, analyses based on linear mixed-effects models at week 24 of ETI therapy revealed that estimated marginal means (EMMs) of total CFAbd-Scores significantly reduced (mean +/- SE: 14.9 +/- 1.2 -> 10.6 +/- 1.4; p < 0.01). Also EMMs of all five domains significantly declined ("pain" 16.3 +/- 1.6 -> 10.2 +/- 2.3, "GERD" 15.8 +/- 1.8 -> 8.2 +/- 1.9, "disorders of bowel movement" 20.9 +/- 1.5 -> 16.0 +/- 1.7, "disorders of appetite" 7.9 +/- 1.1 -> 2.6 +/- 1.1 and "quality of life impairment" 10.1 +/- 1.92 -> 3.9 +/- 1.9). However, during 24 weeks, CF participants' symptoms mostly still did not reach the reference levels of HCs.Discussion: Using the CFAbd-Score, the first PROM specifically developed for assessment of CF-related abdominal symptoms, we demonstrate comprehensive improvements in GI symptoms after initiation of the highly effective modulator therapy ETI.
引用
收藏
页数:11
相关论文
共 37 条
[1]   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
[2]  
[Anonymous], 2009, GUIDANCE IND PATIENT
[3]   CFTR modulator therapies-Effect on life expectancy in people with cystic fibrosis [J].
Balfour-Lynn, I. M. ;
King, J. A. .
PAEDIATRIC RESPIRATORY REVIEWS, 2022, 42 :3-8
[4]   The future of cystic fibrosis care: a global perspective [J].
Bell, Scott C. ;
Mall, Marcus A. ;
Gutierrez, Hector ;
Macek, Milan ;
Madge, Susan ;
Davies, Jane C. ;
Burgel, Pierre-Regis ;
Tullis, Elizabeth ;
Castaos, Claudio ;
Castellani, Carlo ;
Byrnes, Catherine A. ;
Cathcart, Fiona ;
Chotirmall, Sanjay H. ;
Cosgriff, Rebecca ;
Eichler, Irmgard ;
Fajac, Isabelle ;
Goss, Christopher H. ;
Drevinek, Pavel ;
Farrell, Philip M. ;
Gravelle, Anna M. ;
Havermans, Trudy ;
Mayer-Hamblett, Nicole ;
Kashirskaya, Nataliya ;
Kerem, Eitan ;
Mathew, Joseph L. ;
McKone, Edward F. ;
Naehrlich, Lutz ;
Nasr, Samya Z. ;
Oates, Gabriela R. ;
O'Neill, Ciaran ;
Pypops, Ulrike ;
Raraigh, Karen S. ;
Rowe, Steven M. ;
Southern, Kevin W. ;
Sivam, Sheila ;
Stephenson, Anne L. ;
Zampoli, Marco ;
Ratjen, Felix .
LANCET RESPIRATORY MEDICINE, 2020, 8 (01) :65-124
[5]   Cystic fibrosis and the role of gastrointestinal outcome measures in the new era of therapeutic CFTR modulation [J].
Bodewes, Frank A. J. A. ;
Verkade, Henkjan J. ;
Taminiau, Jan A. J. M. ;
Borowitz, Drucy ;
Wilschanski, Michael .
JOURNAL OF CYSTIC FIBROSIS, 2015, 14 (02) :169-177
[6]   Practical approach to the gastrointestinal manifestations of cystic fibrosis [J].
Bolia, Rishi ;
Ooi, Chee Y. ;
Lewindon, Peter ;
Bishop, Jonathan ;
Ranganathan, Sarath ;
Harrison, Jo ;
Ford, Kristyn ;
van der Haak, Natalie ;
Oliver, Mark R. .
JOURNAL OF PAEDIATRICS AND CHILD HEALTH, 2018, 54 (06) :609-619
[7]   Use of a mobile application for self-management of pancreatic enzyme replacement therapy is associated with improved gastro-intestinal related quality of life in children with Cystic Fibrosis [J].
Boon, M. ;
Calvo-Lerma, J. ;
Claes, I ;
Havermans, T. ;
Asseiceira, I ;
Bulfamante, A. ;
Garriga, M. ;
Masip, E. ;
van Schijndel, B. A. M. ;
Fornes, V ;
Barreto, C. ;
Colombo, C. ;
Crespo, P. ;
Vicente, S. ;
Janssens, H. ;
Hulst, J. ;
Witters, P. ;
Nobili, R. ;
Pereira, L. ;
Ruperto, M. ;
Van der Wiel, E. ;
Mainz, J. G. ;
De Boeck, K. ;
Ribes-Koninckx, C. .
JOURNAL OF CYSTIC FIBROSIS, 2020, 19 (04) :562-568
[8]   Safety, pharmacokinetics, and pharmacodynamics of ivacaftor in patients aged 2-5 years with cystic fibrosis and a CFTR gating mutation (KIWI): an open-label, single-arm study [J].
Davies, Jane C. ;
Cunningham, Steve ;
Harris, William T. ;
Lapey, Allen ;
Regelmann, Warren E. ;
Sawicki, Gregory S. ;
Southern, Kevin W. ;
Robertson, Sarah ;
Green, Yulia ;
Cooke, Jon ;
Rosenfeld, Margaret .
LANCET RESPIRATORY MEDICINE, 2016, 4 (02) :107-115
[9]   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
[10]   The World Health Organization global database on child growth and malnutrition:: Methodology and applications [J].
de Onis, M ;
Blössner, M .
INTERNATIONAL JOURNAL OF EPIDEMIOLOGY, 2003, 32 (04) :518-526