A randomised crossover trial of tezacaftor-ivacaftor for gut dysfunction in cystic fibrosis with magnetic resonance imaging (MRI) outcomes: a pilot study.

NIHR open research Pub Date : 2024-03-19 eCollection Date: 2023-01-01 DOI:10.3310/nihropenres.13510.2
Christabella Ng, Neele S Dellschaft, Caroline Hoad, Luca Marciani, Robin Spiller, Colin Crooks, Trevor Hill, Alex Menys, Jochen G Mainz, Helen Barr, Penny A Gowland, Giles Major, Alan R Smyth
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Abstract

Background: People with cystic fibrosis (CF) can experience recurrent chest infections, pancreatic exocrine insufficiency and gastrointestinal symptoms. New cystic fibrosis transmembrane conductance regulator (CFTR) modulator drugs improve lung function but gastrointestinal effects are unclear. We aimed to see if a CFTR modulator (tezacaftor-ivacaftor,TEZ/IVA) improves gastrointestinal outcomes in CF.

Methods: We conducted a randomised, double-blind, placebo-controlled, two-period crossover trial (2019-2020) at Nottingham University Hospitals. The effects of TEZ/IVA on gut physiology were measured using MRI. Participants were randomly assigned to treatment sequences AB or BA (A:TEZ/IVA, B:placebo, each 28 days), with a 28-day washout period. Participants had serial MRI scans at baseline and after 19-23 days of each treatment. Due to the COVID-19 pandemic, a protocol amendment allowed for observer-blind comparisons prior to and during TEZ/IVA. In such cases, participants were not blind to the treatment but researchers remained blind. The primary outcome was oro-caecal transit time (OCTT). Secondary outcomes included MRI metrics, symptoms and stool biomarkers.

Results: We randomised 13 participants. Before the COVID-19 pandemic 8 participants completed the full protocol and 1 dropped out. The remaining 4 participants followed the amended protocol. There were no significant differences between placebo and TEZ/IVA for OCTT (TEZ/IVA >360minutes [225,>360] vs. placebo 330minutes [285,>360], p=0.8) or secondary outcomes. There were no adverse events.

Conclusions: Our data contribute to a research gap in the extra-pulmonary effects of CFTR modulators. We found no effect after TEZ/IVA on MRI metrics of gut function, GI symptoms or stool calprotectin. Effects might be detectable with larger studies, longer treatment or more effective CFTR modulators.

Clinicaltrialsgov registration: NCT04006873 (02/07/2019).

针对囊性纤维化肠道功能紊乱的 tezacaftor-ivacaftor 与磁共振成像(MRI)结果的随机交叉试验:一项试点研究。
背景:囊性纤维化(CF)患者会反复出现胸部感染、胰腺外分泌功能不全和胃肠道症状。新型囊性纤维化跨膜传导调节器(CFTR)调节剂药物可改善肺功能,但对胃肠道的影响尚不明确。我们的目的是研究 CFTR 调节剂(tezacaftor-ivacaftor,TEZ/IVA)是否能改善 CF 患者的胃肠道症状:我们在诺丁汉大学医院开展了一项随机、双盲、安慰剂对照、两期交叉试验(2019-2020年)。使用核磁共振成像测量 TEZ/IVA 对肠道生理学的影响。参与者被随机分配到AB或BA治疗序列(A:TEZ/IVA,B:安慰剂,各28天),并有28天的冲洗期。参试者在基线和每个疗程的 19-23 天后接受连续 MRI 扫描。由于 COVID-19 大流行,方案修正案允许在 TEZ/IVA 之前和期间进行观察者盲法比较。在这种情况下,参与者对治疗不设盲区,但研究人员仍保持盲区。主要结果是大便转运时间(OCTT)。次要结果包括核磁共振成像指标、症状和粪便生物标志物:我们随机抽取了 13 名参与者。在 COVID-19 大流行之前,8 名参与者完成了全部方案,1 人退出。其余 4 人按照修订后的方案进行了治疗。安慰剂和 TEZ/IVA 在 OCTT(TEZ/IVA >360 分钟 [225,>360] vs. 安慰剂 330 分钟 [285,>360], p=0.8)或次要结果方面无明显差异。无不良事件发生:我们的数据填补了CFTR调节剂肺外效应方面的研究空白。我们发现TEZ/IVA对肠道功能的核磁共振指标、消化道症状或粪便钙蛋白没有影响。如果进行更大规模的研究、延长治疗时间或使用更有效的CFTR调节剂,可能会发现效果:NCT04006873 (02/07/2019).
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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