Clinical and functional efficacy of elexacaftor/tezacaftor/ivacaftor in people with cystic fibrosis carrying the N1303K mutation

•Recent in vitro data suggested that ELX/TEZ/IVA increases N1303K-CFTR function.•8 pwCF that started off label ELX/TEZ/IVA and had significant clinical response, with increase in FEV1 and BMI, though sweat chloride remained in the pathologic value.•Although not listed as ELX/TEZ/IVA responsive mutat...

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Veröffentlicht in:Journal of cystic fibrosis 2023-11, Vol.22 (6), p.1062-1069
Hauptverfasser: Sadras, Ido, Kerem, Eitan, Livnat, Galit, Sarouk, Ifat, Breuer, Oded, Reiter, Joel, Gileles-Hillel, Alex, Inbar, Ori, Cohen, Michael, Gamliel, Ayelet, Stanleigh, Noemie, Gunawardena, Tarini, Bartlett, Claire, Gonska, Tanja, Moraes, Theo, Eckford, Paul D.W., Bear, Christine E., Ratjen, Felix, Kerem, Batsheva, Wilschanski, Michael, Shteinberg, Michal, Cohen-Cymberknoh, Malena
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Sprache:eng
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Zusammenfassung:•Recent in vitro data suggested that ELX/TEZ/IVA increases N1303K-CFTR function.•8 pwCF that started off label ELX/TEZ/IVA and had significant clinical response, with increase in FEV1 and BMI, though sweat chloride remained in the pathologic value.•Although not listed as ELX/TEZ/IVA responsive mutatoin, PwCF carrying the N1303K mutation may have significant clinical benefit by this treatment. Elexacaftor/tezacaftor/ivacaftor (ELX/TEZ/IVA) significantly improves health outcomes in people with cystic fibrosis (pwCF) carrying one or two F508del mutations. According to in vitro assays performed in FRT cells, 178 additional mutations respond to ELX/TEZ/IVA. The N1303K mutation is not included in this list of mutations. Recent in vitro data suggested that ELX/TEZ/IVA increases N1303K-CFTR activity. Based on the in vitro response, eight patients commenced treatment with ELX/TEZ/IVA. Two homozygotes; and six compound heterozygotes N1303K/nonsense or frameshift mutation pwCF were treated off label with ELX/TEZ/IVA. Clinical data before and 8 weeks after starting treatment were prospectively collected. The response to ELX/TEZ/IVA was assessed in intestinal organoids derived from 5 study patients and an additional patient carrying N1303K that is not receiving treatment. Compared to the values before commencing treatment, mean forced expiratory volume in 1 second increased by 18.4 percentage points and 26.5% relative to baseline, mean BMI increased by 0.79 Kg/m2, and mean lung clearance index decreased by 3.6 points and 22.2%. There was no significant change in sweat chloride. Nasal potential difference normalized in four patients and remained abnormal in three. Results in 3D intestinal organoids and 2D nasal epithelial cultures showed a response in CFTR channel activity. This report supports the previously reported in vitro data, performed in human nasal and bronchial epithelial cells and intestinal organoids, that pwCF who carry the N1303K mutation have a significant clinical benefit by ELX/TEZ/IVA treatment.
ISSN:1569-1993
1873-5010
1873-5010
DOI:10.1016/j.jcf.2023.06.001