Abstract

Forskolin-induced swelling of patient-derived organoids has been used to measure patient-specific CFTR function and CFTR modulator response. We present a case where CFTR function assessment in intestinal organoids was decisive for a patients' acceptance to a compassionate use program. A 56 years old female with cystic fibrosis compound heterozygous for F508del and a rare CFTR allele (c.3717+5G>T) experienced rapid clinical deterioration. The forskolin-induced swelling assay on her rectal organoids was used to confirm that the rare mutation is a minimal residual function mutation, and that other CFTR modulators would not likely be effective. Based on these two criteria and her clinical status, she was accepted for compassionate use of elexacaftor/tezacaftor/ivacaftor and showed improvement in all clinical parameters. This reports describes a first example that intestinal organoids were used to identify a previously unknown CFTR mutation as a minimal function mutation. The individual FIS-based definition of minimal residual function, response to ele/tez/iva and/or lack of response to other CFTR modulating drugs, may thus provide a tool for access to ele/tez/iva treatment for people with rare genotypes.

Highlights

  • Elexacaftor in combination with tezacaftor and ivacaftor is a generation CFTR modulator treatment and has been approved for treatment of cystic fibrosis in October 2019 in the US and in August 2020 in the EU

  • Many mutations associated with cystic fibrosis (CF) remain uncharacterized and have not been functionally annotated [3]

  • Patient-derived intestinal organoids facilitate the measurement of individual CFTR function through the forskolin-induced swelling (FIS) assay, enabling both the assessment of CFTR residual function and the effects of CFTR modulators. [4,5]

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Summary

Background

Forskolin-induced swelling of patient-derived organoids has been used to measure patientspecific CFTR function and CFTR modulator response. We present a case where CFTR function assessment in intestinal organoids was decisive for a patients’ acceptance to a compassionate use program. The forskolin-induced swelling assay on her rectal organoids was used to confirm that the rare mutation is a minimal residual function mutation, and that other CFTR modulators would not likely be effective. Based on these two criteria and her clinical status, she was accepted for compassionate use of elexacaftor/tezacaftor/ivacaftor and showed improvement in all clinical parameters. The individual FIS-based definition of minimal residual function, response to ele/tez/iva and/or lack of response to other CFTR modulating drugs, may provide a tool for access to ele/tez/iva treatment for people with rare genotypes

Introduction
Case description
Discussion
Conclusion
Findings
Declaration of competing interest
Full Text
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