ToxNav germline genetic testing and PROMinet digital mobile application toxicity monitoring: Results of a prospective single-center clinical utility study-PRECISE study.

<p><strong>INTRODUCTION:</strong> In this study (PRECISE), we assess the clinical utility of a germline DNA sequencing-based test (ToxNav) for mutations in DPYD and ENOSF1 genes to alter clinician-prescribed fluoropyrimidine doses and the use of a digital application (PROMinet) to...

Description complète

Détails bibliographiques
Auteurs principaux: Lee, L, Starkey, T, Sivakumar, S, Fotheringham, S, Mozolowski, G, Shearwood, V, Palles, C, Camilleri, P, Church, D, Kerr, R, Kerr, D
Format: Conference item
Publié: Wiley 2019
_version_ 1826288756713324544
author Lee, L
Starkey, T
Sivakumar, S
Fotheringham, S
Mozolowski, G
Shearwood, V
Palles, C
Camilleri, P
Church, D
Kerr, R
Kerr, D
author_facet Lee, L
Starkey, T
Sivakumar, S
Fotheringham, S
Mozolowski, G
Shearwood, V
Palles, C
Camilleri, P
Church, D
Kerr, R
Kerr, D
author_sort Lee, L
collection OXFORD
description <p><strong>INTRODUCTION:</strong> In this study (PRECISE), we assess the clinical utility of a germline DNA sequencing-based test (ToxNav) for mutations in DPYD and ENOSF1 genes to alter clinician-prescribed fluoropyrimidine doses and the use of a digital application (PROMinet) to record patient-reported chemotherapy toxicity.</p> <p><strong>MATERIALS AND METHODS:</strong> Adult patients with a histological diagnosis of colorectal cancer (CRC) who consented to fluoropyrimidine-based chemotherapy were recruited prospectively and given a digital application to monitor and record associated toxicities. Patient samples were analyzed for 18 germline coding variants in DPYD and 1 ENOSF1 variant.</p> <p><strong>RESULTS:</strong> Genetic testing was performed for 60 patients and identified one patient at increased risk of fluoropyrimidine-based toxicities. Uptake of genetic testing was high and results were available on average 17 days from initial clinical encounter. Patient-reported chemotherapy toxicity identified differences in 5-fluorouracil vs capecitabine regime profiles and identified profiles associated with subsequent need for chemotherapy dose reduction and hospital admission.</p> <p><strong>DISCUSSION:</strong> The PRECISE clinical trial demonstrated that a germline DNA sequencing-based test can provide clinically relevant information to alter clinicians' fluoropyrimidine prescription. The study also obtained high volume, high granularity patient-reported toxicity data that might allow the improvement and personalization of chemotherapy management.</p>
first_indexed 2024-03-07T02:18:31Z
format Conference item
id oxford-uuid:a3182d3f-fa83-4a3e-af1d-433fd0ab8b9b
institution University of Oxford
last_indexed 2024-03-07T02:18:31Z
publishDate 2019
publisher Wiley
record_format dspace
spelling oxford-uuid:a3182d3f-fa83-4a3e-af1d-433fd0ab8b9b2022-03-27T02:24:30ZToxNav germline genetic testing and PROMinet digital mobile application toxicity monitoring: Results of a prospective single-center clinical utility study-PRECISE study.Conference itemhttp://purl.org/coar/resource_type/c_5794uuid:a3182d3f-fa83-4a3e-af1d-433fd0ab8b9bSymplectic Elements at OxfordWiley2019Lee, LStarkey, TSivakumar, SFotheringham, SMozolowski, GShearwood, VPalles, CCamilleri, PChurch, DKerr, RKerr, D<p><strong>INTRODUCTION:</strong> In this study (PRECISE), we assess the clinical utility of a germline DNA sequencing-based test (ToxNav) for mutations in DPYD and ENOSF1 genes to alter clinician-prescribed fluoropyrimidine doses and the use of a digital application (PROMinet) to record patient-reported chemotherapy toxicity.</p> <p><strong>MATERIALS AND METHODS:</strong> Adult patients with a histological diagnosis of colorectal cancer (CRC) who consented to fluoropyrimidine-based chemotherapy were recruited prospectively and given a digital application to monitor and record associated toxicities. Patient samples were analyzed for 18 germline coding variants in DPYD and 1 ENOSF1 variant.</p> <p><strong>RESULTS:</strong> Genetic testing was performed for 60 patients and identified one patient at increased risk of fluoropyrimidine-based toxicities. Uptake of genetic testing was high and results were available on average 17 days from initial clinical encounter. Patient-reported chemotherapy toxicity identified differences in 5-fluorouracil vs capecitabine regime profiles and identified profiles associated with subsequent need for chemotherapy dose reduction and hospital admission.</p> <p><strong>DISCUSSION:</strong> The PRECISE clinical trial demonstrated that a germline DNA sequencing-based test can provide clinically relevant information to alter clinicians' fluoropyrimidine prescription. The study also obtained high volume, high granularity patient-reported toxicity data that might allow the improvement and personalization of chemotherapy management.</p>
spellingShingle Lee, L
Starkey, T
Sivakumar, S
Fotheringham, S
Mozolowski, G
Shearwood, V
Palles, C
Camilleri, P
Church, D
Kerr, R
Kerr, D
ToxNav germline genetic testing and PROMinet digital mobile application toxicity monitoring: Results of a prospective single-center clinical utility study-PRECISE study.
title ToxNav germline genetic testing and PROMinet digital mobile application toxicity monitoring: Results of a prospective single-center clinical utility study-PRECISE study.
title_full ToxNav germline genetic testing and PROMinet digital mobile application toxicity monitoring: Results of a prospective single-center clinical utility study-PRECISE study.
title_fullStr ToxNav germline genetic testing and PROMinet digital mobile application toxicity monitoring: Results of a prospective single-center clinical utility study-PRECISE study.
title_full_unstemmed ToxNav germline genetic testing and PROMinet digital mobile application toxicity monitoring: Results of a prospective single-center clinical utility study-PRECISE study.
title_short ToxNav germline genetic testing and PROMinet digital mobile application toxicity monitoring: Results of a prospective single-center clinical utility study-PRECISE study.
title_sort toxnav germline genetic testing and prominet digital mobile application toxicity monitoring results of a prospective single center clinical utility study precise study
work_keys_str_mv AT leel toxnavgermlinegenetictestingandprominetdigitalmobileapplicationtoxicitymonitoringresultsofaprospectivesinglecenterclinicalutilitystudyprecisestudy
AT starkeyt toxnavgermlinegenetictestingandprominetdigitalmobileapplicationtoxicitymonitoringresultsofaprospectivesinglecenterclinicalutilitystudyprecisestudy
AT sivakumars toxnavgermlinegenetictestingandprominetdigitalmobileapplicationtoxicitymonitoringresultsofaprospectivesinglecenterclinicalutilitystudyprecisestudy
AT fotheringhams toxnavgermlinegenetictestingandprominetdigitalmobileapplicationtoxicitymonitoringresultsofaprospectivesinglecenterclinicalutilitystudyprecisestudy
AT mozolowskig toxnavgermlinegenetictestingandprominetdigitalmobileapplicationtoxicitymonitoringresultsofaprospectivesinglecenterclinicalutilitystudyprecisestudy
AT shearwoodv toxnavgermlinegenetictestingandprominetdigitalmobileapplicationtoxicitymonitoringresultsofaprospectivesinglecenterclinicalutilitystudyprecisestudy
AT pallesc toxnavgermlinegenetictestingandprominetdigitalmobileapplicationtoxicitymonitoringresultsofaprospectivesinglecenterclinicalutilitystudyprecisestudy
AT camillerip toxnavgermlinegenetictestingandprominetdigitalmobileapplicationtoxicitymonitoringresultsofaprospectivesinglecenterclinicalutilitystudyprecisestudy
AT churchd toxnavgermlinegenetictestingandprominetdigitalmobileapplicationtoxicitymonitoringresultsofaprospectivesinglecenterclinicalutilitystudyprecisestudy
AT kerrr toxnavgermlinegenetictestingandprominetdigitalmobileapplicationtoxicitymonitoringresultsofaprospectivesinglecenterclinicalutilitystudyprecisestudy
AT kerrd toxnavgermlinegenetictestingandprominetdigitalmobileapplicationtoxicitymonitoringresultsofaprospectivesinglecenterclinicalutilitystudyprecisestudy