Cargando…
MyLynch: A Patient-Facing Clinical Decision Support Tool for Genetically-Guided Personalized Medicine in Lynch Syndrome
SIMPLE SUMMARY: Lynch syndrome (LS) is associated with varying cancer risks depending on which of the five causative genes harbors a pathogenic variant; however, lifestyle and medical interventions provide options to lower those risks. We developed MyLynch, a patient-facing clinical decision support...
Autores principales: | , , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9856567/ https://www.ncbi.nlm.nih.gov/pubmed/36672340 http://dx.doi.org/10.3390/cancers15020391 |
_version_ | 1784873663390023680 |
---|---|
author | Knapp, Stephen T. Revette, Anna Underhill-Blazey, Meghan Stopfer, Jill E. Ukaegbu, Chinedu I. Poulin, Cole Parenteau, Madison Syngal, Sapna Bae, Eunchan Bickmore, Timothy Hampel, Heather Idos, Gregory E. Parmigiani, Giovanni Yurgelun, Matthew B. Braun, Danielle |
author_facet | Knapp, Stephen T. Revette, Anna Underhill-Blazey, Meghan Stopfer, Jill E. Ukaegbu, Chinedu I. Poulin, Cole Parenteau, Madison Syngal, Sapna Bae, Eunchan Bickmore, Timothy Hampel, Heather Idos, Gregory E. Parmigiani, Giovanni Yurgelun, Matthew B. Braun, Danielle |
author_sort | Knapp, Stephen T. |
collection | PubMed |
description | SIMPLE SUMMARY: Lynch syndrome (LS) is associated with varying cancer risks depending on which of the five causative genes harbors a pathogenic variant; however, lifestyle and medical interventions provide options to lower those risks. We developed MyLynch, a patient-facing clinical decision support (CDS) web application that applies genetically-guided personalized medicine (GPM) for individuals with LS. MyLynch informs LS patients of their personal cancer risks, educates patients on relevant interventions, and provides patients with adjusted risk estimates depending on the interventions they choose to pursue. MyLynch can improve risk communication between patients and providers while also encouraging communication among relatives with the goal of increasing cascade testing. As genetic panel testing becomes more widely available, GPM will play an increasingly important role in patient care, and CDS tools offer patients and providers tailored information to inform decision-making. MyLynch provides personalized cancer risk estimates and interventions to lower these risks for patients with LS. ABSTRACT: Lynch syndrome (LS) is a hereditary cancer susceptibility condition associated with varying cancer risks depending on which of the five causative genes harbors a pathogenic variant; however, lifestyle and medical interventions provide options to lower those risks. We developed MyLynch, a patient-facing clinical decision support (CDS) web application that applies genetically-guided personalized medicine (GPM) for individuals with LS. The tool was developed in R Shiny through a patient-focused iterative design process. The knowledge base used to estimate patient-specific risk leveraged a rigorously curated literature review. MyLynch informs LS patients of their personal cancer risks, educates patients on relevant interventions, and provides patients with adjusted risk estimates, depending on the interventions they choose to pursue. MyLynch can improve risk communication between patients and providers while also encouraging communication among relatives with the goal of increasing cascade testing. As genetic panel testing becomes more widely available, GPM will play an increasingly important role in patient care, and CDS tools offer patients and providers tailored information to inform decision-making. MyLynch provides personalized cancer risk estimates and interventions to lower these risks for patients with LS. |
format | Online Article Text |
id | pubmed-9856567 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-98565672023-01-21 MyLynch: A Patient-Facing Clinical Decision Support Tool for Genetically-Guided Personalized Medicine in Lynch Syndrome Knapp, Stephen T. Revette, Anna Underhill-Blazey, Meghan Stopfer, Jill E. Ukaegbu, Chinedu I. Poulin, Cole Parenteau, Madison Syngal, Sapna Bae, Eunchan Bickmore, Timothy Hampel, Heather Idos, Gregory E. Parmigiani, Giovanni Yurgelun, Matthew B. Braun, Danielle Cancers (Basel) Article SIMPLE SUMMARY: Lynch syndrome (LS) is associated with varying cancer risks depending on which of the five causative genes harbors a pathogenic variant; however, lifestyle and medical interventions provide options to lower those risks. We developed MyLynch, a patient-facing clinical decision support (CDS) web application that applies genetically-guided personalized medicine (GPM) for individuals with LS. MyLynch informs LS patients of their personal cancer risks, educates patients on relevant interventions, and provides patients with adjusted risk estimates depending on the interventions they choose to pursue. MyLynch can improve risk communication between patients and providers while also encouraging communication among relatives with the goal of increasing cascade testing. As genetic panel testing becomes more widely available, GPM will play an increasingly important role in patient care, and CDS tools offer patients and providers tailored information to inform decision-making. MyLynch provides personalized cancer risk estimates and interventions to lower these risks for patients with LS. ABSTRACT: Lynch syndrome (LS) is a hereditary cancer susceptibility condition associated with varying cancer risks depending on which of the five causative genes harbors a pathogenic variant; however, lifestyle and medical interventions provide options to lower those risks. We developed MyLynch, a patient-facing clinical decision support (CDS) web application that applies genetically-guided personalized medicine (GPM) for individuals with LS. The tool was developed in R Shiny through a patient-focused iterative design process. The knowledge base used to estimate patient-specific risk leveraged a rigorously curated literature review. MyLynch informs LS patients of their personal cancer risks, educates patients on relevant interventions, and provides patients with adjusted risk estimates, depending on the interventions they choose to pursue. MyLynch can improve risk communication between patients and providers while also encouraging communication among relatives with the goal of increasing cascade testing. As genetic panel testing becomes more widely available, GPM will play an increasingly important role in patient care, and CDS tools offer patients and providers tailored information to inform decision-making. MyLynch provides personalized cancer risk estimates and interventions to lower these risks for patients with LS. MDPI 2023-01-06 /pmc/articles/PMC9856567/ /pubmed/36672340 http://dx.doi.org/10.3390/cancers15020391 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Knapp, Stephen T. Revette, Anna Underhill-Blazey, Meghan Stopfer, Jill E. Ukaegbu, Chinedu I. Poulin, Cole Parenteau, Madison Syngal, Sapna Bae, Eunchan Bickmore, Timothy Hampel, Heather Idos, Gregory E. Parmigiani, Giovanni Yurgelun, Matthew B. Braun, Danielle MyLynch: A Patient-Facing Clinical Decision Support Tool for Genetically-Guided Personalized Medicine in Lynch Syndrome |
title | MyLynch: A Patient-Facing Clinical Decision Support Tool for Genetically-Guided Personalized Medicine in Lynch Syndrome |
title_full | MyLynch: A Patient-Facing Clinical Decision Support Tool for Genetically-Guided Personalized Medicine in Lynch Syndrome |
title_fullStr | MyLynch: A Patient-Facing Clinical Decision Support Tool for Genetically-Guided Personalized Medicine in Lynch Syndrome |
title_full_unstemmed | MyLynch: A Patient-Facing Clinical Decision Support Tool for Genetically-Guided Personalized Medicine in Lynch Syndrome |
title_short | MyLynch: A Patient-Facing Clinical Decision Support Tool for Genetically-Guided Personalized Medicine in Lynch Syndrome |
title_sort | mylynch: a patient-facing clinical decision support tool for genetically-guided personalized medicine in lynch syndrome |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9856567/ https://www.ncbi.nlm.nih.gov/pubmed/36672340 http://dx.doi.org/10.3390/cancers15020391 |
work_keys_str_mv | AT knappstephent mylynchapatientfacingclinicaldecisionsupporttoolforgeneticallyguidedpersonalizedmedicineinlynchsyndrome AT revetteanna mylynchapatientfacingclinicaldecisionsupporttoolforgeneticallyguidedpersonalizedmedicineinlynchsyndrome AT underhillblazeymeghan mylynchapatientfacingclinicaldecisionsupporttoolforgeneticallyguidedpersonalizedmedicineinlynchsyndrome AT stopferjille mylynchapatientfacingclinicaldecisionsupporttoolforgeneticallyguidedpersonalizedmedicineinlynchsyndrome AT ukaegbuchinedui mylynchapatientfacingclinicaldecisionsupporttoolforgeneticallyguidedpersonalizedmedicineinlynchsyndrome AT poulincole mylynchapatientfacingclinicaldecisionsupporttoolforgeneticallyguidedpersonalizedmedicineinlynchsyndrome AT parenteaumadison mylynchapatientfacingclinicaldecisionsupporttoolforgeneticallyguidedpersonalizedmedicineinlynchsyndrome AT syngalsapna mylynchapatientfacingclinicaldecisionsupporttoolforgeneticallyguidedpersonalizedmedicineinlynchsyndrome AT baeeunchan mylynchapatientfacingclinicaldecisionsupporttoolforgeneticallyguidedpersonalizedmedicineinlynchsyndrome AT bickmoretimothy mylynchapatientfacingclinicaldecisionsupporttoolforgeneticallyguidedpersonalizedmedicineinlynchsyndrome AT hampelheather mylynchapatientfacingclinicaldecisionsupporttoolforgeneticallyguidedpersonalizedmedicineinlynchsyndrome AT idosgregorye mylynchapatientfacingclinicaldecisionsupporttoolforgeneticallyguidedpersonalizedmedicineinlynchsyndrome AT parmigianigiovanni mylynchapatientfacingclinicaldecisionsupporttoolforgeneticallyguidedpersonalizedmedicineinlynchsyndrome AT yurgelunmatthewb mylynchapatientfacingclinicaldecisionsupporttoolforgeneticallyguidedpersonalizedmedicineinlynchsyndrome AT braundanielle mylynchapatientfacingclinicaldecisionsupporttoolforgeneticallyguidedpersonalizedmedicineinlynchsyndrome |