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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...

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Autores principales: 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
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
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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.
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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
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