Machine Learning Predictability of Clinical Next Generation Sequencing for Hematologic Malignancies to Guide High-Value Precision Medicine.
Journal
AMIA ... Annual Symposium proceedings. AMIA Symposium
ISSN: 1942-597X
Titre abrégé: AMIA Annu Symp Proc
Pays: United States
ID NLM: 101209213
Informations de publication
Date de publication:
2021
2021
Historique:
entrez:
21
3
2022
pubmed:
22
3
2022
medline:
12
4
2022
Statut:
epublish
Résumé
Advancing diagnostic testing capabilities such as clinical next generation sequencing methods offer the potential to diagnose, risk stratify, and guide specialized treatment, but must be balanced against the escalating costs of healthcare to identify patient cases most likely to benefit from them. Heme-STAMP (Stanford Actionable Mutation Panel for Hematopoietic and Lymphoid Malignancies) is one such next generation sequencing test. Our objective is to assess how well Heme-STAMP pathological variants can be predicted given electronic health records data available at the time of test ordering. The model demonstrated AUROC 0.74 (95% CI: [0.72, 0.76]) with 99% negative predictive value at 6% specificity. A benchmark for comparison is the prevalence of positive results in the dataset at 58.7%. Identifying patients with very low or very high predicted probabilities of finding actionable mutations (positive result) could guide more precise high-value selection of patient cases to test.
Substances chimiques
Heme
42VZT0U6YR
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Research Support, U.S. Gov't, Non-P.H.S.
Langues
eng
Sous-ensembles de citation
IM
Pagination
641-650Subventions
Organisme : NLM NIH HHS
ID : R56 LM013365
Pays : United States
Informations de copyright
©2021 AMIA - All rights reserved.
Références
J Anal Test. 2018;2(3):249-262
pubmed: 30842888
AMIA Annu Symp Proc. 2009 Nov 14;2009:391-5
pubmed: 20351886
Genome Biol. 2011 Sep 28;12(9):R94
pubmed: 21955854
AMIA Jt Summits Transl Sci Proc. 2019 May 06;2019:315-324
pubmed: 31258984
Per Med. 2014;11(5):523-544
pubmed: 26000024