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
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.

Identifiants

pubmed: 35308914
pii: 3574343
pmc: PMC8861666

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

641-650

Subventions

Organisme : NLM NIH HHS
ID : R56 LM013365
Pays : United States

Informations de copyright

©2021 AMIA - All rights reserved.

Références

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pubmed: 26000024

Auteurs

Grace Y E Kim (GYE)

Department of Computer Science, Stanford, CA.

Morteza Noshad (M)

Stanford Center for Biomedical Informatics Research, Stanford, CA.

Henning Stehr (H)

Department of Pathology, Stanford, CA.

Rebecca Rojansky (R)

Department of Pathology, Stanford, CA.

Dita Gratzinger (D)

Department of Pathology, Stanford, CA.

Jean Oak (J)

Department of Pathology, Stanford, CA.

Rondeep Brar (R)

Department of Hematology, Stanford, CA.

David Iberri (D)

Department of Hematology, Stanford, CA.

Christina Kong (C)

Department of Pathology, Stanford, CA.

James Zehnder (J)

Department of Pathology, Stanford, CA.
Department of Hematology, Stanford, CA.

Jonathan H Chen (JH)

Stanford Center for Biomedical Informatics Research, Stanford, CA.
Division of Hospital Medicine, Stanford, CA.

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Classifications MeSH