Evidence map›Paper›PMID 40703809›Full record

ArticleNeuro-oncology advances

Natural language processing algorithms identify wild-type isocitrate dehydrogenase gliomas in electronic health records.

Noah Forrest, Vijeeth Guggilla, April Bell, Susan Zelisko, Emma M Federico, Erica A Power, Steven Birch, Khizar R Nandoliya, Ethan J Houskamp, Steven Tran and 5 more

Abstract read
In one paragraph

Article in Neuro-oncology advances. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

15 authors.

Noah ForrestInstitute for Artificial Intelligence in Medicine, Feinberg School of Medicine, Northwestern University, Chicago, Illinois, USA.ORCID https://orcid.org/0000-0003-4601-7070
Vijeeth GuggillaInstitute for Artificial Intelligence in Medicine, Feinberg School of Medicine, Northwestern University, Chicago, Illinois, USA.ORCID https://orcid.org/0000-0001-9132-514X
April BellInstitute for Artificial Intelligence in Medicine, Feinberg School of Medicine, Northwestern University, Chicago, Illinois, USA.ORCID https://orcid.org/0000-0001-6268-0126
Susan ZeliskoInformatics and Systems Development, Health Sciences Division, Loyola University Chicago, Maywood, Illinois, USA.
Emma M FedericoDepartment of Cancer Biology, Stritch School of Medicine, Loyola University Chicago, Maywood, Illinois, USA.ORCID https://orcid.org/0000-0002-6537-2046
Erica A PowerDepartment of Cancer Biology, Stritch School of Medicine, Loyola University Chicago, Maywood, Illinois, USA.ORCID https://orcid.org/0000-0001-6535-4510
Steven BirchInformatics and Systems Development, Health Sciences Division, Loyola University Chicago, Maywood, Illinois, USA.
Khizar R NandoliyaFeinberg School of Medicine, Northwestern University, Chicago, Illinois, USA.ORCID https://orcid.org/0000-0002-6616-4388
Ethan J HouskampFeinberg School of Medicine, Northwestern University, Chicago, Illinois, USA.ORCID https://orcid.org/0000-0002-2090-562X
Steven TranInstitute for Artificial Intelligence in Medicine, Feinberg School of Medicine, Northwestern University, Chicago, Illinois, USA.ORCID https://orcid.org/0000-0001-7273-2348
Rimas V LukasDepartment of Neurology, Feinberg School of Medicine, Northwestern University, Chicago, Illinois, USA.ORCID https://orcid.org/0000-0002-9352-5396
Jodi L JohnsonRobert H. Lurie Comprehensive Cancer Center, Feinberg School of Medicine, Northwestern University, Chicago, Illinois, USA.ORCID https://orcid.org/0000-0002-8328-5587
Ishan RoyRobert H. Lurie Comprehensive Cancer Center, Feinberg School of Medicine, Northwestern University, Chicago, Illinois, USA.ORCID https://orcid.org/0000-0002-9109-0421
Derek A WainwrightCardinal Bernardin Cancer Center, Loyola University Medical Center, Maywood, Illinois, USA.ORCID https://orcid.org/0000-0001-7232-4264
Theresa L WalunasRobert H. Lurie Comprehensive Cancer Center, Feinberg School of Medicine, Northwestern University, Chicago, Illinois, USA.ORCID https://orcid.org/0000-0002-7653-3650

Funding

IDO1 and Immunotolerance in GlioblastomaR01NS097851 · NINDS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI SCHILTZ, GARY E, WAINWRIGHT, DEREK ALAN · 2016 to 2025
$4.6M
Extratumoral biological determinants that decrease survival in older adults with glioblastomaR01NS129835 · NINDS · LOYOLA UNIVERSITY CHICAGO · PI Derek Alan Wainwright · 2023 to 2026
$1.5M
The interaction of IDO and Tregs Leads to Immunosuppression in GliomaR00NS082381 · NINDS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI WAINWRIGHT, DEREK ALAN · 2014 to 2016
$735k
Aging, immunosenescence and glioblastomaK02AG068617 · NIA · NORTHWESTERN UNIVERSITY AT CHICAGO · PI WAINWRIGHT, DEREK ALAN · 2020 to 2024
$688k
The interaction of IDO and Tregs Leads to Immunosuppression in GliomaK99NS082381 · NINDS · UNIVERSITY OF CHICAGO · PI WAINWRIGHT, DEREK ALAN · 2013 to 2014
$173k
The role of IDO and Th17 in an experimental mouse model of gliomaF32NS073366 · NINDS · UNIVERSITY OF CHICAGO · PI WAINWRIGHT, DEREK ALAN · 2011 to 2012
$86k
NIA NIH HHS K02 AG068617NINDS NIH HHS F32 NS073366NINDS NIH HHS K99 NS082381NINDS NIH HHS R00 NS082381NINDS NIH HHS R01 NS097851NINDS NIH HHS R01 NS129835
6 · The paper itself

Abstract

Background: In 2021, the World Health Organization reclassified glioblastomas to include only gliomas with wild-type isocitrate dehydrogenase (IDHwt). Reclassification has created a challenge for retrospective identification of patients with GBM, as many were classified with outdated definitions. This study aims to address this challenge by using natural language processing (NLP) on electronic health record (EHR) data to identify patients with wild-type IDH glioma. Methods: We manually adjudicated a subset of 1499 pathology records for evidence of IDHwt glioma as well as the methylation status of the MGMT promoter. We then trained several regularized logistic regression models that identify the IDH mutation and MGMT promoter status using biomedical concepts identified in the text. These models were then validated at a second site. Kaplan-Meier curves stratifying patients by their MGMT promoter methylation status and other clinical variables were constructed for further cohort characterization. Results: The best-performing model for identifying IDHwt glioma displayed an F1 measure of 0.88. Comparing patients with methylated and unmethylated MGMT promoter showed significant differences in median overall survival times ( Discussion: Our results suggest that we can identify patients with IDHwt glioma in pathology notes in the EHR using NLP. Our models displayed excellent performance at a secondary healthcare institution, demonstrating that they can identify multi-site GBM cohorts. Furthermore, our characterization of the NM GBM cohort recapitulated known survival trends, demonstrating the utility of EHR data in studying GBM in clinical settings.

Indexed as

electronic health recordsglioblastoma naturallanguage processing

Identifiers

PMID40703809
PMCPMC12284639

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.