Evidence map›Paper›PMID 38687915›Full record

ArticleJCO clinical cancer informatics2024

Identification and Characterization of Immune Checkpoint Inhibitor-Induced Toxicities From Electronic Health Records Using Natural Language Processing.

Hannah Barman, Sriram Venkateswaran, Antonio Del Santo, Unice Yoo, Eli Silvert, Krishna Rao, Bharathwaj Raghunathan, Lisa A Kottschade, Matthew S Block, G Scott Chandler and 3 more

Abstract read
In one paragraph

Article in JCO clinical cancer informatics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing 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

18 citing papers in PubMed.

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  18. Therapeutic Vaccination in Lung Cancer: Past Attempts, Current Approaches and Future Promises.Journal of respiratory biology and translational medicine · 2025
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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

13 authors.

Hannah Barmannference, Cambridge, MA.ORCID 0009-0008-4685-0680
Sriram VenkateswaranF. Hoffmann-La Roche, Basel, Switzerland.
Antonio Del SantoF. Hoffmann-La Roche, Basel, Switzerland.ORCID 0009-0003-7099-7862
Unice Yoonference, Cambridge, MA.
Eli Silvertnference, Cambridge, MA.ORCID 0000-0003-0445-4395
Krishna Raonference, Cambridge, MA.
Bharathwaj Raghunathannference, Cambridge, MA.
Lisa A KottschadeDepartment of Oncology, Mayo Clinic, Rochester, MN.ORCID 0000-0001-8922-2619
Matthew S BlockDepartment of Oncology, Mayo Clinic, Rochester, MN.ORCID 0000-0001-5692-4219
G Scott ChandlerF. Hoffmann-La Roche, Basel, Switzerland.ORCID 0000-0001-5339-9906
Joshua Zalisnference, Cambridge, MA.
Tyler E Wagnernference, Cambridge, MA.ORCID 0000-0001-7347-8708
Rajat MohindraF. Hoffmann-La Roche, Basel, Switzerland.ORCID 0009-0000-4233-5210

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeImmune checkpoint inhibitors (ICIs) have revolutionized cancer treatment, yet their use is associated with immune-related adverse events (irAEs). Estimating the prevalence and patient impact of these irAEs in the real-world data setting is critical for characterizing the benefit/risk profile of ICI therapies beyond the clinical trial population. Diagnosis codes, such as International Classification of Diseases codes, do not comprehensively illustrate a patient's care journey and offer no insight into drug-irAE causality. This study aims to capture the relationship between ICIs and irAEs more accurately by using augmented curation (AC), a natural language processing-based innovation, on unstructured data in electronic health records.

methodsIn a cohort of 9,290 patients treated with ICIs at Mayo Clinic from 2005 to 2021, we compared the prevalence of irAEs using diagnosis codes and AC models, which classify drug-irAE pairs in clinical notes with implied textual causality. Four illustrative irAEs with high patient impact-myocarditis, encephalitis, pneumonitis, and severe cutaneous adverse reactions, abbreviated as MEPS-were analyzed using corticosteroid administration and ICI discontinuation as proxies of severity.

resultsFor MEPS, only 70% (n = 118) of patients found by AC were also identified by diagnosis codes. Using AC models, patients with MEPS received corticosteroids for their respective irAE 82% of the time and permanently discontinued the ICI because of the irAE 35.9% (n = 115) of the time.

conclusionOverall, AC models enabled more accurate identification and assessment of patient impact of ICI-induced irAEs not found using diagnosis codes, demonstrating a novel and more efficient strategy to assess real-world clinical outcomes in patients treated with ICIs.

Indexed as

Drug-Related Side Effects and Adverse ReactionsElectronic Health RecordsImmune Checkpoint InhibitorsNatural Language ProcessingAgedFemaleHumansMaleMiddle AgedNeoplasmsImmune Checkpoint Inhibitors

Identifiers

PMID38687915
PMCPMC11161244

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Registered trials

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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.