Evidence map›Paper›PMID 40249880›Full record

ArticleJCO clinical cancer informatics2025

Decoding Recurrence in Early-Stage and Locoregionally Advanced Non-Small Cell Lung Cancer: Insights From Electronic Health Records and Natural Language Processing.

Kyeryoung Lee, Zongzhi Liu, Qing Huang, David Corrigan, Iftekhar Kalsekar, Tomi Jun, Gustavo Stolovitzky, William K Oh, Ravi Rajaram, Xiaoyan Wang

Abstract read
In one paragraph

Article in JCO clinical cancer informatics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Article
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

10 authors.

Kyeryoung LeeGeneDx (Sema4), Stamford, CT.ORCID 0000-0002-6937-9931
Zongzhi LiuGeneDx (Sema4), Stamford, CT.ORCID 0000-0003-1578-9967
Qing HuangLung Cancer Initiative, Johnson & Johnson, New Brunswick, NJ.ORCID 0000-0001-6441-7591
David CorriganGeneDx (Sema4), Stamford, CT.ORCID 0000-0002-8239-129X
Iftekhar KalsekarLung Cancer Initiative, Johnson & Johnson, New Brunswick, NJ.ORCID 0000-0001-5232-5972
Tomi JunGeneDx (Sema4), Stamford, CT.ORCID 0000-0002-2120-1704
Gustavo StolovitzkyGeneDx (Sema4), Stamford, CT.ORCID 0000-0002-9618-2819
William K OhGeneDx (Sema4), Stamford, CT.ORCID 0000-0001-5113-8147
Ravi RajaramDepartment of Thoracic and Cardiovascular Surgery, The University of Texas MD Anderson Cancer Center, Houston, TX.
Xiaoyan WangGeneDx (Sema4), Stamford, CT.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeRecurrences after curative resection in early-stage and locoregionally advanced non-small cell lung cancer (NSCLC) are common, necessitating a nuanced understanding of associated risk factors. This study aimed to establish a natural language processing (NLP) system to efficiently curate recurrence data in NSCLC and analyze risk factors longitudinally. PATIENTS AND

methodsElectronic health records of 6,351 patients with NSCLC with >700,000 notes were obtained from Mount Sinai's data sets. A deep learning-based customized NLP system was developed to identify cohorts experiencing recurrence. Recurrence types and rates over time were stratified by various clinical features. Cohort description analysis, Kaplan-Meier analysis for overall recurrence-free survival (RFS) and distant metastasis-free survival (DMFS), and Cox proportional hazards analysis were performed.

resultsOf 1,295 patients with stage I-IIIA NSCLC with surgical resections, 336 patients (25.9%) experienced recurrence, as identified through NLP. The NLP system achieved a precision of 94.3%, a recall of 93%, and an F1 score of 93.5. Among 336 patients, 52.4% had local/regional recurrences, 44% distant metastases, and 3.6% unknown recurrence. RFS rates at years 1-5 were 93%, 81%, 73%, 67%, and 61%, respectively (96%, 89%, 84%, 80%, and 75% for distant metastasis). Stage-specific RFS rates at year 5 were 73% (IA), 62% (IB), 47% (IIA), 46% (IIB), and 20% (IIIA). Stage IB patients had a significantly higher likelihood of recurrence versus stage IA (adjusted hazard ratio [aHR], 1.63;

conclusionOur scalable NLP system enabled us to generate real-world insights into NSCLC recurrences, paving the way for predictive models for preventing, diagnosing, and treating NSCLC recurrence.

Indexed as

Carcinoma, Non-Small-Cell LungElectronic Health RecordsLung NeoplasmsNatural Language ProcessingNeoplasm Recurrence, LocalAgedDeep LearningFemaleHumansMaleMiddle AgedNeoplasm StagingPrognosisRisk Factors

Identifiers

PMID40249880
PMCPMC12011440

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.