Evidence map›Paper›PMID 42335041›Full record

ArticlePloS one2026

Longitudinal analysis of CYFRA 21-1 levels in patients with pulmonary nodules: Differential trajectories between benign and malignant cases.

Yency J Forero, Michael N Kammer, Kevin C McGann, Hudson Holmes, Sheau-Chiann Chen, Heidi Chen, Samson Argaw, Timothy A Khalil, Sanja L Antic, Yong Zou and 6 more

Abstract read
In one paragraph

Article in PloS one, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

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0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors.

Yency J ForeroDivision of Allergy, Pulmonary and Critical Care Medicine, Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee, United States of America.ORCID https://orcid.org/0000-0003-3889-4081
Michael N KammerDivision of Allergy, Pulmonary and Critical Care Medicine, Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee, United States of America.
Kevin C McGannDepartment of Thoracic Surgery, Vanderbilt University Medical Center, Nashville, Tennessee, United States of America.ORCID https://orcid.org/0009-0005-3575-6873
Hudson HolmesDepartment of Thoracic Surgery, Vanderbilt University Medical Center, Nashville, Tennessee, United States of America.
Sheau-Chiann ChenDepartment of Biostatistics, Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee, United States of America.
Heidi ChenDepartment of Biostatistics, Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee, United States of America.
Samson ArgawDivision of Allergy, Pulmonary and Critical Care Medicine, Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee, United States of America.
Timothy A KhalilDivision of Allergy, Pulmonary and Critical Care Medicine, Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee, United States of America.ORCID https://orcid.org/0009-0009-9469-9353
Sanja L AnticDivision of Allergy, Pulmonary and Critical Care Medicine, Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee, United States of America.
Yong ZouDivision of Allergy, Pulmonary and Critical Care Medicine, Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee, United States of America.
Lianrui ZuoBiomedical Engineering, Vanderbilt University, Nashville, Tennessee, United States of America.ORCID https://orcid.org/0000-0002-5923-9097
Thomas A LaskoBiomedical Informatics, Vanderbilt University Medical Center, Nashville, Tennessee, United States of America.ORCID https://orcid.org/0000-0003-2300-9529
Bennet A LandmanBiomedical Engineering, Vanderbilt University, Nashville, Tennessee, United States of America.ORCID https://orcid.org/0000-0001-5733-2127
Stephen A DeppenDepartment of Thoracic Surgery, Vanderbilt University Medical Center, Nashville, Tennessee, United States of America.
Eric L GroganDepartment of Thoracic Surgery, Vanderbilt University Medical Center, Nashville, Tennessee, United States of America.ORCID https://orcid.org/0000-0002-3886-9399
Fabien MaldonadoDivision of Allergy, Pulmonary and Critical Care Medicine, Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee, United States of America.ORCID https://orcid.org/0000-0002-6504-2063

Funding

Validation of Biomarkers of Risk for the Early Detection of Lung CancerU01CA152662 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI DEPPEN, STEPHEN, GROGAN, ERIC L · 2010 to 2025
$12.8M
NCI NIH HHS U01 CA152662
6 · The paper itself

Abstract

backgroundCYFRA 21-1, a cytokeratin-19 fragment, is a validated serum biomarker for non-small cell lung cancer (NSCLC). However, most studies rely on single time-point measurements, limiting its specificity in differentiating malignancy from benign pulmonary conditions. Inspired by the clinical utility of serial PSA measurements in prostate cancer, we investigated whether longitudinal trends in CYFRA 21-1 could enhance diagnostic and monitoring capabilities in patients with pulmonary nodules. METHODS AND

findingsWe analyzed 132 patients with pulmonary nodules from the Vanderbilt Thoracic Biorepository. For the primary analysis, patients who underwent treatment prior to biomarker assessment were excluded, resulting in an untreated cohort of 121 patients (91 benign and 30 malignant nodules). CYFRA 21-1 levels were measured serially using electrochemiluminescence assays. Longitudinal trends were assessed using linear mixed-effects models to estimate biomarker trajectories. Primary analyses compared benign vs. malignant nodules using longitudinal modeling of log-transformed CYFRA 21-1 values. At baseline, CYFRA 21-1 levels were significantly higher in malignant versus benign nodules. Longitudinal mixed-effects modeling did not demonstrate statistically significant differences in trajectories between benign and malignant nodules. Benign nodules showed a small positive trend in log(CYFRA 21-1) whereas malignant nodules showed greater longitudinal variability. The magnitude of change assessed using the absolute slope of log(CYFRA 21-1) was significantly greater in malignant nodules compared with benign nodules (p < 0.05). Exploratory diagnostic analysis showed that baseline log(CYFRA 21-1) achieved and AUC of 0.68 (95% CI 0.56-0.79) with sensitivity 0.63 and specificity 0.71. The absolute slope of log(CYFRA 21-1) yielded an AUC of 0.67 (95% CI 0.48-0.87) with sensitivity 0.39 and specificity 0.97.

conclusionsCYFRA 21-1 exhibits substantial within-patient variability over time, with trajectories that reflect disease state and treatment. These findings suggest that longitudinal monitoring of CYFRA 21-1 may provide additional information beyond single time-point measurements in the evaluation of pulmonary nodules. Further studies in large prospective cohorts are warranted to validate these findings before clinical implementation.

Indexed as

Antigens, NeoplasmBiomarkers, TumorCarcinoma, Non-Small-Cell LungKeratin-19Lung NeoplasmsAgedDiagnosis, DifferentialFemaleHumansLongitudinal StudiesMaleMiddle Agedantigen CYFRA21.1Antigens, NeoplasmBiomarkers, TumorKeratin-19

Identifiers

PMID42335041
PMCPMC13289921

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