Evidence map›Paper›PMID 40128853›Full record

ArticleRespiratory research2025

Mediastinal staging lymph node probability map in non-small cell lung cancer.

J Bordas-Martinez, J L Vercher-Conejero, G Rodriguez-González, P C Notta, C Martin Cabeza, N Cubero, R M Lopez-Lisbona, M Diez-Ferrer, C Tebé, S Santos and 2 more

Abstract read
In one paragraph

Article in Respiratory research, 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

12 authors.

J Bordas-MartinezPulmonology Department, Hospital General de Granollers, Barcelona, Catalonia, Spain.
J L Vercher-ConejeroNuclear Medicine Department - PET-CT, ICS-IDI, UB, Bellvitge Universitary Hospital, IDIBELL, Barcelona, Catalonia, Spain.
G Rodriguez-GonzálezPulmonology Department, Hospital General de Granollers, Barcelona, Catalonia, Spain.
P C NottaNuclear Medicine Department - PET-CT, ICS-IDI, UB, Bellvitge Universitary Hospital, IDIBELL, Barcelona, Catalonia, Spain.
C Martin CabezaPulmonology Department, Hospital General de Granollers, Barcelona, Catalonia, Spain.
N CuberoPulmonology Department, Hospital Clínico Universitario de Valladolid, Valladolid, Spain.
R M Lopez-LisbonaPulmonology Department, Bellvitge Universitary Hospital, UB, IDIBELL, CIBERES, Barcelona, Catalonia, Spain.
M Diez-FerrerPulmonology Department, Bellvitge Universitary Hospital, UB, IDIBELL, CIBERES, Barcelona, Catalonia, Spain.
C TebéBiostatistics Unit, Germans Trias i Pujol University Hospital, IGTP, Barcelona, Catalonia, Spain.
S SantosPulmonology Department, Bellvitge Universitary Hospital, UB, IDIBELL, CIBERES, Barcelona, Catalonia, Spain.
M Cortes-RomeraPulmonology Department, Hospital General de Granollers, Barcelona, Catalonia, Spain.
A RosellThorax Institute, Germans Trias i Pujol University Hospital, IGTP, UAB, Barcelona, Catalonia, Spain. arosellg.germanstrias@gencat.cat.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMediastinal lymph node (LN) staging is routinely performed using PET/CT and EBUS-TBNA. Promising predictive algorithms for lymph nodes have been reported for each technique, both individually and in combination. This study aims to develop a predictive algorithm that combines EBUS, PET/CT and clinical data to provide a probability of malignancy.

methodsA retrospective study was conducted on consecutive patients with non-small cell lung carcinoma staged using PET/CT and EBUS-TBNA. Lymph nodes were identified by level (N1, N2, and N3) and anatomical region (AR) (subcarinal, paratracheal, and hilar). A Standardized Uptake Value (SUV) was determined for each sampled LN. The ultrasound features collected included diameter in the short axis (DSA), morphology, border, echogenicity and the presence of the vascular hilum. A robust logistic regression model was used to construct an algorithm to estimate the probability of malignancy of the lymph node.

resultsA total of 116 patients with a mean age of 66, 93% of whom were men, were included. 358 lymph nodes were evaluated, 51% of which exhibited adenocarcinoma and 35% were squamous, while 14% were classified as non-small-cell lung carcinoma. The model estimated the probability of malignancy for each lymph node using age, DSA, SUVmax, and AR. The Area Under the ROC curve, was 0.89. A user-friendly application was also developed ( https://ubidi.shinyapps.io/lymma/ .)

conclusionsThe integration of patient clinical characteristics, EBUS features, and PET/CT findings may generate a pre-sampling malignancy probability map for each lymph node. The model requires prospective and external validation.

Indexed as

Carcinoma, Non-Small-Cell LungLung NeoplasmsLymph NodesMediastinumPositron Emission Tomography Computed TomographyAgedAged, 80 and overEndoscopic Ultrasound-Guided Fine Needle AspirationFemaleHumansLymphatic MetastasisMaleMiddle AgedNeoplasm StagingProbabilityRetrospective StudiesEBUSLung cancerLymph nodeMediastinal stagingPET/CT

Identifiers

PMID40128853
PMCPMC11934462

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.