Evidence map›Paper›PMID 35133484›Full record

ArticleEuropean radiology2022

SUVmax to tumor perimeter distance: a robust radiomics prognostic biomarker in resectable non-small cell lung cancer patients.

Germán Andrés Jiménez Londoño, Ana Maria García Vicente, Jesús J Bosque, Mariano Amo-Salas, Julián Pérez-Beteta, Antonio Francisco Honguero-Martinez, Víctor M Pérez-García, Ángel María Soriano Castrejón

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In one paragraph

Article in European radiology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
2.7field-weighted citation impact, top 10% of its field
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

14 citing papers in PubMed, 1 synthesis or guideline pooled it, 21 citations in OpenAlex.

  1. Pooled it
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  9. Clinicopathologic and metabolic variables fromAnnals of nuclear medicine · 2025
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  12. Promising Candidate Prognostic Biomarkers in [Journal of nuclear medicine : official publication, Society of Nuclear Medicine · 2024
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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

8 authors at 3 institutions in 1 country.

Germán Andrés Jiménez LondoñoDepartment of Nuclear Medicine, Hospital General Universitario de Ciudad Real, Ciudad Real, Spain. gjimenez91@yahoo.com.
Ana Maria García VicenteDepartment of Nuclear Medicine, Hospital General Universitario de Ciudad Real, Ciudad Real, Spain.
Jesús J BosqueDepartment of Mathematics, Mathematical Oncology Laboratory (MOLAB), Universidad de Castilla-La Mancha, Ciudad Real, Spain.
Mariano Amo-SalasDepartment of Mathematics, Universidad de Castilla-La Mancha, Ciudad Real, Spain.
Julián Pérez-BetetaDepartment of Mathematics, Mathematical Oncology Laboratory (MOLAB), Universidad de Castilla-La Mancha, Ciudad Real, Spain.
Antonio Francisco Honguero-MartinezDepartment of Surgery, Hospital General Universitario de Albacete, Albacete, Spain.
Víctor M Pérez-GarcíaDepartment of Mathematics, Mathematical Oncology Laboratory (MOLAB), Universidad de Castilla-La Mancha, Ciudad Real, Spain.
Ángel María Soriano CastrejónDepartment of Nuclear Medicine, Hospital General Universitario de Ciudad Real, Ciudad Real, Spain.
University of Castilla-La Mancha · ESHospital General Universitario de Ciudad Real · ESHospital General Universitario de Albacete · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThe purpose of this study was to evaluate the prognostic value of novel geometric variables obtained from pre-treatment [

methodsRetrospective study including stage I-III NSCLC patients with baseline [

resultsA cohort of 173 patients was selected. ER was detected in 49/104 of patients with recurrent disease. Additionally, 100 patients died and 53 had STM. Age, pathologic lymphovascular invasion, lymph nodal infiltration, TNM stage, nSCD, and nSPD were associated with ER, although only age (aOR = 1.06, p = 0.002), pathologic lymphovascular invasion (aOR = 3.40, p = 0.022), and nSPD (aOR = 0.02, p = 0.018) were significant independent predictors of ER in multivariate analysis. Age, lymph nodal infiltration, TNM stage, nSCD, and nSPD were predictors of STM. Age (aOR = 1.05, p = 0.006), lymph nodal infiltration (aOR = 2.72, p = 0.005), and nSPD (aOR = 0.03, p = 0.022) were significantly associated with STM in multivariate analysis. Coefficient of variation (COV) and SUVmean/SUVmax ratio did not show significant predictive value with respect to ER or STM.

conclusionThe geometric variables, nSCD and nSPD, are robust biomarkers of the poorest outcome prediction of patients with NSCLC with respect to classical PET variables. KEY POINTS: • In NSCLC patients, it is crucial to find prognostic parameters since TNM system alone cannot explain the variation in lung cancer survival. • Age, lymphovascular invasion, lymph nodal infiltration, and metabolic geometrical parameters were useful as prognostic parameters. • The displacement grade of the highest point of metabolic activity towards the periphery assessed by geometric variables obtained from [

Indexed as

Carcinoma, Non-Small-Cell LungLung NeoplasmsFluorodeoxyglucose F18HumansPositron-Emission TomographyPositron Emission Tomography Computed TomographyPrognosisRadiopharmaceuticalsRetrospective StudiesFluorodeoxyglucose F18Radiopharmaceuticals[18F]FDG PET/CTGeometric variablesNon-small cell lung cancerPrognosisRadiomics

Identifiers

PMID35133484
OpenAlexW4210921791

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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.