Evidence map›Paper›PMID 41865337›Full record

ArticleClinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico2026

Stable or not? unraveling the reliability of radiomic features in 4d-computed tomography in early-stage non-small cell lung cancer.

Stefania Volpe, Aurora Gaeta, Maria Giulia Vincini, Mattia Zaffaroni, Federico Mastroleo, Sara Raimondi, Matteo Pepa, Lars Johannes Isaksson, Marta Cremonesi, Davide La Torre and 5 more

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Article in Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico, 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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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

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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

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4 · The record

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5 · Who and what money

Authors and funding

15 authors.

Stefania VolpeDivision of Radiation Oncology, IEO European Institute of Oncology IRCCS, Milan, Italy.
Aurora GaetaDepartment of Experimental Oncology Molecular and Pharmaco-Epidemiology Unit, IEO, European Institute of Oncology IRCCS, Milan, Italy.
Maria Giulia VinciniDivision of Radiation Oncology, IEO European Institute of Oncology IRCCS, Milan, Italy. mariagiulia.vincini@ieo.it.ORCID http://orcid.org/0000-0001-7830-3149
Mattia Zaffaroni *Division of Radiation Oncology, IEO European Institute of Oncology IRCCS, Milan, Italy. mattia.zaffaroni@ieo.it.
Federico MastroleoDivision of Radiation Oncology, IEO European Institute of Oncology IRCCS, Milan, Italy.
Sara RaimondiDepartment of Experimental Oncology Molecular and Pharmaco-Epidemiology Unit, IEO, European Institute of Oncology IRCCS, Milan, Italy.
Matteo PepaDivision of Radiation Oncology, IEO European Institute of Oncology IRCCS, Milan, Italy.
Lars Johannes Isaksson *Division of Radiation Oncology, IEO European Institute of Oncology IRCCS, Milan, Italy.
Marta CremonesiUnit of Radiation Research, IEO, European Institute of Oncology IRCCS, Milan, Italy.
Davide La TorreDepartment of Oncology and Hemato-Oncology, University of Milan, Milan, Italy.
Matthias GuckenbergerDepartment of Radiation Oncology, University Hospital Zurich and University of Zurich, Zurich, Switzerland.
Federica BellerbaDepartment of Experimental Oncology Molecular and Pharmaco-Epidemiology Unit, IEO, European Institute of Oncology IRCCS, Milan, Italy.
Roberto OrecchiaScientific Directorate, IEO European Institute of Oncology IRCCS, Milan, Italy.
Sara Gandini *Department of Experimental Oncology, IEO European Institute of Oncology IRCCS, Milan, Italy.
Barbara Alicja Jereczek-FossaDivision of Radiation Oncology, IEO European Institute of Oncology IRCCS, Milan, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimFour-dimensional computed tomography (4D-CT) is the gold standard for radiotherapy planning in non-small cell lung cancer (NSCLC), yet its use in radiomics remains underexplored. This study proposes a reproducible, scalable methodology for assessing radiomic feature (RF) stability in 4D-CT and evaluates whether image filtering identifies additional stable RFs compared to unfiltered images.

methodsEarly-stage NSCLC patients treated with SBRT with 4D-CT were included. Gross tumor volumes (GTVs) were re-segmented on all available phases. RFs were extracted using PyRadiomics. Features with near-zero variance in > 85% of patients were excluded. RF stability was evaluated using two complementary approaches: (i) coefficient of variation (COV), quantifying the magnitude of inter-phase variability, and (ii) repeated-measures modeling, assessing the presence of a statistically significant association between RF values and respiratory phase. RFs with COV < 5% and 5-10% were considered highly stable and stable, respectively. Repeated-measures analyses were performed separately for expiratory (0-40%) and inspiratory (50-90%) phases.

resultsSeventy patients met the inclusion criteria. 1892 RFs were analyzable. Based on COV, about 21% (397/1892) of RFs were highly stable, and 18% (338/1892) were stable, while the remaining showed intermediate or high variability. The largest proportion of highly stable RFs derived from lbp-3D (25%) and log-sigma (12%) filtered images. Repeated measures analysis showed that only a limited subset of RFs had a statistically-significant dependence on respiratory phase, with 1747 and 1744 RFs remaining time-independent across expiratory and inspiratory phases, respectively.

conclusionRadiomic features extracted from 4D-CT images in early-stage NSCLC patients show heterogeneous stability across respiratory phases. Radiomic features extracted from 4D-CT images in early-stage NSCLC exhibit heterogeneous quantitative variability across respiratory phases. However, only a minority of features show statistically significant time dependence. The study provides a reproducible methodological framework to identify stable radiomic features from 4D-CT, enabling their more reliable use in lung cancer radiomic studies.

Indexed as

Carcinoma, Non-Small-Cell LungFour-Dimensional Computed TomographyLung NeoplasmsRadiomicsRadiotherapy Planning, Computer-AssistedAgedFemaleHumansMaleMiddle AgedNeoplasm StagingRadiosurgeryReproducibility of ResultsEarly-stage non-small cell lung cancerFeature stabilityRadiomicsSBRT

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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.