Evidence map›Paper›PMID 40355935›Full record

ArticleJournal of translational medicine2025

Fully volumetric body composition analysis for prognostic overall survival stratification in melanoma patients.

Katarzyna Borys, Georg Lodde, Elisabeth Livingstone, Carsten Weishaupt, Christian Römer, Marc-David Künnemann, Anne Helfen, Lisa Zimmer, Wolfgang Galetzka, Johannes Haubold and 6 more

Erratum issuedAbstract read
In one paragraph

Article in Journal of translational medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors.

Katarzyna BorysInstitute for Artificial Intelligence in Medicine, University Hospital Essen, Girardetstraße 2, 245131, Essen, Germany. katarzyna.borys@uk-essen.de.ORCID 0000-0001-6987-6041
Georg LoddeInstitute of Dermatology, University Hospital Essen, Essen, Germany.
Elisabeth LivingstoneInstitute of Dermatology, University Hospital Essen, Essen, Germany.
Carsten WeishauptDepartment of Dermatology, University Hospital Münster, Münster, Germany.
Christian RömerClinic for Radiology, University Hospital Münster, Münster, Germany.
Marc-David KünnemannClinic for Radiology, University Hospital Münster, Münster, Germany.
Anne HelfenClinic for Radiology, University Hospital Münster, Münster, Germany.
Lisa ZimmerInstitute of Dermatology, University Hospital Essen, Essen, Germany.
Wolfgang GaletzkaInstitute of Medical Informatics, Biometry and Epidemiology, University Hospital Essen, University of Duisburg-Essen, Essen, Germany.
Johannes HauboldInstitute for Artificial Intelligence in Medicine, University Hospital Essen, Girardetstraße 2, 245131, Essen, Germany.
Christoph M FriedrichInstitute of Medical Informatics, Biometry and Epidemiology, University Hospital Essen, University of Duisburg-Essen, Essen, Germany.
Lale UmutluInstitute of Diagnostic and Interventional Radiology and Neuroradiology, University Hospital Essen, Essen, Germany.
Walter HeindelClinic for Radiology, University Hospital Münster, Münster, Germany.
Dirk SchadendorfInstitute of Dermatology, University Hospital Essen, Essen, Germany.
René Hosch *Institute for Artificial Intelligence in Medicine, University Hospital Essen, Girardetstraße 2, 245131, Essen, Germany.
Felix Nensa *Institute for Artificial Intelligence in Medicine, University Hospital Essen, Girardetstraße 2, 245131, Essen, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAccurate assessment of expected survival in melanoma patients is crucial for treatment decisions. This study explores deep learning-based body composition analysis to predict overall survival (OS) using baseline Computed Tomography (CT) scans and identify fully volumetric, prognostic body composition features.

methodsA deep learning network segmented baseline abdomen and thorax CTs from a cohort of 495 patients. The Sarcopenia Index (SI), Myosteatosis Fat Index (MFI), and Visceral Fat Index (VFI) were derived and statistically assessed for prognosticating OS. External validation was performed with 428 patients.

resultsSI was significantly associated with OS on both CT regions: abdomen (P ≤ 0.0001, HR: 0.36) and thorax (P ≤ 0.0001, HR: 0.27), with lower SI associated with prolonged survival. MFI was also associated with OS on abdomen (P ≤ 0.0001, HR: 1.16) and thorax CTs (P ≤ 0.0001, HR: 1.08), where higher MFI was linked to worse outcomes. Lastly, VFI was associated with OS on abdomen CTs (P ≤ 0.001, HR: 1.90), with higher VFI linked to poor outcomes. External validation replicated these results.

conclusionsSI, MFI, and VFI showed substantial potential as prognostic factors for OS in malignant melanoma patients. This approach leveraged existing CT scans without additional procedural or financial burdens, highlighting the seamless integration of DL-based body composition analysis into standard oncologic staging routines.

Indexed as

Body CompositionCone-Beam Computed TomographyDeep LearningMelanomaAbdomenAgedCohort StudiesFemaleHumansImage Processing, Computer-AssistedIntra-Abdominal FatMaleMiddle AgedMultivariate AnalysisRegression AnalysisSarcopeniaBiomarkersBody compositionCancerComputed tomographyMelanomaOverall survivalPrognostication

Identifiers

PMID40355935
PMCPMC12067685

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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.