Evidence map›Paper›PMID 38771787›Full record

ArticlePloS one2024

Automatic quantification of tumor-stroma ratio as a prognostic marker for pancreatic cancer.

Pierpaolo Vendittelli, John-Melle Bokhorst, Esther M M Smeets, Valentyna Kryklyva, Lodewijk A A Brosens, Caroline Verbeke, Geert Litjens

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Article in PloS one, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

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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

Who cites it

8 citing papers in PubMed.

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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

7 authors.

Pierpaolo VendittelliDepartment of Pathology, Radboud University Medical Center, Nijmegen, The Netherlands.ORCID 0000-0001-6712-3708
John-Melle BokhorstDepartment of Pathology, Radboud University Medical Center, Nijmegen, The Netherlands.
Esther M M SmeetsDepartment of Pathology, Radboud University Medical Center, Nijmegen, The Netherlands.
Valentyna KryklyvaDepartment of Pathology, Radboud University Medical Center, Nijmegen, The Netherlands.
Lodewijk A A BrosensDepartment of Pathology, Radboud University Medical Center, Nijmegen, The Netherlands.
Caroline VerbekeDepartment of Pathology, Oslo University Hospital, Oslo, Norway.
Geert LitjensDepartment of Pathology, Radboud University Medical Center, Nijmegen, The Netherlands.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThis study aims to introduce an innovative multi-step pipeline for automatic tumor-stroma ratio (TSR) quantification as a potential prognostic marker for pancreatic cancer, addressing the limitations of existing staging systems and the lack of commonly used prognostic biomarkers.

methodsThe proposed approach involves a deep-learning-based method for the automatic segmentation of tumor epithelial cells, tumor bulk, and stroma from whole-slide images (WSIs). Models were trained using five-fold cross-validation and evaluated on an independent external test set. TSR was computed based on the segmented components. Additionally, TSR's predictive value for six-month survival on the independent external dataset was assessed.

resultsMedian Dice (inter-quartile range (IQR)) of 0.751(0.15) and 0.726(0.25) for tumor epithelium segmentation on internal and external test sets, respectively. Median Dice of 0.76(0.11) and 0.863(0.17) for tumor bulk segmentation on internal and external test sets, respectively. TSR was evaluated as an independent prognostic marker, demonstrating a cross-validation AUC of 0.61±0.12 for predicting six-month survival on the external dataset.

conclusionOur pipeline for automatic TSR quantification offers promising potential as a prognostic marker for pancreatic cancer. The results underscore the feasibility of computational biomarker discovery in enhancing patient outcome prediction, thus contributing to personalized patient management.

Indexed as

Biomarkers, TumorPancreatic NeoplasmsAgedDeep LearningFemaleHumansImage Processing, Computer-AssistedMaleMiddle AgedPrognosisStromal CellsBiomarkers, Tumor

Identifiers

PMID38771787
PMCPMC11108171

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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.