Evidence map›Paper›PMID 41098208›Full record

ArticleF1000Research2024

Prognostic significance of tumor budding in pancreatic carcinoma: Digitalized image approach evaluation using artificial intelligence.

Sarra Ben Rejeb, Jasser Yaacoubi

Abstract readMulticenter Study
In one paragraph

Article in F1000Research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

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3citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

2 authors.

Sarra Ben RejebPathology, Security Forces hospital Tunisia, Tunis, Tunisia.ORCID https://orcid.org/0000-0001-9150-3444
Jasser YaacoubiPathology, Security Forces hospital Tunisia, Tunis, Tunisia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Pancreatic carcinoma (PC) is a highly malignant and lethal tumor characterized by a dismal prognosis which raised the need to identify other prognostic factors for better patient risk stratification. Tumor budding (TB), defined as isolated single cancer cells or small clusters of up to four cells at the invasive front, is an emerging histoprognostic factor associated with aggressiveness in various malignancies. This study investigated the prognostic significance of tumor budding (TB) in pancreatic carcinoma using artificial intelligence. Methods: In this retrospective multicenter study, we collected all cases of PC diagnosed (2008-2022). TB was assed using 2 methods: manual on hematoxylin-eosin (HE) slides and semi-automated using QUPATH software. The selected slide for each case was digitalized using NIS software version 4.00 connected to the microscope NIKON (Eclipse Ni-U). The pathological images were then incorporated into QUPATH. The budds were counted using cell count functionality based on the nucleus size and pixel variability, and TB scores were categorized as BUDD1(0-4), BUDD2(5-9) and BUDD3(≥10). We analyzed the association between the TB score and prognostic clinicopathological factors and overall survival. Results: 25 patients were included (mean age:62.3years;male-to-female ratio:2.57). TB was found in 100%of cases and a high TB score (BUDD2-3) was observed in 56%of cases (using QUPATH versus 48% using HE slides); statistical analysis showed no significant difference between the two methods (p=0.589). A high TB score was associated with older age (>72 years), ductal histological subtype and advanced stage (pT>2).53.8% of patients with lymph node metastasis or advanced stage had high TB score. Multivariate analysis revealed that TB score was strongly and independently associated with overall survival (OS), with a hazard ratio of 2.35. Conclusion: TB is an additional prognostic factor in PC, and using artificial intelligence via QUPATH software offers a promising and accessible tool for pathologists to evaluate TB and to improve risk stratification in patients with PC.

Indexed as

Artificial IntelligenceImage Processing, Computer-AssistedPancreatic NeoplasmsAgedFemaleHumansMaleMiddle AgedPrognosisRetrospective Studiesartificial intelligence.overall survivor (OS)Pancreatic cancer (PC)prognosistumor budding (TB)

Identifiers

PMID41098208
PMCPMC12519071

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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.