Evidence map›Paper›PMID 41079022›Full record

ArticleEClinicalMedicine2025

Oesophageal cancer multi-disciplinary tool: a co-designed, externally validated, machine learning tool for oesophageal cancer decision making.

Navamayooran Thavanesan, Mohammad Naiseh, Miguel Terol, Saqib Andrew Rahman, Samuel Luke Hill, Charlotte Parfitt, Zoë S Walters, Sarvapali Ramchurn, Sheraz Markar, Richard Owen and 7 more

Abstract read
In one paragraph

Article in EClinicalMedicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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

17 authors.

Navamayooran ThavanesanInnovation for Translation Research Group (ITRG), School of Cancer Sciences, Faculty of Medicine, University of Southampton, United Kingdom.
Mohammad NaisehDepartment of Computing and Informatics, Bournemouth University, United Kingdom.
Miguel TerolInnovation for Translation Research Group (ITRG), School of Cancer Sciences, Faculty of Medicine, University of Southampton, United Kingdom.
Saqib Andrew RahmanInnovation for Translation Research Group (ITRG), School of Cancer Sciences, Faculty of Medicine, University of Southampton, United Kingdom.
Samuel Luke HillInnovation for Translation Research Group (ITRG), School of Cancer Sciences, Faculty of Medicine, University of Southampton, United Kingdom.
Charlotte ParfittUniversity Hospitals Southampton NHS Foundation Trust, United Kingdom.
Zoë S WaltersInnovation for Translation Research Group (ITRG), School of Cancer Sciences, Faculty of Medicine, University of Southampton, United Kingdom.
Sarvapali RamchurnSchool of Electronics and Computer Science, University of Southampton, United Kingdom.
Sheraz MarkarNuffield Department of Surgical Sciences, University of Oxford, United Kingdom.
Richard OwenNuffield Department of Surgical Sciences, University of Oxford, United Kingdom.
Nick MaynardNuffield Department of Surgical Sciences, University of Oxford, United Kingdom.
Tayyaba AzimSchool of Electronics and Computer Science, University of Southampton, United Kingdom.
Zehor BelkatirSchool of Electronics and Computer Science, University of Southampton, United Kingdom.
Elvira Vallejos PerezSchool of Computer Science, Horizon Digital Economy Research, University of Nottingham, United Kingdom.
Mimi McCordHeartburn Cancer UK, United Kingdom.
Tim UnderwoodInnovation for Translation Research Group (ITRG), School of Cancer Sciences, Faculty of Medicine, University of Southampton, United Kingdom.
Ganesh VigneswaranInnovation for Translation Research Group (ITRG), School of Cancer Sciences, Faculty of Medicine, University of Southampton, United Kingdom.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The oesophageal cancer (OC) multi-disciplinary team (MDT) operates under significant pressures, handling complex decision-making. Machine learning (ML) can learn complex decision-making paradigms to improve efficiency, consistency, and cost if trained and deployed responsibly. We present an externally validated ML-based clinical decision support system (CDSS) designed to predict OC MDT treatment decisions and prognosticate palliative scenarios, co-designed using Responsible Research and Innovation (RRI) principles. Methods: Clinicopathological data collected from 1931 patients between 4th September 2009, and 8th November 2022 were used to test and validate models trained through four ML algorithms to predict curative and palliative treatment pathways along with palliative prognosis. 953 OC cases treated at University Hospitals Southampton (UHS) were used to train ML models which were externally validated on 978 OC cases from Oxford University Hospitals (OUH). Model performance was evaluated using Area Under Curve (AUC) for treatment classifiers and calibration curves for survival models. A parallel RRI program at the University of Southampton (United Kingdom) combining clinician interviews and inter-disciplinary workshops was conducted between 16.3.23 and 23.5.24. The RRI program comprised a group of 17 domain experts comprising programmers, computer scientists, clinicians and patient representatives to allow end-users to contribute towards the co-design of the CDSS user interface. Findings: Cohorts differed in baseline characteristics, with the external cohort (OUH) being younger, having better performance status, and a higher prevalence of pulmonary and vascular disease. Despite these differences, on internal validation (UHS cohort) mean AUCs for the primary treatment model were: MLR 0.905 ± 0.048, XGB 0.909 ± 0.044 and RF 0.883 ± 0.059 (k = 5 cross-validation) and MLR 0.866 (95% CI 0.866-0.867), XGB 0.863 (0.862-0.864), RF 0.863 (0.867-0.868) on bootstrapped resampling. For the palliative classifier, mean AUCs were: MLR 0.805 ± 0.096, XGB 0.815 ± 0.081 and RF 0.793 ± 0.083 (k = 5 cross-validation) and MLR 0.736 (95% CI 0.734-0.737), XGB 0.799 (0.798-0.800), RF 0.781 (0.778-0.782) on bootstrapped resampling. On external validation (OUH cohort), AUCs were MLR 0.894, XGB 0.887 and RF 0.891 for the primary treatment model and MLR 0.711, XGB 0.742 and RF 0.730 for the palliative treatment classifier. Predicted survival probability from the palliative survival model was well calibrated over the first 12 months post-diagnosis in both cohorts. The RRI program provided a collaborative environment leading to valuable modifications to the CDSS including prediction explanations, visual aids for survival and integrated education for users producing a user-friendly and quick to use tool. Interpretation: We present a novel, responsibly developed, externally validated AI CDSS trained to predict oesophageal cancer MDT decisions. It represents the foundations of a transformative application of ML, personalised, consistent and efficient MDT decision-support within OC which aligns to RRI principles. Funding: Doctoral Studentship for NT (Institute for Life Sciences (University of Southampton) & University Hospital Southampton), UKRI TAS Pump-Priming Grant (TAS_PP_00167).

Indexed as

Artificial intelligenceDecision support toolMachine learningMDTMultidisciplinary teamsOesophageal cancer

Identifiers

PMID41079022
PMCPMC12513115

What OpenQuestion holds

Textmetadata
LicenceCC BY
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Registered trials

None linked

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.