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Development and validation of a multivariable risk factor questionnaire to detect oesophageal cancer in 2-week wait patients.
Ho, Kai Man Alexander; Rosenfeld, Avi; Hogan, Áine; McBain, Hazel; Duku, Margaret; Wolfson, Paul Bd; Wilson, Ashley; Cheung, Sharon My; Hennelly, Laura; Macabodbod, Lester; Graham, David G; Sehgal, Vinay; Banerjee, Amitava; Lovat, Laurence B.
  • Ho KMA; Division of Surgery and Interventional Science, University College London, Charles Bell House, 43-45 Foley Street, London W1W 7TY, UK; Wellcome/EPSRC Centre for Interventional and Surgical Sciences (WEISS), University College London, Charles Bell House, 43-45 Foley Street, London W1W 7TY, UK. Electr
  • Rosenfeld A; Department of Computer Science, Jerusalem College of Technology, Havaad Haleumi 21, Givat Mordechai 91160 Jerusalem, Israel.
  • Hogan Á; Division of Surgery and Interventional Science, University College London, Charles Bell House, 43-45 Foley Street, London W1W 7TY, UK.
  • McBain H; Division of Surgery and Interventional Science, University College London, Charles Bell House, 43-45 Foley Street, London W1W 7TY, UK.
  • Duku M; Division of Surgery and Interventional Science, University College London, Charles Bell House, 43-45 Foley Street, London W1W 7TY, UK.
  • Wolfson PB; Division of Surgery and Interventional Science, University College London, Charles Bell House, 43-45 Foley Street, London W1W 7TY, UK; Wellcome/EPSRC Centre for Interventional and Surgical Sciences (WEISS), University College London, Charles Bell House, 43-45 Foley Street, London W1W 7TY, UK.
  • Wilson A; Division of Surgery and Interventional Science, University College London, Charles Bell House, 43-45 Foley Street, London W1W 7TY, UK.
  • Cheung SM; Division of Surgery and Interventional Science, University College London, Charles Bell House, 43-45 Foley Street, London W1W 7TY, UK; Wellcome/EPSRC Centre for Interventional and Surgical Sciences (WEISS), University College London, Charles Bell House, 43-45 Foley Street, London W1W 7TY, UK.
  • Hennelly L; Division of Surgery and Interventional Science, University College London, Charles Bell House, 43-45 Foley Street, London W1W 7TY, UK.
  • Macabodbod L; Division of Surgery and Interventional Science, University College London, Charles Bell House, 43-45 Foley Street, London W1W 7TY, UK.
  • Graham DG; Department of Gastrointestinal Services, University College London Hospital, University College London Hospitals NHS Foundation Trust, 235 Euston Road, London NW1 2BU, UK.
  • Sehgal V; Department of Gastrointestinal Services, University College London Hospital, University College London Hospitals NHS Foundation Trust, 235 Euston Road, London NW1 2BU, UK.
  • Banerjee A; Institute of Health Informatics, University College London, 222 Euston Road, London NW1 2DA, UK; Department of Cardiology, St Bartholomew's Hospital, Barts Health NHS Trust, London EC1A 7BE, UK.
  • Lovat LB; Division of Surgery and Interventional Science, University College London, Charles Bell House, 43-45 Foley Street, London W1W 7TY, UK; Wellcome/EPSRC Centre for Interventional and Surgical Sciences (WEISS), University College London, Charles Bell House, 43-45 Foley Street, London W1W 7TY, UK; Depart
Clin Res Hepatol Gastroenterol ; 47(3): 102087, 2023 03.
Article in English | MEDLINE | ID: covidwho-2177684
ABSTRACT

INTRODUCTION:

Oesophageal cancer is associated with poor health outcomes. Upper GI (UGI) endoscopy is the gold standard for diagnosis but is associated with patient discomfort and low yield for cancer. We used a machine learning approach to create a model which predicted oesophageal cancer based on questionnaire responses.

METHODS:

We used data from 2 separate prospective cross-sectional studies the Saliva to Predict rIsk of disease using Transcriptomics and epigenetics (SPIT) study and predicting RIsk of diSease using detailed Questionnaires (RISQ) study. We recruited patients from National Health Service (NHS) suspected cancer pathways as well as patients with known cancer. We identified patient characteristics and questionnaire responses which were most associated with the development of oesophageal cancer. Using the SPIT dataset, we trained seven different machine learning models, selecting the best area under the receiver operator curve (AUC) to create our final model. We further applied a cost function to maximise cancer detection. We then independently validated the model using the RISQ dataset.

RESULTS:

807 patients were included in model training and testing, split in a 7030 ratio. 294 patients were included in model validation. The best model during training was regularised logistic regression using 17 features (median AUC 0.81, interquartile range (IQR) 0.69-0.85). For testing and validation datasets, the model achieved an AUC of 0.71 (95% CI 0.61-0.81) and 0.92 (95% CI 0.88-0.96) respectively. At a set cut off, our model achieved a sensitivity of 97.6% and specificity of 59.1%. We additionally piloted the model in 12 patients with gastric cancer; 9/12 (75%) of patients were correctly classified.

CONCLUSIONS:

We have developed and validated a risk stratification tool using a questionnaire approach. This could aid prioritising patients at high risk of having oesophageal cancer for endoscopy. Our tool could help address endoscopic backlogs caused by the COVID-19 pandemic.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Esophageal Neoplasms / COVID-19 Type of study: Cohort study / Diagnostic study / Observational study / Prognostic study / Randomized controlled trials Limits: Humans Language: English Journal: Clin Res Hepatol Gastroenterol Year: 2023 Document Type: Article

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Esophageal Neoplasms / COVID-19 Type of study: Cohort study / Diagnostic study / Observational study / Prognostic study / Randomized controlled trials Limits: Humans Language: English Journal: Clin Res Hepatol Gastroenterol Year: 2023 Document Type: Article