Personalising monitoring for chemotherapy patients through predicting deterioration in renal and hepatic function.


Journal

Cancer medicine
ISSN: 2045-7634
Titre abrégé: Cancer Med
Pays: United States
ID NLM: 101595310

Informations de publication

Date de publication:
09 2023
Historique:
received: 22 05 2023
accepted: 26 07 2023
medline: 4 10 2023
pubmed: 23 8 2023
entrez: 23 8 2023
Statut: ppublish

Résumé

In those receiving chemotherapy, renal and hepatic dysfunction can increase the risk of toxicity and should therefore be monitored. We aimed to develop a machine learning model to identify those patients that need closer monitoring, enabling a safer and more efficient service. We used retrospective data from a large academic hospital, for patients treated with chemotherapy for breast cancer, colorectal cancer and diffuse-large B-cell lymphoma, to train and validate a Multi-Layer Perceptrons (MLP) model to predict the outcomes of unacceptable rises in bilirubin or creatinine. To assess the performance of the model, validation was performed using patient data from a separate, independent hospital using the same variables. Using this dataset, we evaluated the sensitivity and specificity of the model. 1214 patients in total were identified. The training set had almost perfect sensitivity and specificity of >0.95; the area under the curve (AUC) was 0.99 (95% CI 0.98-1.00) for creatinine and 0.97 (95% CI: 0.95-0.99) for bilirubin. The validation set had good sensitivity (creatinine: 0.60, 95% CI: 0.55-0.64, bilirubin: 0.54, 95% CI: 0.52-0.56), and specificity (creatinine 0.98, 95% CI: 0.96-0.99, bilirubin 0.90, 95% CI: 0.87-0.94) and area under the curve (creatinine: 0.76, 95% CI: 0.70, 0.82, bilirubin 0.72, 95% CI: 0.68-0.76). We have demonstrated that a MLP model can be used to reduce the number of blood tests required for some patients at low risk of organ dysfunction, whilst improving safety for others at high risk.

Sections du résumé

BACKGROUND
In those receiving chemotherapy, renal and hepatic dysfunction can increase the risk of toxicity and should therefore be monitored. We aimed to develop a machine learning model to identify those patients that need closer monitoring, enabling a safer and more efficient service.
METHODS
We used retrospective data from a large academic hospital, for patients treated with chemotherapy for breast cancer, colorectal cancer and diffuse-large B-cell lymphoma, to train and validate a Multi-Layer Perceptrons (MLP) model to predict the outcomes of unacceptable rises in bilirubin or creatinine. To assess the performance of the model, validation was performed using patient data from a separate, independent hospital using the same variables. Using this dataset, we evaluated the sensitivity and specificity of the model.
RESULTS
1214 patients in total were identified. The training set had almost perfect sensitivity and specificity of >0.95; the area under the curve (AUC) was 0.99 (95% CI 0.98-1.00) for creatinine and 0.97 (95% CI: 0.95-0.99) for bilirubin. The validation set had good sensitivity (creatinine: 0.60, 95% CI: 0.55-0.64, bilirubin: 0.54, 95% CI: 0.52-0.56), and specificity (creatinine 0.98, 95% CI: 0.96-0.99, bilirubin 0.90, 95% CI: 0.87-0.94) and area under the curve (creatinine: 0.76, 95% CI: 0.70, 0.82, bilirubin 0.72, 95% CI: 0.68-0.76).
CONCLUSIONS
We have demonstrated that a MLP model can be used to reduce the number of blood tests required for some patients at low risk of organ dysfunction, whilst improving safety for others at high risk.

Identifiants

pubmed: 37610318
doi: 10.1002/cam4.6418
pmc: PMC10524043
doi:

Substances chimiques

Creatinine AYI8EX34EU
Bilirubin RFM9X3LJ49

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

17856-17865

Informations de copyright

© 2023 The Authors. Cancer Medicine published by John Wiley & Sons Ltd.

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Auteurs

Pinkie Chambers (P)

UCL School of Pharmacy, London, UK.
Cancer Division, University College London Hospitals NHS Foundation Trust, London, UK.

Matthew Watson (M)

Department of Computer Science, Durham University, Durham, UK.

John Bridgewater (J)

Cancer Division, University College London Hospitals NHS Foundation Trust, London, UK.
UCL Cancer Institute, London, UK.

Martin D Forster (MD)

Cancer Division, University College London Hospitals NHS Foundation Trust, London, UK.
UCL Cancer Institute, London, UK.

Rebecca Roylance (R)

Cancer Division, University College London Hospitals NHS Foundation Trust, London, UK.
UCL Cancer Institute, London, UK.

Rebecca Burgoyne (R)

Cancer Division, University College London Hospitals NHS Foundation Trust, London, UK.
UCL Cancer Institute, London, UK.

Sebastian Masento (S)

Cancer Division, University College London Hospitals NHS Foundation Trust, London, UK.

Luke Steventon (L)

UCL School of Pharmacy, London, UK.
Cancer Division, University College London Hospitals NHS Foundation Trust, London, UK.

James Harmsworth King (J)

Evergreen Life, Manchester, UK.

Nick Duncan (N)

University Hospitals Birmingham NHS Foundation Trust, Birmingham, UK.

Noura Al Moubayed (N)

Department of Computer Science, Durham University, Durham, UK.

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