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Personalising monitoring for chemotherapy patients through predicting deterioration in renal and hepatic function.
Chambers, Pinkie; Watson, Matthew; Bridgewater, John; Forster, Martin D; Roylance, Rebecca; Burgoyne, Rebecca; Masento, Sebastian; Steventon, Luke; Harmsworth King, James; Duncan, Nick; Al Moubayed, Noura.
Afiliação
  • Chambers P; UCL School of Pharmacy, London, UK.
  • Watson M; Cancer Division, University College London Hospitals NHS Foundation Trust, London, UK.
  • Bridgewater J; Department of Computer Science, Durham University, Durham, UK.
  • Forster MD; Cancer Division, University College London Hospitals NHS Foundation Trust, London, UK.
  • Roylance R; UCL Cancer Institute, London, UK.
  • Burgoyne R; Cancer Division, University College London Hospitals NHS Foundation Trust, London, UK.
  • Masento S; UCL Cancer Institute, London, UK.
  • Steventon L; Cancer Division, University College London Hospitals NHS Foundation Trust, London, UK.
  • Harmsworth King J; UCL Cancer Institute, London, UK.
  • Duncan N; Cancer Division, University College London Hospitals NHS Foundation Trust, London, UK.
  • Al Moubayed N; UCL Cancer Institute, London, UK.
Cancer Med ; 12(17): 17856-17865, 2023 09.
Article em En | MEDLINE | ID: mdl-37610318
ABSTRACT

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.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Bilirrubina / Aprendizado de Máquina Tipo de estudo: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Bilirrubina / Aprendizado de Máquina Tipo de estudo: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article