Abstract

Predictive and prognostic models hold great potential to support clinical decision making in oncology and could ultimately facilitate a paradigm shift to a more personalised form of treatment. While a large number of models relevant to the field of oncology have been developed, few have been translated into clinical use and assessment of clinical utility is not currently considered a routine part of model development. In this narrative review of the clinical evaluation of prediction models in oncology, we propose a high-level process diagram for the life cycle of a clinical model, encompassing model commissioning, clinical implementation and ongoing quality assurance, which aims to bridge the gap between model development and clinical implementation.

Highlights

  • Oncology ranks among the most complex disciplines of modern medicine

  • Predictive and prognostic models hold great potential to support clinical decision making in oncology and could facilitate a paradigm shift to a more personalised form of treatment

  • A major advantage of these models is that they can be developed using real-world data generated by patients treated in routine clinical practice, thereby providing a new form of evidence that is more inclusive of the patient groups commonly under-represented in traditional clinical trials

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Summary

Introduction

Oncology ranks among the most complex disciplines of modern medicine. The inherent heterogeneity of cancer, patients and the ever-expanding number of treatment options make the selection of optimal treatment regimens more challenging than ever. The Predict breast tool is an example of a CPM enriched by causal reasoning, as it uses population average outcomes from clinical trials to provide survival estimates for different treatment combinations [6]. Reported advantages from the clinician perspective include supplementing their existing clinical knowledge, with the more accurate prediction they provide enhancing decision making confidence and potentially improving patient outcomes [22e25].

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Conclusion

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