Abstract
Background
Many factors are implicated in the potential ‘under-treatment’ of prostate cancer but little is known about the between-hospital variation.
Methods
The National Prostate Cancer Audit (NPCA) database was used to identify high-risk localised or locally advanced prostate cancer patients in England, between January 2014 and December 2017, and the treatments received. Hospital-level variation in radical local treatment was explored visually using funnel plots. The intra-class correlation coefficient (ICC) quantified the between-hospital variation in a random-intercept multivariable logistic regression model.
Results
53,888 men, from 128 hospitals, were included and 35,034 (65.0%) received radical local treatment. The likelihood of receiving radical local treatment was increased in men who were younger (the strongest predictor), more affluent, those with fewer comorbidities, and in those with a non-Black ethnic background. There was more between-hospital variation (P < 0.001) for patients aged ≥80 years (ICC: 0.235) compared to patients aged 75–79 years (ICC: 0.070), 70–74 years (ICC: 0.041), and <70 years (ICC: 0.048). Comorbidity and socioeconomic deprivation did not influence the between-hospital variation.
Conclusions
Radical local treatment of high-risk localised or locally advanced prostate cancer depended strongly on age and comorbidity, but also on socioeconomic deprivation and ethnicity, with the between-hospital variation being highest in older patients.
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Data availability
The cancer registry data used for this study are based on information collected and quality assured by Public Health England’s National Cancer Registration Service (www.ncras.nhs.uk). Access to the data was facilitated by the Public Health England’s Office for Data Release. Hospital Episode Statistics were made available by the NHS Digital (www.digital.nhs.uk); all rights reserved. MGP had full access to all the data in the study and takes responsibility for the integrity of the data and accuracy of the data analysis. Data are not available to other researchers as it uses existing national data sets.
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Acknowledgements
We thank NHS staff for their support in collecting the clinical data, the National Cancer Registration and Analysis Service (www.ncras.nhs.uk) for providing cancer registry and radiotherapy data and NHS Digital (www.digital.nhs.uk) for providing Hospital Episode Statistics. MGP, JN, MM, TC, AS, BB, PC, NWC, HP, AA and JvdM are members of the Project Team of the National Prostate Cancer Audit (www.npca.org.uk). The National Prostate Cancer Audit is commissioned by the Healthcare Quality Improvement Partnership (www.hqip.org.uk) as part of the National Clinical Audit and Patient Outcomes Programme, and funded by NHS England and the Welsh Government. Neither HQIP nor NHS England or the Welsh Government had any involvement in the study design; in the collection, analysis, and interpretation of data; in the writing of the report; or in the decision to submit the article for publication. The researchers had full independence from the Healthcare Quality Improvement Partnership.
Funding
MGP was supported by a Doctoral Research Fellowship from the National Institute for Health Research (DRF-2018-11-ST2-036). BB was partly supported by an Academic Clinical Fellowship from the National Institute for Health Research. HP was supported by the University College London Hospitals/University College London Comprehensive Biomedical Research Centre. JvdM was partly supported by the National Institute for Health Research Collaboration for Leadership in Applied Health Research and Care North Thames. The views expressed in this article are solely those of the authors.
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Contributions
Designed the work: MGP, JvdM, HP and NWC. Analysed and interpreted data: MGP, JMB, JvdM, HP and NWC. Drafted article: MGP, JvdM, HP and NWC. Provided critical revision: All authors. Approved final version to be published: All authors.
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Competing interests
JvdM reports a contract with the Healthcare Quality Improvement Partnership for the provision of the National Prostate Cancer Audit (www.npca.org.uk) funded by the Healthcare Quality Improvement Partnership (www.hqip.org.uk). HP has attended and received honoraria for advisory boards, travel expenses to medical meetings, and served as a consultant for AstraZeneca, Astellas, Janssen, Sanofi Aventis, Takeda, Ipsen, Ferring, Sandoz, and Novartis. NWC has attended and received honoraria for advisory boards, travel expenses to medical meetings, and served as a consultant for AstraZeneca, Astellas, Bayer, Janssen, Sanofi Aventis, Takeda, Ipsen and Ferring.
Ethics approval and consent to participate
This study was exempt from NHS Research Ethics Committee approval because it involved analysis of pseudonymised linked data collated for the purpose of service evaluation as part of the National Prostate Cancer Audit.
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Parry, M.G., Boyle, J.M., Nossiter, J. et al. Determinants of variation in radical local treatment for men with high-risk localised or locally advanced prostate cancer in England. Prostate Cancer Prostatic Dis 26, 257–263 (2023). https://doi.org/10.1038/s41391-021-00439-9
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DOI: https://doi.org/10.1038/s41391-021-00439-9
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