Estimation of Relative and Absolute Risks in a Competing-Risks Setting Using a Nested Case-Control Study Design: Example From the ProMort Study

Author:

Zelic Renata1,Zugna Daniela23,Bottai Matteo4,Andrén Ove5,Fridfeldt Jonna5,Carlsson Jessica5,Davidsson Sabina5,Fiano Valentina23,Fiorentino Michelangelo6,Giunchi Francesca6,Grasso Chiara23,Lianas Luca7,Mascia Cecilia7,Molinaro Luca8,Zanetti Gianluigi7ORCID,Richiardi Lorenzo23,Pettersson Andreas1,Akre Olof910

Affiliation:

1. Clinical Epidemiology Unit, Department of Medicine Solna, Karolinska Institutet, Stockholm, Sweden

2. Cancer Epidemiology Unit, Department of Medical Sciences, University of Turin, Turin, Italy

3. Centro di Riferimento per l’Epidemiologia e la Prevenzione Oncologica

4. Unit of Biostatistics, Institute of Environmental Medicine, Karolinska Institutet, Stockholm, Sweden

5. Department of Urology, Faculty of Medicine and Health, Örebro University, Örebro, Sweden

6. Pathology Service, Addarii Institute of Oncology, Sant’Orsola-Malpighi Hospital, Bologna, Italy

7. Data-Intensive Computing Division, Center for Advanced Studies, Research and Development in Sardinia, Pula, Italy

8. Division of Pathology, Azienda Ospedaliero-Universitaria Città della Salute e della Scienza Hospital, Turin, Italy

9. Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden

10. Department of Urology, Karolinska University Hospital, Stockholm, Sweden

Abstract

Abstract In this paper, we describe the Prognostic Factors for Mortality in Prostate Cancer (ProMort) study and use it to demonstrate how the weighted likelihood method can be used in nested case-control studies to estimate both relative and absolute risks in the competing-risks setting. ProMort is a case-control study nested within the National Prostate Cancer Register (NPCR) of Sweden, comprising 1,710 men diagnosed with low- or intermediate-risk prostate cancer between 1998 and 2011 who died from prostate cancer (cases) and 1,710 matched controls. Cause-specific hazard ratios and cumulative incidence functions (CIFs) for prostate cancer death were estimated in ProMort using weighted flexible parametric models and compared with the corresponding estimates from the NPCR cohort. We further drew 1,500 random nested case-control subsamples of the NPCR cohort and quantified the bias in the hazard ratio and CIF estimates. Finally, we compared the ProMort estimates with those obtained by augmenting competing-risks cases and by augmenting both competing-risks cases and controls. The hazard ratios for prostate cancer death estimated in ProMort were comparable to those in the NPCR. The hazard ratios for dying from other causes were biased, which introduced bias in the CIFs estimated in the competing-risks setting. When augmenting both competing-risks cases and controls, the bias was reduced.

Funder

Karolinska Institutet

Swedish Cancer Society

Italian Association for Cancer Research

Sardinian Regional Authorities

Publisher

Oxford University Press (OUP)

Subject

Epidemiology

Reference37 articles.

1. Contemporary trends in low risk prostate cancer: risk assessment and treatment;Cooperberg;J Urol,2007

2. Long-term outcomes among noncuratively treated men according to prostate cancer risk category in a nationwide, population-based study;Rider;Eur Urol,2013

3. Prostate cancer: summary of updated NICE guidance;Graham;BMJ,2014

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