Competing risks analysis with missing cause-of-failure—penalized likelihood estimation of cause-specific Cox models

Author:

Lô Serigne N123ORCID,Ma Jun4,Manuguerra Maurizio4ORCID,Moreno-Betancur Margarita56ORCID,Scolyer Richard A1278ORCID,Thompson John F129

Affiliation:

1. Melanoma Institute Australia, The University of Sydney, Sydney, NSW, Australia

2. Faculty of Medicine and Health, The University of Sydney, Sydney, NSW, Australia

3. Institute for Research and Medical Consultations (IRMC), Imam Abdulrahman Bin Faisal University, Dammam, Saudi Arabia

4. Department of Mathematics and Statistics, Macquarie University, NSW, Australia

5. Clinical Epidemiology and Biostatistics Unit, Department of Paediatrics, University of Melbourne, VIC, Australia

6. Clinical Epidemiology and Biostatistics Unit, Murdoch Children’s Research Institute, VIC, Australia

7. Tissue Pathology and Diagnostic Oncology, Royal Prince Alfred Hospital and NSW Health Pathology, Sydney, NSW, Australia

8. Charles Perkins Centre, The University of Sydney, NSW, Sydney, Australia

9. Department of Melanoma and Surgical Oncology, Royal Prince Alfred Hospital, Sydney, NSW, Australia

Abstract

Competing risks models are attractive tools to analyze time-to-event data where several causes of an event are competing. However, a complexity may arise when, for instance, some subjects experience the event of interest but the causes are not known. Assuming that unknown causes of events are missing at random, we developed a novel constrained maximum penalized likelihood method for fitting semi-parametric cause-specific Cox regression models. Here, penalty functions were used to smooth the baseline hazards. An appealing feature of this approach is that all the relevant estimands in competing risks models are estimated including cause-specific hazard ratios, cause-specific baseline hazards, and cumulative incidence functions. Asymptotic results for these estimators were also developed, allowing for direct inferences. The proposed method was compared with some existing methods through a simulation study. A real data example was analyzed using the new method to evaluate the association of age at diagnosis with melanoma-death and non-melanoma-death in patients diagnosed with thin melanoma (tumour thickness [Formula: see text]1.0  mm). An R function for our proposed method is currently available on GitHub and will be included in the R package "survivalMPL" at CRAN.

Publisher

SAGE Publications

Subject

Health Information Management,Statistics and Probability,Epidemiology

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