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Kathryn C. Fitzgerald

Harvard TH Chan School of Public Health



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Robert J. Glynn

Harvard TH Chan School of Public Health



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Rulla M. Tamimi

Harvard TH Chan School of Public Health



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Wendy Y. Chen

Brigham and Women's Hospital and Harvard Medical School



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Graham C. Colditz

Harvard TH Chan School of Public Health



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Susan Hankinson

Harvard TH Chan School of Public Health



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Bernard Rosner

Brigham and Women's Hospital and Harvard Medical School



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194 – Contributed Oral Poster Presentations: ENAR

Risk Factors and Outcomes in a Multiple Tumor Marker Setting: The Issues of Correlated and Missing Tumor Markers

Sponsor: ENAR
Keywords: Breast cancer, competing risks, proportional hazards model, missing data, multiple imputation, inverse probability weighting

Kathryn C. Fitzgerald

Harvard TH Chan School of Public Health

Robert J. Glynn

Harvard TH Chan School of Public Health

Rulla M. Tamimi

Harvard TH Chan School of Public Health

Wendy Y. Chen

Brigham and Women's Hospital and Harvard Medical School

Graham C. Colditz

Harvard TH Chan School of Public Health

Susan Hankinson

Harvard TH Chan School of Public Health

Bernard Rosner

Brigham and Women's Hospital and Harvard Medical School

Risk profiles for cancer outcomes often vary by the presence of different tumor markers or subtypes. Increasing the number of markers adds an additional layer of complexity as markers are often correlated, and as a result, leads to difficulty in assessing subtype-specific effects of particular risk factors without considering other markers. Scientifically, it's also of interest to identify which marker or combination of markers is most relevant for disease. Finally, with a larger number of markers, the likelihood of missing marker information also increases and raises the question as to how to properly address this issue. In this paper, we apply methodology originally introduced by Rosner et al. to compute adjusted hazard-ratios that account for multiple correlated markers while evaluating four candidate approaches for missing tumor subtype. We consider the complete case, missing indicator, inverse probability weighting and multiple imputation approaches for missing tumor markers. We evaluate these four approaches using simulation studies and apply each to a real study of breast cancer risk factors considering multiple subtypes.

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