Abstract:
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In clinical studies, the outcome of interest is often a time-to-event. In addition, longitudinal biomarker data representing a partially-observed latent biological process may be collected. To capture the dependence between failure and the biomarker process, a joint model is needed. In this joint model, the cumulative hazard of failure can be modeled as a Lévy process with a continuous time transformation representing the accumulated risk of failure. We derive the survival and hazard functions of failure under the assumption of a Gamma process cumulative hazard and different observation mechanisms for the biomarker. We focus on the case of marked survival wherein the marker and event are observed simultaneously. We apply our method to SEER prostate cancer incidence data, where men diagnosed with prostate cancer have prostate specific antigen (PSA) collected at diagnosis.
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