Abstract

BackgroundAspirin has been considered to be beneficial in preventing cardiovascular diseases and cancer. Several pharmaco-epidemiology cohort studies have shown protective effects of aspirin on diseases using various statistical methods, with the Cox regression model being the most commonly used approach. However, there are some inherent limitations to the conventional Cox regression approach such as guarantee-time bias, resulting in an overestimation of the drug effect. To overcome such limitations, alternative approaches, such as the time-dependent Cox model and landmark methods have been proposed. This study aimed to compare the performance of three methods: Cox regression, time-dependent Cox model and landmark method with different landmark times in order to address the problem of guarantee-time bias.MethodsThrough statistical modeling and simulation studies, the performance of the above three methods were assessed in terms of type I error, bias, power, and mean squared error (MSE). In addition, the three statistical approaches were applied to a real data example from the Korean National Health Insurance Database. Effect of cumulative rosiglitazone dose on the risk of hepatocellular carcinoma was used as an example for illustration.ResultsIn the simulated data, time-dependent Cox regression outperformed the landmark method in terms of bias and mean squared error but the type I error rates were similar. The results from real-data example showed the same patterns as the simulation findings.ConclusionsWhile both time-dependent Cox regression model and landmark analysis are useful in resolving the problem of guarantee-time bias, time-dependent Cox regression is the most appropriate method for analyzing cumulative dose effects in pharmaco-epidemiological studies.

Highlights

  • Aspirin has been considered to be beneficial in preventing cardiovascular diseases and cancer

  • For the purpose of this paper, we focus on guarantee-time bias, which is frequently encountered in time-to-event analyses evaluating drug effects

  • In the case of moderate and low-dose groups, the landmark method using landmark time 5 demonstrated higher statistical power compared to the time-dependent Cox regression

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Summary

Introduction

Aspirin has been considered to be beneficial in preventing cardiovascular diseases and cancer. Several pharmaco-epidemiology cohort studies have shown protective effects of aspirin on diseases using various statistical methods, with the Cox regression model being the most commonly used approach. There are some inherent limitations to the conventional Cox regression approach such as guarantee-time bias, resulting in an overestimation of the drug effect. To overcome such limitations, alternative approaches, such as the timedependent Cox model and landmark methods have been proposed. Findings of experimental studies have suggested that COX-2 suppression [7,8,9] or anti-platelet effect of aspirin [10, 11] could interact with cancer cells and play a significant role in blocking tumor angiogenesis, invasiveness and metastatic potential. Fraser et al [16] conducted a population-based study of breast cancer patients in Scotland, in which Cox’s proportional hazard models was used to

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