Abstract
Background: Progression-free survival (PFS) is used to evaluate treatment effects in cancer clinical trials. Disease progression (DP) in patients is typically determined by radiological testing at several scheduled tumor-assessment time points. This produces a discrepancy between the true progression time and the observed progression time. When the observed progression time is considered as the true progression time, a positively biased PFS is obtained for some patients, and the estimated survival function derived by the Kaplan–Meier method is also biased. Methods: While the midpoint imputation method is available and replaces interval-censored data with midpoint data, it unrealistically assumes that several DPs occur at the same time point when several DPs are observed within the same tumor-assessment interval. We enhanced the midpoint imputation method by replacing interval-censored data with equally spaced timepoint data based on the number of observed interval-censored data within the same tumor-assessment interval. Results: The root mean square error of the median of the enhanced method is almost always smaller than that of the midpoint imputation regardless of the tumor-assessment frequency. The coverage probability of the enhanced method is close to the nominal confidence level of 95% in most scenarios. Conclusion: We believe that the enhanced method, which builds upon the midpoint imputation method, is more effective than the midpoint imputation method itself.
| Original language | English |
|---|---|
| Pages (from-to) | 721-729 |
| Number of pages | 9 |
| Journal | Therapeutic Innovation and Regulatory Science |
| Volume | 58 |
| Issue number | 4 |
| DOIs | |
| Publication status | Published - Jul 2024 |
Keywords
- Cancer clinical trial
- Interval censoring
- Median survival time
- Progression-free survival
- Survival analysis
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