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      Assessing accuracy of Weibull shape parameter estimate from historical studies for subsequent sample size calculation in clinical trials with time-to-event outcome

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          Abstract

          Background

          Recent developments in literature on sample size calculations for time-to-event outcomes involve assumption of Weibull distributed times. These methods require a point estimate of the Weibull shape parameter obtained from historical studies. However, very limited guidance exists in published literature to assess how reliable this point estimate is when it is obtained from published results of a historical study.

          Methods

          We conduct simulations to assess how accurate and reliable the point estimate of the Weibull shape parameter is when it is estimated from published results of median survival time and/or corresponding interquartile range. Accuracy of this estimate is assessed using the criteria of average relative bias, root mean square error, and coefficient of variation for various combinations of sample sizes and censoring rates. Sensitivity of these calculations is assessed first, by increasing the number of survival quantiles used to calculate accuracy, and second, by using the full Kaplan Meier (KM) curve from the historical study.

          Results

          Our simulations suggest that point estimate of the shape parameter is reasonably accurate when estimated from historical studies with sample size ≥ 50 with censoring rate approximately 20%. Knowledge of the median and inter-quartile range seems to be adequate for this purpose. For historical studies with small sample sizes or higher censoring rates, more information needs to be abstracted from the published KM curves to improve accuracy.

          Conclusions

          We conclude that assessing the accuracy of Weibull shape parameter estimate is important before it can be used to conduct sample size calculations for a subsequent trial.

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          Most cited references15

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          Comparing survival of a sample to that of a standard population.

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            Second-line systemic treatment for advanced cholangiocarcinoma.

            Gemcitabine plus platinum (GEM-P) combination chemotherapy is standard treatment for first-line advanced cholangiocarcinoma (aCC). GEM-P first-line therapy reports a progression-free survival (PFS) of 8 months and overall survival (OS) of 11.7 months. Treatment in the second-line setting is less clear. Five-year survival for aCC remains dismal at 5-10%. The purpose of this study was to describe the outcomes with second-line systemic treatment at our institution.
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              Sample size calculation for the one-sample log-rank test

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                Author and article information

                Contributors
                Journal
                Contemp Clin Trials Commun
                Contemp Clin Trials Commun
                Contemporary Clinical Trials Communications
                Elsevier
                2451-8654
                26 February 2020
                March 2020
                26 February 2020
                : 17
                : 100548
                Affiliations
                [1]Department of Biostatistics and Data Science, University of Kansas Medical Center, Kansas City, KS, USA
                Author notes
                []Corresponding author. 3901 Rainbow Boulevard, Kansas City, KS, 66160, USA. mphadnis@ 123456kumc.edu
                Article
                S2451-8654(20)30032-6 100548
                10.1016/j.conctc.2020.100548
                7052506
                69001bb0-0172-4b50-a305-863f8f207045
                © 2020 The Authors

                This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).

                History
                : 8 August 2019
                : 14 February 2020
                : 22 February 2020
                Categories
                Article

                censoring,historical data,km curves,sample size,shape parameter,weibull

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