Abstract

BackgroundTo determine how much an augmented analysis approach could improve the efficiency of prostate-specific antigen (PSA) response analyses in clinical practice. PSA response rates are commonly used outcome measures in metastatic castration-resistant prostate cancer (mCRPC) trial reports. PSA response is evaluated by comparing continuous PSA data (e.g., change from baseline) to a threshold (e.g., 50% reduction). Consequently, information in the continuous data is discarded. Recent papers have proposed an augmented approach that retains the conventional response rate, but employs the continuous data to improve precision of estimation.MethodsA literature review identified published prostate cancer trials that included a waterfall plot of continuous PSA data. This continuous data was extracted to enable the conventional and augmented approaches to be compared.ResultsSixty-four articles, reporting results for 78 mCRPC treatment arms, were re-analysed. The median efficiency gain from using the augmented analysis, in terms of the implied increase to the sample size of the original study, was 103.2% (IQR [89.8,190.9%]).ConclusionsAugmented PSA response analysis requires no additional data to be collected and can be performed easily using available software. It improves precision of estimation to a degree that is equivalent to a substantial sample size increase. The implication of this work is that prostate cancer trials using PSA response as a primary endpoint could be delivered with fewer participants and, therefore, more rapidly with reduced cost.

Highlights

  • To determine how much an augmented analysis approach could improve the efficiency of prostatespecific antigen (PSA) response analyses in clinical practice

  • Given the important role PSA response rates have in metastatic castration-resistant prostate cancer (mCRPC) settings, we planned to focus our analyses on trials in this domain

  • Included articles Ninety-eight articles reporting results for 121 treatment arms were identified for which re-analysis could be performed, including 64 articles reporting 78 mCRPC treatment arms (Fig. 1)

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Summary

Introduction

To determine how much an augmented analysis approach could improve the efficiency of prostatespecific antigen (PSA) response analyses in clinical practice. PSA response is evaluated by comparing continuous PSA data (e.g., change from baseline) to a threshold (e.g., 50% reduction). Recent papers have proposed an augmented approach that retains the conventional response rate, but employs the continuous data to improve precision of estimation. The first Prostate Cancer Clinical Trials Working Group (PCWG1) recommended defining PSA response as a ≥ 50% decrease from baseline [7]. This was updated in the PCWG2 guidance [8] to suggest avoiding reporting PSA response rates and instead provide waterfall plots of PSA change. PCWG2 recommended PSA progression as an endpoint, defined as a 25% increase in PSA. These recommendations were retained in the PCWG3 guidance [9]

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