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Validation of a bone scan positivity risk table in non-metastatic castration-resistant prostate cancer.

Authors :
Freedland SJ
Howard LE
Hanyok BT
Kadiyala VK
Kuang JY
Whitney CA
Wilks FR
Kane CJ
Terris MK
Amling CL
Cooperberg MR
Aronson WJ
Moreira DM
Source :
BJU international [BJU Int] 2016 Oct; Vol. 118 (4), pp. 570-7. Date of Electronic Publication: 2016 Feb 08.
Publication Year :
2016

Abstract

Objectives: To test the external validity of a previously developed risk table, designed to predict the probability of a positive bone scan among men with non-metastatic (M0) castration-resistant prostate cancer (CRPC), in a separate cohort.<br />Patients and Methods: We retrospectively analysed 429 bone scans of 281 patients with CRPC, with no known previous metastases, treated at three Veterans Affairs Medical Centers. We assessed the predictors of a positive scan using generalized estimating equations. Area under the curve (AUC), calibration plots and decision-curve analysis were used to assess the performance of our previous model to predict a positive scan in the current data.<br />Results: A total of 113 scans (26%) were positive. On multivariable analysis, the only significant predictors of a positive scan were log-transformed prostate-specific antigen (PSA): hazard ratio (HR) 2.13; 95% confidence interval (CI) 1.71-2.66 (P < 0.001) and log-transformed PSA doubling time (PSADT): HR 0.53; 95% CI 0.41-0.68 (P < 0.001). Among men with a PSA level <5 ng/mL, the rate of positive scans was 5%. The previously developed risk table had an AUC of 0.735 to predict positive bone scan with excellent calibration, and provided additional net benefit in the decision-curve analysis.<br />Conclusion: We have validated our previously developed table to predict the risk of a positive bone scan among men with M0/Mx CRPC. Use of this risk table may allow better tailoring of patients' scanning to identify metastases early, while minimizing over-imaging. Regardless of PSADT, positive bone scans were rare in men with a PSA <5 ng/mL.<br /> (© 2016 The Authors BJU International © 2016 BJU International Published by John Wiley & Sons Ltd.)

Details

Language :
English
ISSN :
1464-410X
Volume :
118
Issue :
4
Database :
MEDLINE
Journal :
BJU international
Publication Type :
Academic Journal
Accession number :
26762961
Full Text :
https://doi.org/10.1111/bju.13405