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PSA Doubling Time and Absolute PSA Predict Metastasis-free Survival in Men With Biochemically Recurrent Prostate Cancer After Radical Prostatectomy

  • Mark C. Markowski
  • , Yongmei Chen
  • , Zhaoyong Feng
  • , Jennifer Cullen
  • , Bruce J. Trock
  • , Daniel Suzman
  • , Emmanuel S. Antonarakis
  • , Channing J. Paller
  • , Inger Rosner
  • , Misop Han
  • , Patrick C. Walsh
  • , Alan W. Partin
  • , Mario Eisenberger

Research output: Contribution to journalArticlepeer-review

Abstract

Introduction: The aim of this study was to investigate the association of prostate-specific antigen (PSA) values on metastasis-free survival (MFS) in men with biochemically recurrent prostate cancer (BRPC) and PSA doubling time (PSADT) < 12 months. This dataset also reflects an update with longer follow-up of our prior publications on the natural history of BRPC in the absence of treatment. Materials and Methods: In this report, we combined databases from the Center for Prostate Disease Research and Johns Hopkins University (CPDR/JHU). In the CPDR/JHU radical prostatectomy database (30,936 total patients), 656 men with BRPC (> 0.2 ng/mL) after prostatectomy and PSADT < 12 months, who received no adjuvant/salvage androgen deprivation and/or radiation therapy, were prospectively followed until radiologic evidence of metastasis and are included in this analysis. Results: Metastasis occurred in 250 of 656 patients with BRPC (median follow-up, 5 years). PSADT < 7.5 months and Gleason score were independent risk factors for distant metastasis in multivariable analysis. Risk of metastasis increased for PSADT 6.01 to 7.50, 4.51 to 6.0, 3.01 to 4.50, and ≤ 3.0 months, after adjusting for Gleason score. A PSA value ≥ 0.5 ng/mL significantly and independently increased risk of metastasis in patients with PSADT < 12 months (hazard ratio, 2.79; 95% confidence interval, 1.47-5.29; P = .001). Conclusions: In men with PSADT < 12 months, PSADT ≤ 7.5 months, PSA ≥ 0.5 ng/mL, and Gleason score are independent predictors of MFS on multivariable analysis.

Original languageEnglish (US)
Pages (from-to)470-475.e1
JournalClinical Genitourinary Cancer
Volume17
Issue number6
DOIs
StatePublished - Dec 2019
Externally publishedYes

Bibliographical note

Funding Information:
The project described was supported by the Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins with National Institutes of Health grants P30 CA006973 and a PCF Young Investigator Award. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Cancer Institute or the National Institutes of Health.

Funding Information:
The project described was supported by the Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins with National Institutes of Health grants P30 CA006973 and a PCF Young Investigator Award. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Cancer Institute or the National Institutes of Health.

Publisher Copyright:
© 2019 Elsevier Inc.

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Biochemical recurrence
  • Deferred ADT
  • Natural history
  • PSA cut-point
  • Post-prostatectomy

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