Skip to search boxSkip to navigationSkip to main content

Predictors of Time to Metastasis in Castration-resistant Prostate Cancer

  • Daniel M. Moreira(corresponding author)
    ,
  • Lauren E. Howard
    ,
  • Katharine N. Sourbeer
    ,
  • Hiruni S. Amarasekara
    ,
  • Lydia C. Chow
    ,
  • Dillon C. Cockrell
*Corresponding author for this work
  • Mayo Clinic Rochester, MN
    ,
  • Duke University
    ,
  • Durham Veterans Affairs Medical Center
    ,
  • VA Medical Center
    ,
  • University of California at Los Angeles
    ,
  • University of California at San Diego
Scholary Output:
Contribution to journal
Article
Peer-review

Open access

Sustainable Development Goals

  • SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well

Abstract

Objective To investigate predictors of time to metastasis among men treated with androgen deprivation therapy for nonmetastatic prostate cancer who developed castration-resistant prostate cancer (CRPC) within the Shared Equal Access Regional Cancer Hospital cohort. Methods This is a retrospective analysis of 458 nonmetastatic CRPC men. Metastases were detected in routine bone scans or other imaging tests. Predictors of time to metastasis were analyzed using proportional hazards model with CRPC as time zero. Results A total of 256 (56%) men were diagnosed with metastatic disease over a median follow-up of 36 months. Metastasis-free survival was 79%, 65%, 52%, 47%, and 41% at 1, 2, 3, 4, and 5 years after CRPC, respectively. In multivariable analysis, Gleason score 8-10 (hazard ratio [HR] = 1.61; P = .026), receiving primary localized treatment (HR = 1.38; P = .028), higher prostate-specific antigen (PSA) levels at CRPC diagnosis (logPSA HR = 1.64; P < .001), and PSA doubling time ≤6 months (HR = 1.42; P = .040) were independently associated with shorter time to metastasis. Race, year of CRPC, age, and time from androgen deprivation therapy to CRPC were not associated with metastasis. Conclusion Among nonmetastatic CRPC men, nearly 60% developed metastatic disease during the first 5 years, with most of the metastasis occurring within the first 3 years. Higher Gleason score, receiving primary treatment, higher PSA, and shorter PSA doubling time were independently associated with shorter time to metastasis. Therefore, these variables can be used to stratify patients according to metastasis risk.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 171-176 (6 pages)

Journal (Volume, Issue Number)

Urology (Volume 96)

Publication milestones

  • Accepted/In press - 02/01/2016
  • Published - 10/01/2016

Publication status

Published - 10/01/2016

ISSN

0090-4295

Publication IDs

  • Scopus: 84979700763
  • PubMed: 27318265

Publication metrics

Metrics

Fractional count
1
Fractional count
0.07
Fractional count
13
Fractional count
0.93
Fractional count
1
Fractional count
1
Scopus
citations
SciVal
FWCI
1.79
SciVal
Author count
14
SciVal
citations
25
SciVal
Paper percentile
89

PlumX, opens in new tab

Captures
67
Citation count
61

Funding Details

Funding Support: Department of Veterans Affairs, National Institute of Health R01CA100938 (WJA), NIH Specialized Programs of Research Excellence Grant P50 CA92131-01A1 (WJA), the Georgia Cancer Coalition (MKT), NIH K24 CA160653 (SJF), NIH/NCI P50CA09231 (WJA), and Amgen .
FundersFunding numbers
MKT
K24 CA160653
NIH
P50 CA92131-01A1
NCI
R01CA100938, K24CA160653, P50CA09231
VA
-
GCC
-
Amgen
-