Skip to search boxSkip to navigationSkip to main content

Extraprostatic Extension in Core Biopsies Epitomizes High-risk but Locally Treatable Prostate Cancer

  • Hanan Goldberg(corresponding author)
    ,
  • Abu Hijlih Ramiz
    ,
  • Rachel Glicksman
    ,
  • Noelia S. Salgado
    ,
  • Thenappan Chandrasekar
    ,
*Corresponding author for this work
Scholary Output:
Contribution to journal
Article
Peer-review

Sustainable Development Goals

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

Abstract

Background: Extraprostatic extension (EPE) is defined as local spread of prostate cancer (PC) beyond prostate boundaries. Although extensively evaluated in radical prostatectomy (RP) specimens, its significance in prostate biopsy (PB) specimens is understudied. Objective: To analyze the clinicopathologic characteristics and treatment outcomes for patients with nonmetastatic PC with EPE on diagnostic PB. Design, setting, and participants: We identified all patients at Princess Margaret Cancer Center with EPE on their diagnostic PB between 2005 and 2016. All patients underwent definitive curative-intent treatment with either RP or radiotherapy (RT) with or without androgen deprivation therapy (ADT). Outcome measurements and statistical analyses: Clinicopathologic variables were compared using a χ2 or Kruskal-Wallis test; log-rank analyses were applied for outcomes comparison. Primary and secondary endpoints were 5-yr biochemical recurrence (BCR) and the occurrence of metastasis or cancer-specific death, respectively. Results and limitations: A total of 127 patients with reported EPE in their PB were identified. One-third of patients underwent RP (n = 43) and two-thirds received RT (n = 84). Baseline prognostic variables (prostate-specific antigen, clinical T stage, biopsy pathologic grade group, and proportion of cores involved with PC) were similar between the treatment groups. More than two-thirds of RT patients received concomitant ADT (median duration 36 mo, interquartile range 24–36), while 39.5% of RP patients received postoperative radiotherapy ± ADT. Of the RP patients, 95.3% had ≥pT3a disease and 27.9% had pN1 disease. Median follow-up after RP and RT was similar (43.7 vs 45.8 mo; p = 0.516). The 5-yr BCR and metastasis rates in the RP versus RT groups were 25.6% versus 11.9% (p = 0.09) and 7% versus 11.9% (p = 0.386), respectively. Only one patient died from metastatic PC (RT group). Limitations include the single-center and retrospective design with a moderate sample size and relatively short follow-up. Conclusions: EPE on PB is an infrequent finding that is strongly associated with high-risk clinicopathologic prognostic features that accurately predict EPE in RP specimens. Despite entailing aggressive disease characteristics, EPE on PB should not preclude patients from receiving definitive radical local therapy. Patient summary: Extraprostatic extension on prostate biopsies is an uncommon finding, but is strongly correlated to additional aggressive disease features. This finding accurately predicts the presence of extraprostatic extension on the final prostate specimen after surgery. Despite the associated high-risk features, finding extraprostatic extension in prostate biopsies should not preclude patients from undergoing curative-intent radical local therapy. Extraprostatic extension (EPE) on prostate biopsy is correlated with high-risk prostate cancer features, and predicts EPE on the final specimen. Despite its association with high = risk features, this finding should not preclude patients from receiving definitive local treatment.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 88-96 (9 pages)

Journal (Volume, Issue Number)

European Urology Oncology (Volume 2, Issue 1)

Publication milestones

  • Published - 02/2019

Publication status

Published - 02/2019

Publication IDs

  • Scopus: 85062800766
  • PubMed: 30929849

Publication metrics

Metrics

Fractional count
1
Fractional count
0.05
Fractional count
19
Fractional count
0.95
Fractional count
1
Fractional count
1
Scopus
citations
SciVal
FWCI
0.22
SciVal
Author count
20
SciVal
citations
1
SciVal
Paper percentile
49

PlumX, opens in new tab

Captures
31
Citation count
6