TY - JOUR
T1 - Active surveillance in younger men with prostate cancer
AU - Leapman, Michael S.
AU - Cowan, Janet E.
AU - Nguyen, Hao G.
AU - Shinohara, Katsuto K.
AU - Perez, Nannette
AU - Cooperberg, Matthew R.
AU - Catalona, William J.
AU - Carroll, Peter R.
N1 - Funding Information:
Supported by US Department of Defense Transformative Impact Aware Prostate Cancer Research Program Grant No. W81XWH-13-2-0074 (M.R.C., P.R.C.); National Cancer Institute Grants No. P50 CA1809952, U01CA089600-10A1, and P30CA60553; and the Urological Research Foundation (W.J.C.).
Publisher Copyright:
© 2017 by American Society of Clinical Oncology.
PY - 2017/6/10
Y1 - 2017/6/10
N2 - Purpose: The suitability of younger patients with prostate cancer (PCa) for initial active surveillance (AS) has been questioned on the basis of eventual treatment necessity and concerns of safety; however, the role of age on surveillance outcomes has not been well defined. Patients and Methods: We identified men managed with AS at our institution with a minimum follow-up of 6 months. The primary study objective was to examine the association of age with risk of biopsy-based Gleason score upgrade during AS. We also examined the association of age with related end points, including overall biopsy-determined progression, definitive treatment, and pathologic and biochemical outcomes after delayed radical prostatectomy (RP), using descriptive statistics, the Kaplan-Meier method, and multivariable Cox proportional hazards regression. Results: A total of 1,433 patients were followed for a median of 49 months; 74% underwent initial biopsy at a referring institution. Median age at diagnosis was 63 years, including 599 patients (42%) # 60 years old and 834 (58%) . 60 years old. The 3- and 5-year biopsy-based Gleason score upgrade-free rates were 73% and 55%, respectively, for men # 60 years old compared with 64% and 48%, respectively, for men older than 60 years (P, .01). On Cox regression analysis, younger age was independently associated with lower risk of biopsy-based Gleason score upgrade (hazard ratio per 1-year decrease, 0.969 [95% CI, 0.956 to 0.983]; P, .01), and persisted upon restriction to men meeting strict AS inclusion criteria. There was no significant association between younger age and risk of definitive treatment or risk of biochemical recurrence after delayed RP. Conclusion: Younger patient age was associated with decreased risk of biopsy-based Gleason score upgrade during AS but not with risk of definitive treatment in the intermediate term. AS represents a strategy to mitigate overtreatment in young patients with low-risk PCa in the early term.
AB - Purpose: The suitability of younger patients with prostate cancer (PCa) for initial active surveillance (AS) has been questioned on the basis of eventual treatment necessity and concerns of safety; however, the role of age on surveillance outcomes has not been well defined. Patients and Methods: We identified men managed with AS at our institution with a minimum follow-up of 6 months. The primary study objective was to examine the association of age with risk of biopsy-based Gleason score upgrade during AS. We also examined the association of age with related end points, including overall biopsy-determined progression, definitive treatment, and pathologic and biochemical outcomes after delayed radical prostatectomy (RP), using descriptive statistics, the Kaplan-Meier method, and multivariable Cox proportional hazards regression. Results: A total of 1,433 patients were followed for a median of 49 months; 74% underwent initial biopsy at a referring institution. Median age at diagnosis was 63 years, including 599 patients (42%) # 60 years old and 834 (58%) . 60 years old. The 3- and 5-year biopsy-based Gleason score upgrade-free rates were 73% and 55%, respectively, for men # 60 years old compared with 64% and 48%, respectively, for men older than 60 years (P, .01). On Cox regression analysis, younger age was independently associated with lower risk of biopsy-based Gleason score upgrade (hazard ratio per 1-year decrease, 0.969 [95% CI, 0.956 to 0.983]; P, .01), and persisted upon restriction to men meeting strict AS inclusion criteria. There was no significant association between younger age and risk of definitive treatment or risk of biochemical recurrence after delayed RP. Conclusion: Younger patient age was associated with decreased risk of biopsy-based Gleason score upgrade during AS but not with risk of definitive treatment in the intermediate term. AS represents a strategy to mitigate overtreatment in young patients with low-risk PCa in the early term.
UR - http://www.scopus.com/inward/record.url?scp=85021740359&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85021740359&partnerID=8YFLogxK
U2 - 10.1200/JCO.2016.68.0058
DO - 10.1200/JCO.2016.68.0058
M3 - Article
C2 - 28346806
AN - SCOPUS:85021740359
SN - 0732-183X
VL - 35
SP - 1898
EP - 1904
JO - Journal of Clinical Oncology
JF - Journal of Clinical Oncology
IS - 17
ER -