Real-world clinical outcomes among patients with localized prostate cancer (LPC) undergoing radical prostatectomy (RP).
Abstract
343 Background: RP is a curative option for LPC. While prognosis is generally favorable, patients with high-risk (HR) features face greater risk of recurrence and progression than those with low- or intermediate-risk (L/IR) disease. This study compared long-term outcomes of HR vs L/IR LPC patients treated with RP in the United States (US). Methods: This retrospective study used linked data from US community urology practices and administrative claims (PPS Analytics and Komodo Research Database; 1/1/2016–8/31/2024). The RP date served as the index date. Patients were stratified by HR vs L/IR status per NCCN guidelines based on TNM staging, Gleason score, and prostate-specific antigen level. Patients with metastasis, castration resistance, or advanced treatment before RP were excluded. Baseline characteristics (12 months pre-index) were balanced using inverse probability of treatment weighting. Outcomes including metastasis-free survival (time from index date to metastasis or death) and event-free survival (index date to biochemical recurrence, metastasis, or death) were compared via weighted Kaplan-Meier analyses and hazard ratios with 95% confidence intervals (CIs). Results: Overall, 18,971 patients with LPC were identified: 7,542 HR and 11,429 L/IR. After weighting, baseline characteristics were balanced between HR patients (mean age: 63.9 years, white: 52.6%, Medicare-insured: 46.8%, commercial-insured: 45.5%, median time from LPC diagnosis: 2.5 months, mean follow-up: 47.1 months) and L/IR patients (mean age: 63.6 years, white: 52.5%, Medicare-insured: 45.7%, commercial-insured: 46.7%, median time from LPC diagnosis: 2.8 months, mean follow-up 47.1 months). By 60 months, HR patients had a 3.59 greater rate of metastasis or death relative to L/IR patients (95% CI: 3.19, 4.04; p<0.001; Table). Rates of biochemical recurrence, metastasis, or death were also significantly higher in HR patients by 60 months (hazard ratio: 3.37; 95% CI: 3.18, 3.57; p<0.001). Conclusions: In this real-world analysis of patients with LPC treated with RP, those with HR disease had significantly worse metastasis-free and event-free survival than L/IR patients. These results highlight the greater clinical burden in HR LPC and the need for more effective treatment options. Clinical outcomes. Metastasis-free survival Event-free survival Kaplan-Meier rate High Risk Low/ Intermediate-risk High Risk Low/ Intermediate-risk 12 months 94.8% 98.9% 71.8% 92.0% HR (95% CI) 4.71 (3.86, 5.74); p<0.001 4.01 (3.71, 4.33); p<0.001 24 months 92.9% 98.2% 63.2% 88.1% HR (95% CI) 4.08 (3.46, 4.80); p<0.001 3.68 (3.45, 3.93); p<0.001 48 months 87.0% 96.4% 53.8% 82.9% HR (95% CI) 3.81 (3.35, 4.33); p<0.001 3.44 (3.24, 3.65); p<0.001 60 months 84.3% 95.1% 50.8% 80.7% HR (95% CI) 3.59 (3.19, 4.04); p<0.001 3.37 (3.18, 3.57); p<0.001 CI: confidence interval; HR: hazard ratio.
Article Details
Journal Info
Journal of Clinical Oncology
Lippincott Williams & Wilkins
Authors (12)
Neal D. Shore
START Carolinas/Carolina Urologic Research Center, Myrtle Beach, SC
Benjamin H. Lowentritt
Chesapeake Urology, Towson, MD
Charmi Patel
Johnson & Johnson, Horsham, PA
Frederic Kinkead
Analysis Group, Inc., Montréal, QC, Canada
Sabree Burbage
Johnson & Johnson, Horsham, PA
Carmine Rossi
3Analysis Group Inc, Montreal, Canada
Yuxi Wang
Gordon Wong
3University Health Network, Toronto, Canada
Francesca Lee
Analysis Group, Inc., Toronto, ON, Canada
Dominic Pilon
5Analysis Group, Inc., Montreal, Canada
Lawrence Ivan Karsh
AdventHealth Urology, Denver, CO
Gordon Andrew Brown
New Jersey Urology, A Summit Health Company, and Rowan University School of Osteopathic Medicine, Stratford, NJ