Overall survival in metastatic castration-resistant prostate cancer (mCRPC): A retrospective electronic medical record analysis of men treated with sipuleucel-T in community urology over 14 years.

e17041 Background: Treating mCRPC remains challenging, with limited options for prolonging overall survival (OS). Sipuleucel-T, an autologous prostate-specific antigen (PSA)-targeting cellular immunotherapy (therapeutic vaccine), was FDA-approved in April 2010. We examined the outcomes of treatment for mCRPC since 2010 in SoNaR for Prostate Cancer, the deidentified PPS Analytics/Specialty Networks Uro-oncology electronic medical record (EMR) database that encompasses 90 United States (US) community urology practices with over 3,200 providers. Methods: This multicenter, retrospective study analyzed OS in 2 cohorts of men aged ≥18 years who were diagnosed with mCRPC between January 1, 2010 and May 31, 2024 and treated (Cohort 1) or not treated (Cohort 2) with sipuleucel-T in community urology settings. For the preliminary covariates of race, US region, and age and Gleason group scores at diagnosis, patient characteristics were summarized descriptively, Kaplan-Meier (KM) methods and log-rank tests compared OS, and Cox proportional hazards estimated hazard ratios (HRs). Results: Of a total 11,265 men, 46.9% received sipuleucel-T (Cohort 1). Data from the the sipuleucel-T-treated cohort are described in text; all patients are described in the table. Mean age was 73.4 years, 14% were Black, and 46% were in the Southern US region (Table). At PC diagnosis, the mean Gleason score was 7.3, categorizing 53% as high-risk. At mCRPC diagnosis, the mean PSA level was 49.1 ng/mL (median 6.3 ng/mL). Median OS was 44 months (Table). Among the 4,494 patients of cohort 1 with known status, 28% were still alive 5 years after treatment; their median OS was 97 months. Conclusions: Despite their high-risk disease, patients who received sipuleucel-T had a 44-month median OS, with 28% being alive at 5 years later. This highlights the potential therapeutic benefit of integrating sipuleucel-T into real-world treatment for mCRPC. Further analysis is needed, leveraging the rich nature of this dataset. Supported by Dendreon Pharmaceuticals, LLC. Patient characteristics and outcomes. Overall (n=11,265) Cohort 1Sipuleucel-T (n=5,281) Cohort 2No Sipuleucel-T(n=5,984) P -value, Cohort 1 vs 2 Median age, years 76 74 78 <0.001 Race, % (White/Black/Other) 67/15/19 69/14/17 65/15/21 <0.001 US region, % (Midwest/Northeast/South/West) 25/16/45/14 25/16/46/13 26/16/44/14 0.124 PSA at mCRPC diagnosis (mean/median) 81.1/8.0 49.1/6.3 110.0/10.3 <0.001 Gleason score at PC diagnosis, mean 7.3 7.3 7.2 0.064 Alive at 5 years, % 20% 28% 12% <0.001 KM OS (median, 95% CI), months 33 (32, 34) 44 (43, 46) 24 (24, 25) HR (95%CI), Cohort 1 vs 2 1.7 (1.6-1.8)<0.001 CI, confidence interval.

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Publication Details

Journal
Journal of Clinical Oncology
Published
2025-05-28
DOI
https://doi.org/10.1200/jco.2025.43.16_suppl.e17041
Primary Topic
Prostate Cancer Treatment and Research
Type
article
Field-Weighted Citation Impact
0.00

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article

Overall survival in metastatic castration-resistant prostate cancer (mCRPC): A retrospective electronic medical record analysis of men treated with sipuleucel-T in community urology over 14 years.

Jason Hafron, Bryan A. Mehlhaff, Nicholas Lazarou, Paul Sieber et al.
Journal of Clinical Oncology
Prostate Cancer Treatment and Research
article

Overall survival in metastatic castration-resistant prostate cancer (mCRPC): A retrospective electronic medical record analysis of men treated with sipuleucel-T in community urology over 14 years.

Jason Hafron, Bryan A. Mehlhaff, Nicholas Lazarou, Paul Sieber, Lawrence I. Karsh, Benjamin Lowentritt, Katie Grant, Paul Monk, Nadeem A. Sheikh, Lorraine O'Donnell, Bart J. Wilson, Matthew Harmon, Christopher Michael Pieczonka, Neal D. Shore, Michael D. Fabrizio, Arpit Kashyap, Margaret Warner-Lubin
article en

Abstract

e17041 Background: Treating mCRPC remains challenging, with limited options for prolonging overall survival (OS). Sipuleucel-T, an autologous prostate-specific antigen (PSA)-targeting cellular immunotherapy (therapeutic vaccine), was FDA-approved in April 2010. We examined the outcomes of treatment for mCRPC since 2010 in SoNaR for Prostate Cancer, the deidentified PPS Analytics/Specialty Networks Uro-oncology electronic medical record (EMR) database that encompasses 90 United States (US) community urology practices with over 3,200 providers. Methods: This multicenter, retrospective study analyzed OS in 2 cohorts of men aged ≥18 years who were diagnosed with mCRPC between January 1, 2010 and May 31, 2024 and treated (Cohort 1) or not treated (Cohort 2) with sipuleucel-T in community urology settings. For the preliminary covariates of race, US region, and age and Gleason group scores at diagnosis, patient characteristics were summarized descriptively, Kaplan-Meier (KM) methods and log-rank tests compared OS, and Cox proportional hazards estimated hazard ratios (HRs). Results: Of a total 11,265 men, 46.9% received sipuleucel-T (Cohort 1). Data from the the sipuleucel-T-treated cohort are described in text; all patients are described in the table. Mean age was 73.4 years, 14% were Black, and 46% were in the Southern US region (Table). At PC diagnosis, the mean Gleason score was 7.3, categorizing 53% as high-risk. At mCRPC diagnosis, the mean PSA level was 49.1 ng/mL (median 6.3 ng/mL). Median OS was 44 months (Table). Among the 4,494 patients of cohort 1 with known status, 28% were still alive 5 years after treatment; their median OS was 97 months. Conclusions: Despite their high-risk disease, patients who received sipuleucel-T had a 44-month median OS, with 28% being alive at 5 years later. This highlights the potential therapeutic benefit of integrating sipuleucel-T into real-world treatment for mCRPC. Further analysis is needed, leveraging the rich nature of this dataset. Supported by Dendreon Pharmaceuticals, LLC. Patient characteristics and outcomes. Overall (n=11,265) Cohort 1Sipuleucel-T (n=5,281) Cohort 2No Sipuleucel-T(n=5,984) P -value, Cohort 1 vs 2 Median age, years 76 74 78 <0.001 Race, % (White/Black/Other) 67/15/19 69/14/17 65/15/21 <0.001 US region, % (Midwest/Northeast/South/West) 25/16/45/14 25/16/46/13 26/16/44/14 0.124 PSA at mCRPC diagnosis (mean/median) 81.1/8.0 49.1/6.3 110.0/10.3 <0.001 Gleason score at PC diagnosis, mean 7.3 7.3 7.2 0.064 Alive at 5 years, % 20% 28% 12% <0.001 KM OS (median, 95% CI), months 33 (32, 34) 44 (43, 46) 24 (24, 25) HR (95%CI), Cohort 1 vs 2 1.7 (1.6-1.8)<0.001 CI, confidence interval.

Journal of Clinical OncologyVol. 43(16_suppl)
Dendreon (United States) (US), The Ohio State University Comprehensive Cancer Center – Arthur G. James Cancer Hospital and Richard J. Solove Research Institute (US), Urology of Virginia (US), Michigan Institute of Urology (US), Chesapeake Urology Associates (US), Cardinal Health (United States) (US), Dermatology Specialists (US), Oregon Urology Institute (US), Carolina Urologic Research Center (US), The Ohio State University (US)
Dendreon Pharmaceuticals
Openalex Percentile: Top 80%
Prostate Cancer Treatment and Research
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