Clinical outcomes among patients with metastatic hormone-sensitive prostate cancer in contemporary real-world US clinical practice: A prostate cancer disease observation (PRECISION) data platform analysis.

A Alton Oliver Sartor (LCMC Health, New Orleans, LA) E Elisabeth I. Heath (Department of Medical Oncology, Mayo Clinic Rochester, Rochester, MN) N Neal D. Shore (START Carolinas/Carolina Urologic Research Center, Myrtle Beach, SC) X Xiao X. Wei (Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA) J Jennifer Nguyen (Department of Chemistry) J Jeetvan Patel (Novartis Pharmaceuticals Corporation, East Hanover, NJ) D Diego Ospina Gonzalez (Novartis Pharmaceuticals Corporation, East Hanover, NJ) B Barinder Kang (Novartis Pharmaceuticals Corporation, East Hanover, NJ) C Clare Byrne (Asclepius Analytics, New York, NY) J Jackson Tang (Asclepius Analytics, New York, NY) D Daniel J. George (Duke Cancer Institute, Duke University School of Medicine, Durham, NC)

Abstract

77 Background: The incidence of metastatic hormone-sensitive prostate cancer (mHSPC) is increasing in the US, likely due to a decrease in screening practices. There has also been a rapid increase in recent years in the number of treatment options that can improve progression-free and overall survival (OS) for these patients. The objective of the current study was to evaluate the clinical outcomes among patients with mHSPC treated in contemporary US clinical practice (2020 to 2025). Methods: This retrospective, observational cohort study used data from PRECISION, a harmonized dataset on advanced prostate cancer in patients in the US treated in a range of clinical settings. Patients aged ≥18 years who were diagnosed with mHSPC during 01/01/2020–01/01/2024 and who initiated ≥1 therapy (index date = first-line [1L] treatment initiation) were included. The study period was from 01/01/2010 to 06/30/2025. Patient characteristics at mHSPC diagnosis and treatment utilization were evaluated descriptively. Castration resistance-free survival (CRFS; defined as the time to castration-resistant prostate cancer or death) and OS were evaluated from index using Kaplan–Meier analysis. Results: A total of 27,708 patients were included (median age, 72 years); 20,015 (72%) were treated in community urology, 4994 (18%) in community oncology, and 2669 (10%) in academic oncology centers at index. Almost half of patients (47%) initiated 1L treatment with androgen-deprivation therapy (ADT) monotherapy, 44% initiated a 1L doublet regimen (36% ADT + androgen receptor pathway inhibitor [ARPI], 5% 1L ADT + radiotherapy, 2% 1L ADT + docetaxel), and 5% a 1L triplet regimen (ADT + radiotherapy + ARPI or docetaxel); the remaining patients received other regimens. The 5-year CRFS rate was 41%; this was significantly higher in patients with a 1L doublet (45%) or triplet (58%) regimen compared with patients with 1L ADT monotherapy (31%; p<0.001). Similarly, the 5-year OS rate was 59% overall and was significantly higher in patients with a 1L doublet (61%) or triplet (59%) regimen compared with patients with 1L ADT monotherapy (55%; p<0.001) (Table). Conclusions: Though both CRFS and OS rates appear to be increasing among real-world patients with mHSPC, >40% of patients in this study died within 5 years of initiating 1L treatment. Patients who received guideline-recommended combined systemic treatment regimens experienced improved CRFS and OS, confirming the importance of implementing therapies in practice that prolong survival. CRFS and OS rates from start of 1L therapy, by therapy type. CRFS rate (%) OS rate (%) 1 y 2 y 3 y 4 y 5 y 1 y 2 y 3 y 4 y 5 y Overall 68 58 51 46 41 93 84 76 67 59 ADT monotherapy 59 49 41 36 31 92 83 74 65 55 Doublet therapy 72 62 55 49 45 94 85 76 68 61 Triplet therapy 85 77 70 68 58 94 89 82 74 59

Article Details

Volume / Issue Vol. 44, Issue 7_suppl
Published March 01, 2026
Pages 77-77
ISSN 0732-183X
Publisher Lippincott Williams & Wilkins

Journal Info

Journal of Clinical Oncology

Lippincott Williams & Wilkins

ISSN: 0732-183X Health Sciences

Authors (11)

A

Alton Oliver Sartor

LCMC Health, New Orleans, LA

E

Elisabeth I. Heath

Department of Medical Oncology, Mayo Clinic Rochester, Rochester, MN

N

Neal D. Shore

START Carolinas/Carolina Urologic Research Center, Myrtle Beach, SC

X

Xiao X. Wei

Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA

J

Jennifer Nguyen

Department of Chemistry

J

Jeetvan Patel

Novartis Pharmaceuticals Corporation, East Hanover, NJ

D

Diego Ospina Gonzalez

Novartis Pharmaceuticals Corporation, East Hanover, NJ

B

Barinder Kang

Novartis Pharmaceuticals Corporation, East Hanover, NJ

C

Clare Byrne

Asclepius Analytics, New York, NY

J

Jackson Tang

Asclepius Analytics, New York, NY

D

Daniel J. George

Duke Cancer Institute, Duke University School of Medicine, Durham, NC