National patterns of overtreatment in low-risk and undertreatment in high-risk prostate cancer and associated survival impact.

P Pragya Jain (1Baptist Hospitals of Southeast Texas, Beaumont, United States) A Ahmed Abdelhakeem (2Mayo Clinic, Jacksonville, United States) N Nency Ganatra (2Baptist Hospitals of Southeast Texas, Internal Medicine, Beaumont, United States) O Oluwatayo Adeoye (1Mayo Clinic, Hematology/Oncology, Rochester, United States) S Shivam Chetankumar Patel (Baptist Hospitals of Southeast Texas, Beaumont, TX) A Ansy Patel (2SUNY Upstate University, Department of Internal Medicine, Syracuse, United States) M Manan Patel (University of Miami, Miami, FL) J Jakob Skyler Hamilton (Division of Internal Medicine, Mayo Clinic Florida, Jacksonville, FL) A Alicia Hou (Mayo Clinic Florida, Jacksonville, FL) R Ruqin Chen (Division of Hematology and Oncology, Mayo Clinic Florida, Jacksonville, FL) W Winston Tan A Adam McLain Kase (Division of Hematology and Oncology, Mayo Clinic Florida, Jacksonville, FL)

Abstract

e17027 Background: Guidelines recommend active surveillance for low-risk prostate cancer and definitive therapy for high-risk disease. We evaluated national patterns of risk-misaligned care and the survival consequences of undertreatment. Methods: National Cancer Database prostate cancer cases diagnosed from 2010–2022 were analyzed. Low-risk disease was defined as clinical T1–T2, Grade Group 1, and PSA < 10; overtreatment was definitive treatment vs active surveillance or no treatment. High-risk disease was defined as Grade Group ≥4, PSA ≥20, or clinical T3–T4; undertreatment was no definitive local therapy or incomplete definitive therapy. Multivariable logistic regression evaluated factors associated with misalignment. Overall survival (OS) among high-risk patients was assessed using multivariable Cox regression. Results: Among low-risk patients (N = 124,562), overtreatment occurred in 40% of cases. Overtreatment was more common among young men (adjusted odds ratio [aOR] 0.982; p < 0.001) and less common at academic centers (aOR 0.414; p = 0.015). Compared with White men, odds of overtreatment were lower among Black men (aOR 0.946; p = 0.002) and Asian men (aOR 0.827; p < 0.001), with additional variation by education and region (all p < 0.001). Among high-risk patients (N = 318,532), undertreatment affected 27.3% of patients and was more common among older men (aOR 1.061; p < 0.001). Compared with White men, undertreatment was higher among Black men (aOR 1.479; p < 0.001) and lower among Asian patients (aOR 0.863; p < 0.001) (overall race p < 0.001). Compared with private insurance, undertreatment was higher in Medicaid (aOR 2.038; p < 0.001) and uninsured patients (aOR 2.649; p < 0.001), and slightly lower with Medicare (aOR 0.931; p < 0.001) (overall insurance p < 0.001). Multiple comorbidities were associated with higher undertreatment (≥2 vs 0: aOR 1.252; p < 0.001). Facility type was not independently associated (p = 0.490), while region remained significant (overall p < 0.001). In the survival cohort (high risk) (N = 338,919), undertreatment was associated with substantially worse OS (HR 2.745, 95% CI 2.706–2.784; p < 0.001), adjusted for age (HR 1.056; p < 0.001), race (p = 0.001), insurance (p < 0.001), comorbidity (p < 0.001), income (overall p < 0.001), education (overall p < 0.001), and facility region (overall p < 0.001). Conclusions: Low-risk overtreatment remains common nationwide and varies across patient and health-system factors. In high-risk disease, undertreatment affects over one-quarter of patients and disproportionately impacts Black men and those with Medicaid or no insurance. Undertreatment confers a nearly threefold mortality hazard (adjusted HR 2.75; p < 0.001), highlighting a major national quality gap and the urgent need for system-level interventions to ensure equitable, guideline-concordant delivery of definitive therapy.

Article Details

Volume / Issue Vol. 44, Issue 16_suppl
Published June 01, 2026
ISSN 0732-183X
Publisher Lippincott Williams & Wilkins

Journal Info

Journal of Clinical Oncology

Lippincott Williams & Wilkins

ISSN: 0732-183X Health Sciences

Authors (12)

P

Pragya Jain

1Baptist Hospitals of Southeast Texas, Beaumont, United States

A

Ahmed Abdelhakeem

2Mayo Clinic, Jacksonville, United States

N

Nency Ganatra

2Baptist Hospitals of Southeast Texas, Internal Medicine, Beaumont, United States

O

Oluwatayo Adeoye

1Mayo Clinic, Hematology/Oncology, Rochester, United States

S

Shivam Chetankumar Patel

Baptist Hospitals of Southeast Texas, Beaumont, TX

A

Ansy Patel

2SUNY Upstate University, Department of Internal Medicine, Syracuse, United States

M

Manan Patel

University of Miami, Miami, FL

J

Jakob Skyler Hamilton

Division of Internal Medicine, Mayo Clinic Florida, Jacksonville, FL

A

Alicia Hou

Mayo Clinic Florida, Jacksonville, FL

R

Ruqin Chen

Division of Hematology and Oncology, Mayo Clinic Florida, Jacksonville, FL

W

Winston Tan

A

Adam McLain Kase

Division of Hematology and Oncology, Mayo Clinic Florida, Jacksonville, FL