Impact of guideline-discordant care for muscle-invasive bladder cancer on preventable survival losses: A national counterfactual analysis of 55,873 patients.

S Shivam Chetankumar Patel (Baptist Hospitals of Southeast Texas, Beaumont, TX) P Pragya Jain (1Baptist Hospitals of Southeast Texas, Beaumont, United States) A Ansy Patel (2SUNY Upstate University, Department of Internal Medicine, Syracuse, United States) V Vedant Shah (NYMC St Mary and St Clare Health, Parsippany-Troy Hills, New Jersey, United States) K Krima Patel (1Baptist Hospitals of Southeast Texas, Internal Medicine, Beaumont, United States) N Nency Ganatra (2Baptist Hospitals of Southeast Texas, Internal Medicine, Beaumont, United States) J Junaid Anwar (3MD ANDERSON CANCER CENTER, Houston, United States) A Ahmed Abdelhakeem (2Mayo Clinic, Jacksonville, United States) A Amit Correa (3MD ANDERSON CANCER CENTER, Houston, United States) T Tahir A. Naqvi (Baptist Hospitals of Southeast Texas, Beaumont, TX)

Abstract

e16586 Background: Guideline-discordant care disproportionately affects racial minorities, uninsured, and underinsured patients, yet prior studies lack quantification of absolute survival time lost. We evaluated equity-adjusted survival penalties from non-adherence to guideline-concordant therapy in muscle-invasive bladder cancer (MIBC). Methods: From the National Cancer Database, we identified patients with non metastatic muscle invasive bladder cancer (cT2 to T4a, N0 or N1, M0). Overall survival was defined from diagnosis to death or last contact. Guideline-concordant therapy was defined as radical cystectomy (± perioperative systemic therapy) or trimodality therapy (definitive bladder radiotherapy with chemotherapy); all other patterns were classified as discordant. Of 55,873 eligible patients, 28,025 received concordant therapy (27,401 cystectomy; 524 trimodality therapy) and 27,848 received discordant careInverse probability of treatment weighting (IPTW) was used to balance demographic, socioeconomic, facility, tumor, and temporal covariates. We analyzed survival using weighted Kaplan-Meier and Cox models censored at 36 and 60 months. Equity-adjusted survival penalties were calculated as the difference between observed survival and counterfactual survival predicted from concordant-only models. Restricted mean survival time losses were extrapolated to years lost per 1,000 patients. Results: Guideline concordance was associated with significantly improved survival (36-month HR 0.64; 60-month HR 0.68; both p < 0.01). Among concordant modalities, radical cystectomy conferred an early survival advantage over trimodality therapy at 36 months (HR 0.23; p < 0.05) which dissipated by 60 months (HR 0.53; p > 0.05). Survival penalties were most severe for vulnerable populations. At 36 months, uninsured patients incurred a 0.90-month survival penalty (75.0 life-years lost per 1,000 patients). By 60 months, penalties widened: uninsured patients lost 1.94 months (161.7 life-years/1,000), Filipino patients lost 1.53 months (127.0/1,000), Medicaid beneficiaries lost 0.97 months (80.8/1,000), and patients at community cancer programs lost 0.21 months (54.1/1,000). Conclusions: In this national cohort of 55,873 patients, guideline concordance reduced the propensity-weighted risk of death by 32% to 36% at 3 and 5 years. However, non-adherence results in substantial absolute survival losses for marginalized groups. By quantifying these "survival penalties," we demonstrate that targeting the factors underlying discordance offers a direct opportunity to reduce inequities and achieve measurable population-level survival gains in MIBC.

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 (10)

S

Shivam Chetankumar Patel

Baptist Hospitals of Southeast Texas, Beaumont, TX

P

Pragya Jain

1Baptist Hospitals of Southeast Texas, Beaumont, United States

A

Ansy Patel

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

V

Vedant Shah

NYMC St Mary and St Clare Health, Parsippany-Troy Hills, New Jersey, United States

K

Krima Patel

1Baptist Hospitals of Southeast Texas, Internal Medicine, Beaumont, United States

N

Nency Ganatra

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

J

Junaid Anwar

3MD ANDERSON CANCER CENTER, Houston, United States

A

Ahmed Abdelhakeem

2Mayo Clinic, Jacksonville, United States

A

Amit Correa

3MD ANDERSON CANCER CENTER, Houston, United States

T

Tahir A. Naqvi

Baptist Hospitals of Southeast Texas, Beaumont, TX