Hospital volume, travel burden, and survival disparities in stage IV melanoma: A U.S. national cohort.

K Katiuscha Merath (Saint John's Cancer Institute, Santa Monica, CA) D Douglas A. Hanes (Providence Cancer Institute, Portland, OR) H Hilary Keller (Saint John's Cancer Institute, Santa Monica, CA) B Brian Diskin (Saint John's Cancer Institute, Santa Monica, CA) S Sia Bolourani (Saint John's Cancer Institute, Santa Monica, CA) N Nicholas Ullman (Saint John's Cancer Institute, Santa Monica, CA) M Melanie Goldfarb R Richard Essner (John Wayne Cancer Institute at Saint John's Hospital; California Oncology Research I, Santa Monica, CA)

Abstract

e21597 Background: Advances in immunotherapy and selective surgical resection have improved outcomes for stage IV melanoma, yet access to high-quality multidisciplinary care might not be possible for all patients. High-volume centers (HVCs) may deliver more guideline-concordant treatment but often require long-distance travel, raising concerns about socioeconomic and racial inequities. We evaluated the association of hospital volume and travel distance with treatment patterns, survival, and equity in stage IV melanoma. Methods: Patients with AJCC stage IV melanoma diagnosed between 2014–2022 were identified from the National Cancer Database. Hospitals were categorized by annual invasive melanoma volume as low (< 35/year), medium (35–91/year), or high ( > 91/year). Patients in the lowest travel-distance quartile treated at low-volume centers (Local-LVC) were compared with those in the highest travel-distance quartile treated at HVCs (Travel-HVC). Overall survival (OS) was analyzed using Kaplan–Meier methods and multivariable Cox regression adjusting for demographics, insurance, comorbidity, metastatic site, facility characteristics, and treatment. Results: Median travel distance ranged from 4.9–9.9 miles for Local-LVC patients versus 25.3–64 miles for Travel-HVC patients, varying by region. Travel-HVC patients were more likely to be White, privately insured, and treated at academic centers, and more frequently received first-line immunotherapy (75.9% vs 63.5%) and immunotherapy followed by surgery (44% vs 32%) (all p < 0.001). On multivariable analysis, treatment at a Travel-HVC was independently associated with improved OS compared with Local-LVC care (HR 0.80, 95% CI 0.67–0.95; p = 0.012). Immunotherapy alone (HR 0.72, 95% CI 0.62–0.82) and immunotherapy plus surgery (HR 0.48, 95% CI 0.42–0.56) were associated with superior OS compared with surgery alone (both p < 0.001). Brain metastases (HR 2.02), lung metastases (HR 1.42), and metastases to > 1 site (HR 2.66) were associated with worse survival (all p ≤0.05), yet the survival benefit of Travel-HVC care persisted across metastatic patterns and treatment strategies. Lack of insurance (HR 1.34) and Medicaid/government insurance (HR 1.37) were independently associated with worse OS, while racial disparities observed on unadjusted analysis were attenuated after adjustment for insurance and care delivery factors. Conclusions: Access to high-volume centers was independently associated with improved survival for patients with stage IV melanoma, even after accounting for treatment modality, disease burden, and socioeconomic factors. These findings suggest that structural access to high-quality multidisciplinary care—rather than race alone—drives much of the observed survival disparity and support regional referral pathways and shared-care models to promote equity in advanced melanoma care.

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 (8)

K

Katiuscha Merath

Saint John's Cancer Institute, Santa Monica, CA

D

Douglas A. Hanes

Providence Cancer Institute, Portland, OR

H

Hilary Keller

Saint John's Cancer Institute, Santa Monica, CA

B

Brian Diskin

Saint John's Cancer Institute, Santa Monica, CA

S

Sia Bolourani

Saint John's Cancer Institute, Santa Monica, CA

N

Nicholas Ullman

Saint John's Cancer Institute, Santa Monica, CA

M

Melanie Goldfarb

R

Richard Essner

John Wayne Cancer Institute at Saint John's Hospital; California Oncology Research I, Santa Monica, CA