Differential melanoma outcomes in a regional Veterans Affairs center and a tertiary care center with shared physician staffing: A cohort study.
Chen J, Fernandez K, Tang AS, Zhong X, Stewart C, Griffin A, McGuire J, Geisinger L, Grimes B, Wei ML
Journal of the American Academy of DermatologyIn the feed 8 Jul 2026, published online 8 Jul 2026, issue 2026 Jul 08, added to PubMed 8 Jul 2026
Topics: Skin cancer & tumorsMelanoma & moles
Abstract
BACKGROUNDMelanoma outcomes vary by subgroups.
OBJECTIVEIdentify institutional/systemic factors contributing to outcome differences.
METHODSRetrospective cohort study of melanoma patients seen from January 1987 to May 2023 at a Veterans Affairs (VA) center and nearby tertiary care center sharing providers. Outcomes include melanoma-specific survival and mortality.
RESULTSCompared to the tertiary center (n = 9,682, 5564 males), VA patients (n = 638, 612 males) were older and had a greater proportion of melanoma in situ (P < .0001). When comparing VA males to males treated at the tertiary center, melanoma-specific survival was increased for localized melanoma (P = .003) but decreased for regional (P = .0002) and distant disease (P = .02). When comparing VA males to VA-insured males at the tertiary center, melanoma-specific survival remained increased for localized disease (P < .0001), but differences for regional or distant disease were no longer significant. Within the tertiary center, publicly insured patients had increased melanoma-specific mortality compared to privately insured (Medicare, hazard ratio [95% confidence interval]: 1.46 [1.22-1.75]; Medicaid, 1.67 [1.28-2.18]; Military/VA 1.92 [1.15-3.20]).
LIMITATIONSSmaller number of VA-insured patients.
CONCLUSIONDifferences in preventative screening and selective referrals may contribute to increased survival at the VA for early-stage melanoma. Insurance type within and between institutions is associated with differential mortality outcomes for advanced melanoma stages, indicating a need for additional care standardization.
Abstract from PubMed
PMID 42419594 · DOI 10.1016/j.jaad.2026.07.016