Clinical Features and Outcomes of Black Patients With Melanoma
Clinical Summary
View sourceWhat was studied
A single‑institution case series of 48 self‑reported Black patients with histopathology‑proven melanoma seen at two tertiary centers in Dallas from January 2006 to October 2022, assessing demographics, anatomic site, histology, immune status, treatments, genomics, progression, and survival.
Key findings
Of 40 primary cutaneous melanomas, 30 (75%) occurred on acral skin, yet only 10/30 (33%) were histologic acral lentiginous melanomas; nonacral cutaneous cases were more often immunocompromised (4/10 [40%] vs 2/30 [7%]) and had a personal cancer history (6/10 [60%] vs 5/30 [17%]). Overall, 13/48 (27%) developed stage IV disease and 12 died of progression; advanced acral, mucosal/ocular, or unknown‑primary melanomas lacked actionable variants, were nonresponsive to immunotherapy, and had the worst outcomes, while no nonacral cutaneous melanomas developed distant metastases or melanoma deaths.
Study limitations
Single‑institution case series with small sample size (n=48) from two tertiary centers. Key clinicopathologic data were often missing (e.g., Breslow depth not determined in 21/48 [44%]), and molecular testing was limited to subsets (e.g., BRAF tested in 16).
Clinical implications
In this series, melanoma in Black patients most often arose on acral sites, and advanced acral, mucosal/ocular, and unknown‑primary cases had poor outcomes with little immunotherapy response; nonacral cutaneous cases did not metastasize or die of melanoma. Nonacral cutaneous melanomas were frequently linked with immunosuppression and prior cancer history in this cohort.
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