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Risk factors for the development of acral melanoma: A multi-institutional, retrospective cohort study.

Created on 10 Aug 2026

Authors

Charles Lu, Olivia Burke, Christopher J Thang, Sara Khattab, Nga Nguyen, Emma Beagles, Crystal Chang, Suzanne Xu, Jonathan C Hwang, Linden Huhmann, Nicholas Starink, Martin A Weinstock, Maryam M Asgari, Marc S Hurlbert, John M Gaziano, Nathanael R Fillmore, Theodore C Feldman, Rebecca I Hartman, Yevgeniy R Semenov

Published in

JAAD international. Volume 28. Pages 38-46. Epub May 29, 2026.

Abstract

Acral melanoma (AM) is a rare but aggressive melanoma subtype. Understanding demographic and clinical risk factors is essential for advancing prevention and early detection.
To identify demographic and clinical risk factors for AM compared with nonmelanoma and cutaneous melanoma (CM) controls.
This multi-institutional retrospective cohort study of patients evaluated at the Mass General Brigham and Dana-Farber Cancer Institute. Three cohorts were created via manual curation of pathology reports: AM cases, nonmelanoma controls, and CM controls. AM patients were matched 1:4 to controls based on pre/postindex follow-up time and dermatologic care history. Multivariable logistic regression and structural equation modeling assessed direct and indirect pathways linking sex, actinic keratoses, and melanoma subtype.
A total of 2115 patients were analyzed. AM patients were more often female and disproportionately Asian or Black compared with both controls. Relative to non-melanoma controls, AM was associated with female sex, Asian, or Black race, leukemia/lymphoma, nonmelanoma skin cancer, and actinic keratoses. Similar findings were present against CM controls.
AM risk is associated with female sex, Asian or Black race, and select prior malignancies. Findings demonstrate an association between markers of UV exposure (actinic keratoses) and AM risk, though significantly weaker than in CM. These insights may guide prevention, risk stratification, and mechanistic research.

PMID:
42572578
Bibliographic data and abstract were imported from PubMed on 10 Aug 2026.

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