Evidence map›Paper›PMID 42572578›Full record

ArticleJAAD international2026

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

Charles Lu, Olivia Burke, Christopher J Thang, Sara Khattab, Nga Nguyen, Emma Beagles, Crystal Chang, Suzanne Xu, Jonathan C Hwang, Linden Huhmann and 9 more

Abstract read
In one paragraph

Article in JAAD international, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

19 authors.

Charles LuDepartment of Dermatology, Massachusetts General Hospital, Boston, Massachusetts.
Olivia BurkeDepartment of Dermatology, Massachusetts General Hospital, Boston, Massachusetts.
Christopher J ThangDepartment of Dermatology, Massachusetts General Hospital, Boston, Massachusetts.
Sara KhattabDepartment of Dermatology, Massachusetts General Hospital, Boston, Massachusetts.
Nga NguyenDepartment of Dermatology, Massachusetts General Hospital, Boston, Massachusetts.
Emma BeaglesDepartment of Dermatology, Massachusetts General Hospital, Boston, Massachusetts.
Crystal ChangDepartment of Dermatology, Massachusetts General Hospital, Boston, Massachusetts.
Suzanne XuDepartment of Dermatology, Massachusetts General Hospital, Boston, Massachusetts.
Jonathan C HwangUniversity of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.
Linden HuhmannMassachusetts Veterans Epidemiology Research and Information Center, VA Boston Healthcare System, Boston, Massachusetts.
Nicholas StarinkMelanoma Research Alliance, Washington, District of Columbia.
Martin A WeinstockDepartment of Dermatology, Warren Alpert Medical School, Brown University, Providence, Rhode Island.
Maryam M AsgariDepartment of Dermatology, Massachusetts General Hospital, Boston, Massachusetts.
Marc S HurlbertMelanoma Research Alliance, Washington, District of Columbia.
John M GazianoHarvard Medical School, Boston, Massachusetts.
Nathanael R FillmoreHarvard Medical School, Boston, Massachusetts.
Theodore C FeldmanDermatology Section, VA Boston Healthcare System, Jamaica Plain, Massachusetts.
Rebecca I HartmanHarvard Medical School, Boston, Massachusetts.
Yevgeniy R SemenovDepartment of Dermatology, Massachusetts General Hospital, Boston, Massachusetts.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Acral melanoma (AM) is a rare but aggressive melanoma subtype. Understanding demographic and clinical risk factors is essential for advancing prevention and early detection. Objectives: To identify demographic and clinical risk factors for AM compared with nonmelanoma and cutaneous melanoma (CM) controls. Methods: 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. Results: 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. Conclusions: 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.

Indexed as

acral melanomaepidemiologymedical dermatologymelanomaoncologyskin of color

Identifiers

PMID42572578
PMCPMC13453002

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.