Delayed Time to First Skin Cancer Among Hematopoietic Stem Cell Transplant Recipients With Chronic Cutaneous Graft‐Versus‐Host Disease

ABSTRACT Background Hematopoietic stem cell transplant (HSCT) recipients face an increased risk of cutaneous malignancies. Chronic cutaneous graft‐versus‐host disease (cGVHD), specific to allogeneic HSCT (alloHSCT), has been proposed to further elevate this risk, though its impact on skin cancer latency and distribution remains unclear. Objectives To evaluate the timeline and characteristics of post‐transplant skin cancers in HSCT recipients, stratified by transplant type and presence of cutaneous cGVHD. Methods A retrospective cohort study of HSCT recipients with documented cutaneous malignancies treated at Duke University Medical Center from 2010 to 2020. Patients with solid organ transplants were excluded. Primary outcomes were time to first and second skin cancer post‐transplant. Secondary outcomes included cancer type, number, and anatomic location. Results Among 192 patients, 96 underwent alloHSCT with cutaneous cGVHD, 20 alloHSCT without cGVHD, and 76 autoHSCT. Time to first skin cancer was significantly longer in the cGVHD group (mean 2131 days) compared to alloHSCT without cGVHD (1686 days) and autoHSCT (1287 days; p = 0.047). However, time to second malignancy was shorter in the cGVHD cohort (2871 days) than in alloHSCT without cGVHD (4231 days) but longer than autoHSCT recipients (1954 days; p = 0.02). SCC was the most prevalent malignancy, though patients with cGVHD had higher rates of BCC and melanoma. Cutaneous cancers predominantly involved UV‐exposed areas, but truncal involvement was more common in cGVHD patients. Conclusions HSCT recipients with cutaneous cGVHD demonstrate delayed onset of first skin cancer but accelerated development of subsequent malignancies. These findings suggest dynamic immune shifts over time and emphasize the need for tailored dermatologic surveillance protocols based on transplant type and cGVHD status.

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Publication Details

Journal
JEADV Clinical Practice
Published
2025-10-15
DOI
https://doi.org/10.1002/jvc2.70195
Primary Topic
Nonmelanoma Skin Cancer Studies
Type
article
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article

Delayed Time to First Skin Cancer Among Hematopoietic Stem Cell Transplant Recipients With Chronic Cutaneous Graft‐Versus‐Host Disease

Vanessa J Lazaro-Camp, Melodi Javid Whitley, Amy J. Petty
JEADV Clinical Practice
Nonmelanoma Skin Cancer Studies
article

Delayed Time to First Skin Cancer Among Hematopoietic Stem Cell Transplant Recipients With Chronic Cutaneous Graft‐Versus‐Host Disease

Vanessa J Lazaro-Camp, Melodi Javid Whitley, Amy J. Petty
article en

Abstract

ABSTRACT Background Hematopoietic stem cell transplant (HSCT) recipients face an increased risk of cutaneous malignancies. Chronic cutaneous graft‐versus‐host disease (cGVHD), specific to allogeneic HSCT (alloHSCT), has been proposed to further elevate this risk, though its impact on skin cancer latency and distribution remains unclear. Objectives To evaluate the timeline and characteristics of post‐transplant skin cancers in HSCT recipients, stratified by transplant type and presence of cutaneous cGVHD. Methods A retrospective cohort study of HSCT recipients with documented cutaneous malignancies treated at Duke University Medical Center from 2010 to 2020. Patients with solid organ transplants were excluded. Primary outcomes were time to first and second skin cancer post‐transplant. Secondary outcomes included cancer type, number, and anatomic location. Results Among 192 patients, 96 underwent alloHSCT with cutaneous cGVHD, 20 alloHSCT without cGVHD, and 76 autoHSCT. Time to first skin cancer was significantly longer in the cGVHD group (mean 2131 days) compared to alloHSCT without cGVHD (1686 days) and autoHSCT (1287 days; p = 0.047). However, time to second malignancy was shorter in the cGVHD cohort (2871 days) than in alloHSCT without cGVHD (4231 days) but longer than autoHSCT recipients (1954 days; p = 0.02). SCC was the most prevalent malignancy, though patients with cGVHD had higher rates of BCC and melanoma. Cutaneous cancers predominantly involved UV‐exposed areas, but truncal involvement was more common in cGVHD patients. Conclusions HSCT recipients with cutaneous cGVHD demonstrate delayed onset of first skin cancer but accelerated development of subsequent malignancies. These findings suggest dynamic immune shifts over time and emphasize the need for tailored dermatologic surveillance protocols based on transplant type and cGVHD status.

JEADV Clinical PracticeVol. 5(1)
Duke University (US)
Openalex Percentile: Top 61%
Nonmelanoma Skin Cancer Studies
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