Cutaneous squamous cell carcinoma tumor accrual rates in immunosuppressed patients with autoimmune and inflammatory conditions: A retrospective cohort study.
J Am Acad Dermatol
; 90(4): 731-738, 2024 Apr.
Article
in En
| MEDLINE
| ID: mdl-38043592
ABSTRACT
BACKGROUND:
Immunosuppression is a known risk factor for the development of cutaneous squamous cell carcinoma (CSCC), especially in solid organ transplant recipients and chronic lymphocytic leukemia. However, this risk is less well defined in autoimmune and inflammatory conditions.OBJECTIVE:
Assess the impact that disease-type, duration of immunosuppression, and systemic medications have on CSCC accrual rates, defined as the number of CSCCs a patient develops per year, in autoimmune and inflammatory conditions.METHODS:
Retrospective review of 94 immunosuppressed (rheumatoid arthritis 31[33.0%], inflammatory bowel disease 17[18.1%], psoriasis 11[11.7%], autoimmune other (AO) 24[25.5%], inflammatory other 21[22.3%]) and 188 immunocompetent controls to identify all primary, invasive CSCCs diagnosed from 2010 to 2020.RESULTS:
Immunosuppressed patients had higher CSCC accrual rates than immunocompetent controls (0.44 ± 0.36) total cohort (0.82 ± 0.95, P < .01), rheumatoid arthritis (0.88 ± 1.10, P < .01), inflammatory bowel disease (0.94 ± 0.88, P < .01), psoriasis (1.06 ± 1.58, P < .01), AO (0.72 ± 0.56, P < .01), and inflammatory other (0.72 ± 0.61, P < .01). There was an association between increased tumor accrual rates and exposure to systemic medications including, immunomodulators, tumor necrosis factor-alpha inhibitors, non-tumor necrosis factor inhibitor biologics, and corticosteroids, but not with number of systemic medication class exposures or duration of immunosuppression.LIMITATIONS:
Retrospective, singlecenter study.CONCLUSION:
Patients with autoimmune and inflammatory conditions accrue CSCCs at higher rates than immunocompetent patients.Key words
Full text:
1
Database:
MEDLINE
Main subject:
Arthritis, Rheumatoid
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Psoriasis
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Skin Neoplasms
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Carcinoma, Squamous Cell
/
Inflammatory Bowel Diseases
Limits:
Humans
Language:
En
Journal:
J Am Acad Dermatol
Year:
2024
Type:
Article