Celecoxib recipients had fewer basal cell and squamous cell carcinomas than placebo recipients, but long-term safety is unknown.
In preclinical and epidemiological studies, cyclooxygenase 2 (COX2) has been shown to play a role in the pathogenesis of nonmelanoma skin cancers (NMSCs). Moreover, in animal models, celecoxib (a COX2 inhibitor) has been shown to reduce the formation of ultraviolet-induced premalignant skin papillomas, a murine variant of actinic keratoses. Therefore, investigators conducted a randomized, double-blind, placebo-controlled, phase II–III trial, funded in part by the drug manufacturer, to assess the efficacy of celecoxib in reducing the incidence of actinic keratoses, BCCs, and cutaneous SCCs in 240 high-risk individuals. Eligible patients had 10 to 40 AKs on sun-exposed sites and a prior histological diagnosis of AK, NMSC, or both. Patients re…
Reviewing Author
DisclosuresConsultant / advisory board Lubax; WorldCare Clinical
EquityLubax
Grant / Research support NIH; Department of Defense; American Skin Association; Piramal
Editorial boardsBritish Journal of Dermatology; Journal of the American Academy of Dermatology; Journal of Investigative Dermatology
Leadership positions in professional societies American Academy of Dermatology (Chair, Skin Cancer and Melanoma Committee); American Board of Dermatology (Director)
DisclosuresConsultant / advisory board Lubax; WorldCare Clinical
EquityLubax
Grant / Research support NIH; Department of Defense; American Skin Association; Piramal
Editorial boardsBritish Journal of Dermatology; Journal of the American Academy of Dermatology; Journal of Investigative Dermatology
Leadership positions in professional societies American Academy of Dermatology (Chair, Skin Cancer and Melanoma Committee); American Board of Dermatology (Director)