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Review
. 2019 Apr 15;25(8):2379-2391.
doi: 10.1158/1078-0432.CCR-18-1122. Epub 2018 Dec 6.

Keratinocyte Carcinomas: Current Concepts and Future Research Priorities

Affiliations
Review

Keratinocyte Carcinomas: Current Concepts and Future Research Priorities

Priyadharsini Nagarajan et al. Clin Cancer Res. .

Abstract

Cutaneous squamous cell carcinoma (cSCC) and basal cell carcinoma (BCC) are keratinocyte carcinomas, the most frequently diagnosed cancers in fair-skinned populations. Ultraviolet radiation (UVR) is the main driving carcinogen for these tumors, but immunosuppression, pigmentary factors, and aging are also risk factors. Scientific discoveries have improved the understanding of the role of human papillomaviruses (HPV) in cSCC as well as the skin microbiome and a compromised immune system in the development of both cSCC and BCC. Genomic analyses have uncovered genetic risk variants, high-risk susceptibility genes, and somatic events that underlie common pathways important in keratinocyte carcinoma tumorigenesis and tumor characteristics that have enabled development of prediction models for early identification of high-risk individuals. Advances in chemoprevention in high-risk individuals and progress in targeted and immune-based treatment approaches have the potential to decrease the morbidity and mortality associated with these tumors. As the incidence and prevalence of keratinocyte carcinoma continue to increase, strategies for prevention, including effective sun-protective behavior, educational interventions, and reduction of tanning bed access and usage, are essential. Gaps in our knowledge requiring additional research to reduce the high morbidity and costs associated with keratinocyte carcinoma include better understanding of factors leading to more aggressive tumors, the roles of microbiome and HPV infection, prediction of response to therapies including immune checkpoint blockade, and how to tailor both prevention and treatment to individual risk factors and needs.

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Conflict of interest statement

Potential Conflicts of Interest: M. M. Asgari reports receiving commercial research grants from Pfizer and Valeant. S. T. Arron reports receiving other commercial research support (paid directly to UCSF) from Leo Pharma, SunPharma, Menlo Therapeutics, Castle Biosciences, Genentech/Roche, Pfizer, Regeneron, Eli Lilly, and PellePharm, is a consultant for Enspectra Health, Regeneron, Sanofi-Genzyme, Castle Creek Pharmaceuticals, SunPharma, Pennside Partners, Biossance, Gerson Lehrman Group, and Rakuten Aspyrian, and holds ownership interest in Genentech. C. A. Harwood reports receiving other commercial research support from MEDA and Pellepharm, speakers bureau honoraria from Sanofi, and is a consultant/advisory board member for Novartis. No potential conflicts of interest were disclosed by the other authors.

Figures

Figure 1:
Figure 1:. Unique and shared risk factors for BCC and cSCC
Intrinsic and extrinsic risk factors for the development of BCC and cSCC are shown including factors that are in common or unique to each tumor type.
Figure 2:
Figure 2:. Areas of Research Need
Some of the clinical and scientific areas in need of additional research to drive improvements in KC understanding, prevention, treatment, and outcomes are highlighted. IS, immunosuppression; SOTR, solid organ transplant recipients; RTR, renal transplant recipients.

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