Abstract

SummaryBackgroundBasal cell carcinoma (BCC) and cutaneous squamous cell carcinoma (cSCC), together known as keratinocyte cancers (KCs), are the commonest cancer in white ethnic populations. Recent improvements to registry data collection in England has allowed more accurate analysis of the epidemiology of BCC and cSCC and for the first time we are able to provide an accurate (representative) tumour burden for KC in the U.K.ObjectivesTo estimate the incidence of BCC and cSCC in the U.K.MethodsA cohort of patients with KCs between 2013 and 2015 were identified using linkage to diagnostic codes derived from pathology reports collected into the national cancer registry. Data from England's cancer registry were combined with data from Scotland, Northern Ireland and Wales. European age‐standardized incidence rates (EASRs) of the first BCC and cSCC per patient per annum (PPPA) were calculated.ResultsIn the U.K, the EASR of the first BCC and cSCC PPPA in 2013–15 were 285 and 77 per 100 000 person years, respectively (211 120 KCs total in 2015). The mean annual percentage increase was 5% between 2013 and 2015 for both BCC and cSCC. By counting the first KC PPPA, we include an additional 51% KCs compared with the previous reporting technique which counts only the first BCC and cSCC in a patient's lifetime, yet it represents a probable underestimation of 5–11% of the true tumour count.ConclusionsBased on an improved methodology, a more representative incidence of KC is presented, which is essential to healthcare planning and will lead to improved understanding of the epidemiology of KC. What's already known about this topic? Keratinocyte cancers (KCs) are the most common cancers affecting white ethnic populations.The incidence of basal cell carcinoma (BCC) and cutaneous squamous cell carcinoma (cSCC) is increasing worldwide including the U.K., most commonly in elderly male Caucasian patients.These cancers are traditionally substantially underreported and frequently excluded from national cancer statistics. What does this study add? Using improved data collection methods in England and validated tumour‐reporting techniques, we report the most accurate BCC and cSCC incidence data for the U.K. ever published.Identifying the first BCC and cSCC per patient per annum, the incidence of BCC and cSCC in the U.K. (excluding Wales) was 285 and 77 per 100 000 person years, respectively, between 2013 and 2015, with more than 210 000 KCs in the U.K. in 2015.

Highlights

  • Keratinocyte cancers (KCs), the collective term for basal cell carcinomas (BCCs) and cutaneous squamous cell carcinomas, are the most common cancers in the UK and the most common cancer in white ethnic populations worldwide

  • By counting the first tumour per patient per year, we include an additional 51% keratinocyte cancers (KCs) compared to the previous reporting technique which counts only the first BCC and cutaneous squamous cell carcinoma (cSCC) in a patient’s lifetime, yet it represents a probable underestimation of 5-11% of the true tumour count

  • Based on an improved methodology, a more representative incidence of KC is presented, which is essential to healthcare planning and will lead to improved understanding of the epidemiology of KC

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Summary

Introduction

Keratinocyte cancers (KCs), the collective term for basal cell carcinomas (BCCs) and cutaneous squamous cell carcinomas (cSCCs), are the most common cancers in the UK and the most common cancer in white ethnic populations worldwide. Increasing tumour incidence is presumed to be a result of an ageing population, increased ultraviolet (UV) radiation exposure with easier access to travel abroad and a higher proportion of fairer skin types in the UK compared to other countries, [6, 14] but little is known about the epidemiology of KC in the UK. Basal cell carcinoma (BCC) and cutaneous squamous cell carcinoma (cSCC), together known as keratinocyte cancers (KCs), are the commonest cancer in Caucasian populations. Recent improvements to registry data collection in England has allowed more accurate analysis of the epidemiology of BCC and cSCC and for the first time we are able to provide an accurate (representative) tumour burden for KC in the UK

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