Epidemiology of porocarcinoma in England 2013–2018: a population-based registry study

Author:

Joshy Jilse1ORCID,van Bodegraven Birgitta23ORCID,Mistry Khaylen14ORCID,Craig Paul5ORCID,Rajan Neil6ORCID,Vernon Sally3,Levell Nick J14ORCID,Venables Zoe C134ORCID

Affiliation:

1. University of East Anglia, Norwich Medical School , Norwich , UK

2. British Association of Dermatologists , London , UK

3. National Disease Registration Service, Data and Analytics, NHS England , UK

4. Norfolk and Norwich University Hospitals NHS Foundation Trust, Dermatology , Norwich , UK

5. Department of Cellular Pathology, Gloucestershire Hospitals NHS Foundation Trust , Cheltenham , UK

6. Translational and Clinical Research Institute, Newcastle University, Newcastle upon Tyne , UK

Abstract

Abstract Background Porocarcinoma (PC) is a cutaneous malignancy that differentiates towards (possibly arises from) the sweat ducts and glands. Lack of histological diagnostic markers makes clinical and pathological diagnosis complex. The limited data available suggest the incidence is increasing; however, this remains to be established in national epidemiological studies. Objectives To report the incidence, treatment and survival of patients with PC in England from 1 January 2013 to 31 December 2018 using national cancer registry data. Methods PC diagnoses in England during 2013–2018 were identified from the National Disease Registration Service using morphology and behaviour codes. These were registered from routinely collected pathology reports and cancer outcomes and services datasets. The 2013 European age standardized incidence rates (EASRs), Kaplan–Meier all-cause survival and log-rank test were calculated. Results In total, 738 tumours (396 in males and 342 in females) were diagnosed. The median age at diagnosis was 82 years old (interquartile range 74–88). The most frequently affected site were lower limbs (35.4%), followed by the face (16%). The majority of the cohort received surgical excision (73.0%). The Kaplan–Meier all-cause survival was 45.4% at 5 years, which was lower than in previous studies. The EASR for the whole population was 0.25 [95% confidence interval (CI) 0.23–0.27] per 100 000 person-years (PY)]. PC incidence rates in the East of England (EASR of 0.54, 95% CI 0.47–0.63 per 100 000 PY) were three times higher than the South West (EASR of 0.14, 95% CI 0.10–0.19 per 100 000 PY) where the regional rates were the lowest. Conclusions This study shows that there is large variation in the EASRs of PC across England. This may reflect differences in how PC is diagnosed and registered in different regions in England. These data support national assessment of the management of PC, which will inform future studies and guideline development.

Funder

Newcastle NIHR Biomedical Research Centre

Publisher

Oxford University Press (OUP)

Subject

Dermatology

Reference25 articles.

1. Diagnosis and management of porocarcinoma;Miyamoto;Cancers (Basel),2022

2. Demographics and outcomes of eccrine porocarcinoma: results from the National Cancer Database;Behbahani;Br J Dermatol,2020

3. Porocarcinoma; presentation and management, a meta-analysis of 453 cases;Salih AM;Ann Med Surg (Lond),2017

4. Malignant eccrine porocarcinoma in Finland during 2007 to 2017;Meriläinen;Acta Derm Venereol,2021

5. Eccrine porocarcinoma of the skin is rising in incidence in the East of England;Goon;Acta Derm Venereol,2018

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