Primary liver cancer in the UK: Incidence, incidence-based mortality, and survival by subtype, sex, and nation.

AAPC, average annual percentage change APC, annual percentage change ASMR, age-standardised mortality rate ASR, age-standardised incidence rate BASL, British Association for the Study of the Liver DAA, direct-acting antivirals DCO, death certificate only HCC, hepatocellular carcinoma HCV, hepatitis C virus Hepatocellular carcinoma ICCA, intrahepatic cholangiocarcinoma ICD-10, International Classification of Diseases 10th Edition ICD-O, International Classification of Diseases for Oncology Incidence Intrahepatic cholangiocarcinoma Mortality NAFLD, non-alcoholic fatty liver disease NCRAS, National Cancer Registration and Analysis Service NI, Northern Ireland PLC, primary liver cancer Primary liver cancer Survival

Journal

JHEP reports : innovation in hepatology
ISSN: 2589-5559
Titre abrégé: JHEP Rep
Pays: Netherlands
ID NLM: 101761237

Informations de publication

Date de publication:
Apr 2021
Historique:
received: 11 10 2020
revised: 22 12 2020
accepted: 06 01 2021
entrez: 22 3 2021
pubmed: 23 3 2021
medline: 23 3 2021
Statut: epublish

Résumé

The incidence of primary liver cancer (PLC) is increasing in Western Europe. To understand trends over time and the current burden in the UK, a detailed analysis of the epidemiology of PLC and its subtypes was conducted. Data on PLCs diagnosed during 1997-2017 were obtained from population-based, nationwide registries in the UK. European age-standardised incidence (ASR) and incidence-based mortality rates (ASMR) per 100,000 person-years were calculated overall and by sex and UK-nation. Annual percentage change in rates was estimated using Joinpoint regression. One-, 2-, and 5-year age-standardised net survival was estimated. A total of 82,024 PLCs were diagnosed. Both hepatocellular carcinoma (HCC) incidence and mortality rates trebled (ASR 1.8-5.5 per 100,000, ASMR 1.3-4.0). The rate of increase appeared to plateau around 2014/2015. Scottish men consistently had the highest HCC incidence rates. PLC survival increased, driven by a substantial increase in the proportion that are HCC (as prognosis is better than other PLCs) and in HCC survival (change in 1-year survival 24-47%). Intrahepatic cholangiocarcinoma was the most common PLC in women and 1-year survival improved from 22.6% to 30.5%. PLC incidence has been increasing rapidly but, as most risk factors are modifiable, it is largely a preventable cancer. This rate of increase has slowed in recent years, possibly attributable to effective treatment for hepatitis C. As other risk factors such as obesity and diabetes remain prevalent in the UK, it is unlikely the considerable burden of this disease will abate. While improvements in survival have been made, over half of patients are not alive after 1 year, therefore further progress in prevention, early detection, and treatment innovation are needed. Many more people are getting liver cancer, particularly the subtype hepatocellular carcinoma, than 20 years ago. Men in Scotland are most likely to get liver cancer and to die from it. Survival after liver cancer diagnosis is getting longer but still less than half are alive after 1 year.

Sections du résumé

BACKGROUND & AIMS OBJECTIVE
The incidence of primary liver cancer (PLC) is increasing in Western Europe. To understand trends over time and the current burden in the UK, a detailed analysis of the epidemiology of PLC and its subtypes was conducted.
METHODS METHODS
Data on PLCs diagnosed during 1997-2017 were obtained from population-based, nationwide registries in the UK. European age-standardised incidence (ASR) and incidence-based mortality rates (ASMR) per 100,000 person-years were calculated overall and by sex and UK-nation. Annual percentage change in rates was estimated using Joinpoint regression. One-, 2-, and 5-year age-standardised net survival was estimated.
RESULTS RESULTS
A total of 82,024 PLCs were diagnosed. Both hepatocellular carcinoma (HCC) incidence and mortality rates trebled (ASR 1.8-5.5 per 100,000, ASMR 1.3-4.0). The rate of increase appeared to plateau around 2014/2015. Scottish men consistently had the highest HCC incidence rates. PLC survival increased, driven by a substantial increase in the proportion that are HCC (as prognosis is better than other PLCs) and in HCC survival (change in 1-year survival 24-47%). Intrahepatic cholangiocarcinoma was the most common PLC in women and 1-year survival improved from 22.6% to 30.5%.
CONCLUSIONS CONCLUSIONS
PLC incidence has been increasing rapidly but, as most risk factors are modifiable, it is largely a preventable cancer. This rate of increase has slowed in recent years, possibly attributable to effective treatment for hepatitis C. As other risk factors such as obesity and diabetes remain prevalent in the UK, it is unlikely the considerable burden of this disease will abate. While improvements in survival have been made, over half of patients are not alive after 1 year, therefore further progress in prevention, early detection, and treatment innovation are needed.
LAY SUMMARY BACKGROUND
Many more people are getting liver cancer, particularly the subtype hepatocellular carcinoma, than 20 years ago. Men in Scotland are most likely to get liver cancer and to die from it. Survival after liver cancer diagnosis is getting longer but still less than half are alive after 1 year.

Identifiants

pubmed: 33748727
doi: 10.1016/j.jhepr.2021.100232
pii: S2589-5559(21)00008-2
pmc: PMC7966867
doi:

Types de publication

Journal Article

Langues

eng

Pagination

100232

Subventions

Organisme : Cancer Research UK
ID : 26813
Pays : United Kingdom
Organisme : Chief Scientist Office
ID : CGA/17/19
Pays : United Kingdom

Investigateurs

Anya Burton (A)
Aileen Marshall (A)
Graeme Alexander (G)
Ian Rowe (I)
Robert J Driver (RJ)
Vinay Kumar (V)
Tim Cross (T)
Katherine Cullen (K)
Rhys Pockett (R)
Tom Bird (T)
Dyfed W Huws (DW)
Anna Gavin (A)
Daniela Tataru (D)
Lizz Paley (L)
David Wallace (D)
Guruprasad Aithal (G)

Informations de copyright

Crown Copyright © 2021 Published by Elsevier B.V. on behalf of European Association for the Study of the Liver (EASL).

Déclaration de conflit d'intérêts

All of the authors completed the ICMJE uniform disclosure form; GA, AM, DT, DH, DW, TGB, and RJD have nothing to disclose. During the conduct of the study, AB reports grants from BTG International Ltd. Outside of the submitted work TJSC reports grants from Sirtex, Bristol-Myers-Squibb, and Bayer and personal fees from Eisai pharmaceuticals, Bayer, AstraZeneca, and Roche. IAR reports personal fees from Roche and Abbvie, outside the submitted work. Please refer to the accompanying ICMJE disclosure forms for further details.

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Auteurs

Anya Burton (A)

HCC-UK/British Association for the Study of the Liver (BASL), Lichfield, UK.
National Cancer Registration and Analysis Service, National Disease Registration Service, Public Health England, London, UK.

Daniela Tataru (D)

National Cancer Registration and Analysis Service, National Disease Registration Service, Public Health England, London, UK.

Robert J Driver (RJ)

Leeds Institute for Medical Research at St. James's, University of Leeds, Leeds, UK.

Thomas G Bird (TG)

Cancer Research UK Beatson Institute, Glasgow, UK.
Institute of Cancer Sciences, University of Glasgow, Glasgow, UK.
MRC Centre for Inflammation Research, University of Edinburgh, Edinburgh, UK.

Dyfed Huws (D)

Welsh Cancer Intelligence and Surveillance Unit, Knowledge Directorate, Public Health Wales, Cardiff, UK.

David Wallace (D)

Department of Health Services Research and Policy, London School of Hygiene and Tropical Medicine, London, UK.

Timothy J S Cross (TJS)

Institute of Translational Medicine, The University of Liverpool, Liverpool, UK.

Ian A Rowe (IA)

Leeds Institute for Medical Research, University of Leeds, Leeds, UK.
Leeds Liver Unit, St. James's University Hospital, Leeds, UK.

Graeme Alexander (G)

UCL Institute for Liver and Digestive Health, Royal Free Hospital, London, UK.

Aileen Marshall (A)

Sheila Sherlock Liver Centre, The Royal Free Hospital, London, UK.

Classifications MeSH