Epidemiology of gastrointestinal cancers: a systematic analysis from the Global Burden of Disease Study 2021.

ALCOHOLIC LIVER DISEASE CANCER COLORECTAL CANCER EPIDEMIOLOGY NONALCOHOLIC STEATOHEPATITIS

Journal

Gut
ISSN: 1468-3288
Titre abrégé: Gut
Pays: England
ID NLM: 2985108R

Informations de publication

Date de publication:
06 Sep 2024
Historique:
received: 27 06 2024
accepted: 21 08 2024
medline: 7 9 2024
pubmed: 7 9 2024
entrez: 6 9 2024
Statut: aheadofprint

Résumé

Gastrointestinal cancers comprise nearly one-third of global mortality from cancer, yet the comprehensive global burden of these cancers remains uninvestigated. We aimed to assess the global, regional and national burden of gastrointestinal cancers. Data on oesophagus, gastric, colorectal, liver, pancreas and biliary tract cancers were extracted from the Global Burden of Disease 2021 database. Age-standardised incidence rate (ASIR) and age-standardised death rate (ASDR) were calculated by sex, region and Sociodemographic Index (SDI). In 2021, there were 5.26 million incidences and 3.70 million deaths from gastrointestinal cancer. The greatest burden is from colorectal, followed by gastric, oesophageal, pancreatic, liver and biliary tract cancer. We noted geographical and socioeconomic differences in ASIR and ASDR across all types of cancers. From 2000 to 2021, ASIR increased for colorectal cancer (annual percent change (APC): 0.10%, 95% CI 0.05% to 0.14%), pancreatic cancer (APC: 0.27%, 95% CI 0.14% to 0.41%), and liver cancer from metabolic dysfunction-associated steatotic liver disease (APC: 0.62%, 95% CI 0.58% to 0.67%) and alcohol-related liver disease (APC: 0.26%, 95% CI 0.22% to 0.30%). ASDR increased for pancreatic cancer (APC: 0.18%, 95% CI 0.02% to 0.34%). Higher SDI countries had higher incidence rates for most types of gastrointestinal cancer. Although the ASIR of oesophageal, gastric and biliary tract cancer has decreased, the ASIR still increased in colorectal, pancreatic and liver cancer from steatotic liver disease. Public policies are important for controlling gastrointestinal cancers-most importantly, reducing alcohol consumption, hepatitis B immunisation and tackling the burden of metabolic diseases.

Sections du résumé

BACKGROUND BACKGROUND
Gastrointestinal cancers comprise nearly one-third of global mortality from cancer, yet the comprehensive global burden of these cancers remains uninvestigated.
OBJECTIVE OBJECTIVE
We aimed to assess the global, regional and national burden of gastrointestinal cancers.
DESIGNS METHODS
Data on oesophagus, gastric, colorectal, liver, pancreas and biliary tract cancers were extracted from the Global Burden of Disease 2021 database. Age-standardised incidence rate (ASIR) and age-standardised death rate (ASDR) were calculated by sex, region and Sociodemographic Index (SDI).
RESULTS RESULTS
In 2021, there were 5.26 million incidences and 3.70 million deaths from gastrointestinal cancer. The greatest burden is from colorectal, followed by gastric, oesophageal, pancreatic, liver and biliary tract cancer. We noted geographical and socioeconomic differences in ASIR and ASDR across all types of cancers. From 2000 to 2021, ASIR increased for colorectal cancer (annual percent change (APC): 0.10%, 95% CI 0.05% to 0.14%), pancreatic cancer (APC: 0.27%, 95% CI 0.14% to 0.41%), and liver cancer from metabolic dysfunction-associated steatotic liver disease (APC: 0.62%, 95% CI 0.58% to 0.67%) and alcohol-related liver disease (APC: 0.26%, 95% CI 0.22% to 0.30%). ASDR increased for pancreatic cancer (APC: 0.18%, 95% CI 0.02% to 0.34%). Higher SDI countries had higher incidence rates for most types of gastrointestinal cancer.
CONCLUSIONS CONCLUSIONS
Although the ASIR of oesophageal, gastric and biliary tract cancer has decreased, the ASIR still increased in colorectal, pancreatic and liver cancer from steatotic liver disease. Public policies are important for controlling gastrointestinal cancers-most importantly, reducing alcohol consumption, hepatitis B immunisation and tackling the burden of metabolic diseases.

Identifiants

pubmed: 39242191
pii: gutjnl-2024-333227
doi: 10.1136/gutjnl-2024-333227
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© Author(s) (or their employer(s)) 2024. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: MBW declared the conflict of interest as designated below: Consulting: Cosmo/Aries Pharmaceuticals, Verily, Boston Scientific, Endiatix, Intervenn, AlphaMed UAE, Fujifilm. Research grants: Fujifilm, Boston Scientific, Olympus, Medtronic, Ninepoint Medical, Cosmo/Aries Pharmaceuticals. Stock/Stock Options: Virgo Inc. Consulting on behalf of Mayo Clinic: Boston Scientific, Microtek. General payments/Minor Food and Beverage: Boston Scientific and Cook Medical. All other coauthors denied conflict of interest. LRR has been on advisory boards for AstraZeneca, Bayer, Eisai, Exact Sciences, Focus Medical Communication, Gilead Sciences, GRAIL, Inc., Novartis Venture Fund, Pontifax, and Roche. LR has received research support from Bayer, Boston Scientific, Exact Sciences, Fujifilm Medical Systems, Genentech, Gilead Sciences, Glycotest, Inc., HERMES, Innovo Bioanalysis, RedHill Biopharma, and TARGET Real World Evidence.

Auteurs

Pojsakorn Danpanichkul (P)

Department of Internal Medicine, Texas Tech University Health Sciences Center, Lubbock, Texas, USA pojsakorndan@gmail.com dr.karn.wi@gmail.com.

Kanokphong Suparan (K)

Department of Microbiology, Chiang Mai University, Chiang Mai, Thailand.

Primrose Tothanarungroj (P)

Faculty of Medicine, Chiang Mai University, Chiang Mai, Thailand.

Disatorn Dejvajara (D)

Faculty of Medicine, Chiang Mai University, Chiang Mai, Thailand.

Krittameth Rakwong (K)

Faculty of Medicine, Chiang Mai University, Chiang Mai, Thailand.

Yanfang Pang (Y)

Department of Microbiology, Chiang Mai University, Chiang Mai, Thailand.
Affiliated Hospital of Youjiang Medical University of Nationalities, Baise, Guangxi, People's Republic of China.
National Immunological Laboratory for Traditional Chinese Medicine, Baise, Guangxi, People's Republic of China.
Key Laboratory of Research on Clinical Molecular Diagnosis for High Incidence Diseases in Western Guangxi, Guangxi, Guangxi, People's Republic of China.

Romelia Barba (R)

Department of Internal Medicine, Texas Tech University Health Sciences Center, Lubbock, Texas, USA.

Jerapas Thongpiya (J)

Department of Internal Medicine, Texas Tech University Health Sciences Center, Lubbock, Texas, USA.

Michael B Fallon (MB)

Division of Gastroenterology and Hepatology, Department of Medicine, The University of Arizona College of Medicine Phoenix, Phoenix, Arizona, USA.
Division of Gastroenterology and Hepatology, Department of Internal Medicine, Banner - University Medical Center Phoenix, Phoenix, Arizona, USA.

Denise Harnois (D)

Division of Gastroenterology and Hepatology, Mayo Clinic, Jacksonville, Florida, USA.

Rashid N Lui (RN)

Institute of Digestive Disease, Chinese University of Hong Kong, New Territories, Hong Kong, People's Republic of China.

Michael B Wallace (MB)

Division of Gastroenterology and Hepatology, Mayo Clinic, Jacksonville, Florida, USA.

Ju Dong Yang (JD)

Karsh Division of Gastroenterology and Hepatology, Comprehensive Transplant Center, and Samuel Oschin Comprehensive Cancer Institute, Cedars-Sinai Medical Center, Los Angeles, California, USA.

Lewis R Roberts (LR)

Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota, USA.

Karn Wijarnpreecha (K)

Division of Gastroenterology and Hepatology, Department of Medicine, The University of Arizona College of Medicine Phoenix, Phoenix, Arizona, USA pojsakorndan@gmail.com dr.karn.wi@gmail.com.
Division of Gastroenterology and Hepatology, Department of Internal Medicine, Banner - University Medical Center Phoenix, Phoenix, Arizona, USA.
Mayo Clinic Florida, Jacksonville, Florida, USA.

Classifications MeSH