TY - JOUR
T1 - Global burden of liver cancer in males and females
T2 - Changing etiological basis and the growing contribution of NASH
AU - Tan, Darren Jun Hao
AU - Setiawan, Veronica Wendy
AU - Ng, Cheng Han
AU - Lim, Wen Hui
AU - Muthiah, Mark D.
AU - Tan, Eunice X.
AU - Dan, Yock Young
AU - Roberts, Lewis R.
AU - Loomba, Rohit
AU - Huang, Daniel Q.
N1 - Funding Information:
The Agency for Science, Technology and Research (Singapore), Grant/Award Number: IAF-PP grant (H18/01/a0/017).
Funding Information:
Daniel Huang consults for Eisai. Lewis R. Roberts advises and received grants from Bayer, Exact Sciences, and Gilead Sciences. He consults for AstraZeneca, Global Science, MJH Life Sciences, Novartis Venture Fund, Pontifax, and Roche. He advises Eisai, Genentech, GRAIL, Hepion, and The Lynx Group. He received grants from Boston Scientific, Fujifilm, Glycotest, RedHill, and TARGET PharmaSolutions. Rohit Loomba consults for and received grants from AstraZeneca, Bristol‐Meyers Squibb, Eli Lilly, Galmed, Gilead, Intercept, Inventiva, Janssen, Madrigal, Merck, NGM Biopharmaceuticals, and Pfizer. He consults for Aardvark Therapeutics, Altimmune, Anylam/Regeneron, Amgen, Arrowhead Pharmaceuticals, CohBar, Glympse Bio, Hightide, Inipharm, Ionis, Metacrine, Novartis, Novo Nordisk, Sagimet, Theratechnologies, 89 Bio, and Viking Therapeutics. He received grants from Allergan, Boehringer‐Ingelheim, Galectin Therapeutics, Genfit, and Sonic Incytes. He is the co‐founder of Liponexus Inc.
Funding Information:
Supported by an IAF‐PP grant (H18/01/a0/017) from the Agency for Science, Technology and Research (Singapore) on Ensemble of Multidisciplinary Systems and Integrated Omics for NAFLD diagnostic and therapeutic discovery.
Publisher Copyright:
© 2023 John Wiley and Sons Inc.. All rights reserved.
PY - 2023/4
Y1 - 2023/4
N2 - Background and Aim: The etiology of liver diseases has changed in recent years, but its impact on the comparative burden of liver cancer between males and females is unclear. We estimated sex differences in the burden of liver cancer across 204 countries and territories from 2010 to 2019. Approach and Result: We analyzed temporal trends in the burden of liver cancer using the methodology framework of the 2019 Global Burden of Disease study. We estimated annual frequencies and age-standardized rates (ASRs) of liver cancer incidence, death, and disability-adjusted life-years (DALYs) by sex, country, region, and etiology of liver disease. Globally in 2019, the frequency of incident cases, deaths, and DALYs due to liver cancer were 376,483, 333,672, and 9,048,723 in males, versus 157,881, 150,904, and 3,479,699 in females. From 2010 to 2019, the incidence ASRs in males increased while death and DALY ASRs remained stable; incidence, death, and DALY ASRs in females decreased. Death ASRs for both sexes increased only in the Americas and remained stable or declined in remaining regions. In 2019, hepatitis B was the leading cause of liver cancer death in males, and hepatitis C in females. From 2010 to 2019, NASH had the fastest growing death ASRs in males and females. The ratio of female-to-male death ASRs in 2019 was lowest in hepatitis B (0.2) and highest in NASH (0.9). Conclusions: The overall burden of liver cancer is higher in males, although incidence and death ASRs from NASH-associated liver cancer in females approach that of males.
AB - Background and Aim: The etiology of liver diseases has changed in recent years, but its impact on the comparative burden of liver cancer between males and females is unclear. We estimated sex differences in the burden of liver cancer across 204 countries and territories from 2010 to 2019. Approach and Result: We analyzed temporal trends in the burden of liver cancer using the methodology framework of the 2019 Global Burden of Disease study. We estimated annual frequencies and age-standardized rates (ASRs) of liver cancer incidence, death, and disability-adjusted life-years (DALYs) by sex, country, region, and etiology of liver disease. Globally in 2019, the frequency of incident cases, deaths, and DALYs due to liver cancer were 376,483, 333,672, and 9,048,723 in males, versus 157,881, 150,904, and 3,479,699 in females. From 2010 to 2019, the incidence ASRs in males increased while death and DALY ASRs remained stable; incidence, death, and DALY ASRs in females decreased. Death ASRs for both sexes increased only in the Americas and remained stable or declined in remaining regions. In 2019, hepatitis B was the leading cause of liver cancer death in males, and hepatitis C in females. From 2010 to 2019, NASH had the fastest growing death ASRs in males and females. The ratio of female-to-male death ASRs in 2019 was lowest in hepatitis B (0.2) and highest in NASH (0.9). Conclusions: The overall burden of liver cancer is higher in males, although incidence and death ASRs from NASH-associated liver cancer in females approach that of males.
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U2 - 10.1002/hep.32758
DO - 10.1002/hep.32758
M3 - Article
C2 - 36037274
AN - SCOPUS:85137930751
SN - 0270-9139
VL - 77
SP - 1150
EP - 1163
JO - Hepatology
JF - Hepatology
IS - 4
ER -