Type 2 diabetes and the risk of gastrointestinal cancers in individuals with metabolic dysfunction associated steatotic liver disease.
Abstract
493 Background: Metabolic dysfunction-associated steatotic liver disease (MASLD), accompanied by type 2 diabetes mellitus, is linked to an increased risk of liver and cardiovascular complications compared to MASLD without diabetes; however, the association with gastrointestinal cancer risk remains largely understudied. Methods: We conducted a population-based retrospective cohort study using the TriNetX platform, which aggregates de-identified electronic health records from healthcare organizations across the United States. Individuals with MASLD were stratified based on the presence or absence of type 2 diabetes mellitus. The primary outcomes included gastrointestinal cancers and their subtypes, assessed over a 5-year follow-up period using Cox proportional hazards regression models. Results: Among matched MASLD patients, those with T2DM had a higher 5-year incidence of all GI cancers (1.6% vs. 0.8%; HR 1.71, 95% CI: 1.56–1.88). The increased risk was most pronounced for liver cancer (0.6% vs. 0.2%; HR 2.32, 95% CI: 1.94–2.76), pancreatic cancer (0.4% vs. 0.2%; HR 1.86, 95% CI: 1.51–2.28), and intrahepatic bile duct cancer (0.1% vs. 0.0%; HR 1.92, 95% CI: 1.31–2.80). No statistically significant differences were observed for other GI cancer subtypes. Conclusions: T2DM was independently associated with a significantly increased risk of several GI cancers among MASLD patients, especially liver, pancreatic, and intrahepatic bile duct cancers. These findings support enhanced cancer surveillance in this high-risk group. 5-year incidence of clinical outcome with type 2 diabetes and without type 2 diabetes in individuals with metabolic dysfunction-associated steatotic liver disease. Outcome MASLD with T2DM Events N (%) MASLD without T2DM Events N (%) Hazard Ratio (95% CI) p-value Gastrointestinal cancer 1,354 (1.6%) 650 (0.8%) 1.71 (1.56−1.88) <0.001 Esophageal cancer 52 (0.1%) 38 (0.0%) 1.12 (0.74−1.71) 0.59 Gastric cancer 98 (0.1%) 74 (0.1%) 1.10 (0.81−1.48) 0.556 Liver cancer 468 (0.6%) 167 (0.2%) 2.32 (1.94−2.76) <0.001 Colorectal cancer 135 (0.2%) 99 (0.1%) 1.13 (0.87−1.47) 0.354 Pancreatic cancer 298 (0.4%) 133 (0.2%) 1.86 (1.51−2.28) <0.001 Intrahepatic bile duct cancer 89 (0.1%) 38 (0.0%) 1.92 (1.31−2.80) 0.001 Extrahepatic bile duct cancer 30 (0.0%) 23 (0.0%) 1.07 (0.62−1.84) 0.809 Gallbladder cancer 16 (0.0%) 16 (0.0%) 0.82 (0.41−1.65) 0.582 Small intestinal cancer 54 (0.1%) 49 (0.1%) 0.91 (0.62−1.35) 0.647 Anal cancer 46 (0.1%) 34 (0.0%) 1.11 (0.71−1.73) 0.636 Ill-defined GI cancer 41 (0.0%) 24 (0.0%) 1.40 (0.85−2.32) 0.185 CI: confidence interval; HR: Hazard Ratio.
Article Details
Journal Info
Journal of Clinical Oncology
Lippincott Williams & Wilkins
Authors (8)
Pojsakorn Danpanichkul
Texas Tech University, Lubbock, Texas, United States
Shu-Yen Chan
Department of Internal Medicine, Weiss Memorial Hospital, Chicago, IL
Natchaya Polpichai
Department of Medicine, Weiss Memorial Hospital, Chicago, IL
Rinrada Worapongpaiboon
National Institutes of Health, Maryland, MD
Sakditad Saowapa
Texas Tech Health Sciences Center, Lubbock, Texas, United States
Omar Al Ta'ani
University of Pittsburgh Medical Center (UPMC), Pittsburgh, PA
Chalothorn Wannaphut
1MD Anderson Cancer Center, Houston, United States
Abdelrahman Attia
Cedars-Sinai Medical Center, Los Angeles, CA