Temporal trends in metabolic syndrome–associated mortality among patients with upper gastrointestinal cancers, 1999–2020: A CDC WONDER analysis.

Z Zoha Kashif (University College of Medicine and Dentistry, Lahore, Pakistan) S Suleman Saeed (7University College of Medicine and Dentistry, Lahore, Pakistan) H Hamid Bin Tariq (University College of Medicine and Dentistry, Lahore, Pakistan) H Humza Aftab (University College of Medicine and Dentistry, Lahore, Pakistan) A Aiman Aijaz (University College of Medicine and Dentistry, Lahore, Pakistan) A Abdullah Abbas I Izza Zahra (5Foundation University Medical College, Islamabad, Pakistan) M Mehmood Hassan (Ameer-ud-Din Medical College, Lahore, Pakistan) I Ibraheem Muhemmed Mustafa (King Edward Medical University, Lahore, Pakistan) I Izma Kashif (University College of Medicine and Dentistry, Lahore, Pakistan) B Bilal Ahmad R Rana Uzair Ahmad (8Trinity Health Livonia, Michigan, Livonia, United States) M Mahnoor Jan (Shaikh Khalifa Bin Zayed Al-Nahyan Medical and Dental College, Lahore, Pakistan)

Abstract

e16062 Background: Upper gastrointestinal (UGI) cancers remain a major cause of cancer mortality in the United States. Metabolic disorders, including diabetes, obesity, dyslipidemia, and hypertension, may worsen prognosis and contribute to disparities in outcomes. However, national mortality trends assessing UGI cancer deaths in the context of metabolic comorbidities are not wellcharacterized. Methods: A retrospective population-based analysis was conducted using the CDC WONDER Multiple Cause of Death database (1999–2020). Deaths with oesophageal or gastric cancer as the underlying cause and metabolic disorders as contributing causes were included. Age-adjusted mortality rates (AAMRs) per 100,000 population and annual percent change (APC) were calculated. Joinpoint regression was done and analyses were stratified by age, sex, race/ethnicity, urbanisation, and state. Results: From 1999 to 2020, 45,086 deaths occurred among adults with UGI cancers and metabolic comorbidities. Overall AAMRs increased from 2.0 to 4.2 per 100,000, with a significant rise from 1999 to 2009 (APC 4.30%; 95% CI, 2.97–5.56; p < 0.01), a modest decline from 2009 to 2014 (APC −3.50%; 95% CI, −7.45 to 0.61; p = 0.08), and a sharp increase from 2014 to 2020 (APC 6.44%; 95% CI, 4.35–8.57; p < 0.01). Age-stratified analysis demonstrated the highest crude mortality among adults aged ≥85 years (5.2 to 9.3; APC 0.55%; 95% CI, 0.03–1.08; p = 0.03) and the lowest among those aged 45–54 years (0.1 to 0.3; APC 3.53%; 95% CI, 2.06–5.02; p < 0.01). Males consistently exhibited higher mortality than females (overall AAMR 1.7 vs. 1.0), with significant increases among males from 1999–2006 (APC 5.95%; 95% CI, 3.60–8.35; p < 0.01) and 2017–2020 (APC 7.46%; 95% CI, 2.19–13.00; p < 0.01). Racial disparities were observed, with the highest AAMR among Non-Hispanic (NH) Black individuals (3.0), followed by Hispanics (2.2; APC 1.36%; 95% CI, 0.71–2.01; p < 0.01), NH Asian or Pacific Islanders (2.0; APC −0.47%; 95% CI, −1.39 to 0.45; p = 0.29), and NH Whites (1.6; APC 5.43%; 95% CI, 3.11–7.81; p < 0.01). By urbanisation, micropolitan areas demonstrated the highest AAMR (2.0; APC 2.46%; 95% CI, 1.81–3.11; p < 0.01), followed by large metropolitan and non-core areas (1.9 each), while large fringe metropolitan areas had the lowest AAMR (1.5). The District of Columbia (2.7), Mississippi (2.6), California (2.5), Hawaii (2.5), Nebraska (2.5), and Ohio (2.5) had state-level AAMRs above the 90th percentile (≥2.49 per 100,000). Conclusions: UGI cancer mortality associated with metabolic comorbidities increased substantially from 1999 to 2020, with pronounced disparities by age, sex, race, urbanization, and state. These findings underscore the need for targeted prevention strategies addressing metabolic health and geographic inequities to reduce UGI cancer mortality.

Article Details

Volume / Issue Vol. 44, Issue 16_suppl
Published June 01, 2026
ISSN 0732-183X
Publisher Lippincott Williams & Wilkins

Journal Info

Journal of Clinical Oncology

Lippincott Williams & Wilkins

ISSN: 0732-183X Health Sciences

Authors (13)

Z

Zoha Kashif

University College of Medicine and Dentistry, Lahore, Pakistan

S

Suleman Saeed

7University College of Medicine and Dentistry, Lahore, Pakistan

H

Hamid Bin Tariq

University College of Medicine and Dentistry, Lahore, Pakistan

H

Humza Aftab

University College of Medicine and Dentistry, Lahore, Pakistan

A

Aiman Aijaz

University College of Medicine and Dentistry, Lahore, Pakistan

A

Abdullah Abbas

I

Izza Zahra

5Foundation University Medical College, Islamabad, Pakistan

M

Mehmood Hassan

Ameer-ud-Din Medical College, Lahore, Pakistan

I

Ibraheem Muhemmed Mustafa

King Edward Medical University, Lahore, Pakistan

I

Izma Kashif

University College of Medicine and Dentistry, Lahore, Pakistan

B

Bilal Ahmad

R

Rana Uzair Ahmad

8Trinity Health Livonia, Michigan, Livonia, United States

M

Mahnoor Jan

Shaikh Khalifa Bin Zayed Al-Nahyan Medical and Dental College, Lahore, Pakistan