Abstract 1356P
Background
Cancer is the second leading cause of death. Social vulnerabilities are known to be associated with worse health outcomes. However, the association of cancer mortality with underlying SEV is unexplored.
Methods
Percentile ranking scores (PRS) were calculated for each US county using social vulnerability indices from agency for toxic substances and disease registry (ATSDR). PRS (ranging from 0-1) were then categorized into quartiles (Q: 1st: 0-0.25 [least vulnerable]; 4th:0.75-1.00 [most vulnerable]). County level age adjusted mortality rates (AAMR) per 100,000 person-years (PY) were extracted for leading causes of cancer deaths (lung/bronchus, colon/rectal, hepatobiliary, pancreas, breast, ovary, and prostate) from wide ranging online data for epidemiological research (WONDER) database and were linked with quartile rankings. Rate ratios (RR) of AAMRs between 4th and 1st Q were then estimated with 95% confidence intervals using population weighted, poission regression.
Results
Data from 3060 US counties were included in this analysis. The overall cancer related AAMR per 100,000 PY was 128.9. A stepwise increase was observed in AAMRs from the 1st to 4th Q (114.5 vs 141.5) for overall cancers. AAMRs were significantly higher in counties in 4th Q for hepatobiliary, (RR: 1.52, [95% CI: 1.45-1.61]), colorectal (1.21 [1.16-1.26]), breast (1.11 [1.07-1.15]) and prostate cancers (1.19 [1.14-1.24]) as compared to AAMRs in the 1st Q. No significant differences were observed for other cancers. Significantly higher AAMRs were observed in 4th Q as compared to 1st Q in patients <65 years (premature mortality) for all cancers (1.31 [1.20-1.42]). AAMRs of Hispanic patients with lung (1.31 [1.14-1.51]), colorectal (1.48 [1.28-1.72]), pancreatic (1.25 [1.10-1.43]), and hepatobiliary cancers (1.44 [1.20-1.73]) were significantly higher in 4th Q compared to 1st Q. Similar results were observed for non-Hispanic Black patients with lung, colorectal and hepatobiliary cancer.
Conclusions
There may be an increased risk of premature cancer mortality in socioeconomically vulnerable US counties. Similar investigations should be done globally to understand the impact of SEV on cancer mortality across different regions of the world.
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
Syed Arsalan Ahmed Naqvi.
Funding
Has not received any funding.
Disclosure
All authors have declared no conflicts of interest.