Background Surveillance for pancreatic ductal adenocarcinoma (PDAC) is recommended for high-risk individuals with genetic variants in PDAC-associated genes and/or family history. Surveillance uptake and adherence may depend on the perception of PDAC risk and cancer worry. We aimed to determine PDAC risk perception in at-risk individuals and assess factors associated with PDAC surveillance uptake.
Methods At-risk individuals identified from a prospective academic registry were sent a survey electronically. PDAC risk perception, cancer worry and surveillance uptake were surveyed. Factors associated with increased risk perception and surveillance were assessed. Five-year PDAC risk was calculated using the PancPRO risk assessment model, and correlation with subjective risk assessment was assessed.
Results The overall survey response rate was 34% (279/816). The median perceived PDAC risk was twofold (IQR 1–4) above respondents’ estimates of general population risk. Factors significantly associated with higher perceived PDAC risk included non-Hispanic white race, post-graduate education level, PDAC-affected first-degree relative, genetic variants and lack of personal cancer history. Cancer worry had a very weak correlation across PDAC risk estimates (r=0.16). No correlation between perceived PDAC risk and 5-year calculated PDAC risk was found. Older age, having a first-degree relative with PDAC, meeting with a medical provider about PDAC cancer risk and awareness of surveillance modalities were significant predictors of undergoing PDAC surveillance.
Conclusions Individuals at risk for PDAC do not report risk perception that correlates with calculated risk. This presents an opportunity for counselling of at-risk patients to individualise management and improve surveillance uptake for eligible individuals.
- pancreatic diseases
- population characteristics
Data availability statement
Data are available upon reasonable request.
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DN and OG contributed equally.
Presented at Portions of this manuscript were presented at Digestive Disease Week 2022, San Diego, California, 21–24 May 2022.
Contributors DN and OG: formal analysis; writing—original draft, review and editing. CMD: conceptualisation; resources; writing—review and editing. ZE: resources and data curation; writing—review and editing. CL: formal analysis; writing—review and editing. SSK: conceptualisation; writing—review and editing; supervision. Guarantor of the study: SSK.
Funding The authors have not declared a specific grant for this research from any funding agency in the public, commercial or not-for-profit sectors.
Competing interests None declared.
Provenance and peer review Not commissioned; externally peer reviewed.
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