Risk of pancreatic cancer in cystic fibrosis and cystic fibrosis transmembrane conductance regulator (CFTR) germline variants: A retrospective cohort study.

Abstract

Purpose: Screening guidelines for pancreatic cancer (PC) based on genetic risk do not include patients with CF or CFTR gene variants. The objective of this study was to determine risk of PC in patients with CF or CFTR pathogenic/likely pathogenic (PLPV) gene variants.

Methods: We conducted a retrospective cohort study of CF/CFTR PLPV patients in an integrated healthcare system from 2008-2023. Index date was the initial encounter within the health system, with censoring at loss of membership, death, or study completion. PC incidence rate (IR) was based on person-time at risk. Age- and sex-adjusted standardized incidence rate ratio (SIR) for PC was calculated for CF/CFTR compared to the non-CFTR reference population. We further stratified PC risk by age and family history of PC.

Results: 12,682 patients with CF/CFTR were included with a median follow-up of 8.3 years (IQR 4.3-13.1). The cohort was 88% female, had median age at index of 25.8 (IQR 19.1-31.1) years, and was majority White and Hispanic. 8 total PC events occurred in the CF/CFTR group (IR 7.3 per 100,000 person-years). The adjusted SIR for PC was 2.3 (95% CL 1.2-4.7) for CF/CFTR variant patients. There was effect modification by age, with SIR (age≥50 years) of 2.87 (95% CL 1.37-6.01). Among CF/CFTR patients with family history of PC, 1 PC case was observed with SIR (age≥50 years) of 13.

Conclusion: Patients with CF or CFTR gene variants had an almost 3-fold higher adjusted risk of PC than the general population after age 50 years. The risk may be further increased with a family history of PC.