Risk of Pancreatic Cancer in the Long-Term Prospective Follow-Up of Familial Pancreatic Cancer Kindreds

Author:

Porter Nancy1ORCID,Laheru Daniel1ORCID,Lau Bryan12ORCID,He Jin3ORCID,Zheng Lei1,Narang Amol4,Roberts Nicholas J15,Canto Marcia I6ORCID,Lennon Anne Marie1345ORCID,Goggins Michael G156ORCID,Hruban Ralph H15ORCID,Klein Alison P1256ORCID

Affiliation:

1. Sidney Kimmel Comprehensive Cancer Center, Department of Oncology, Johns Hopkins School of Medicine , Baltimore, MD, USA

2. Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health , Baltimore, MD, USA

3. Department of Surgery, Johns Hopkins School of Medicine , Baltimore, MD, USA

4. Division of Radiation Oncology, Department of Medicine, Johns Hopkins School of Medicine , Baltimore, MD, USA

5. The Sol Goldman Pancreatic Cancer Research Center, Department of Pathology, Johns Hopkins University , Baltimore, MD, USA

6. Division of Gastroenterology, Department of Medicine, Johns Hopkins School of Medicine , Baltimore, MD, USA

Abstract

Abstract Background A family history of pancreatic cancer is associated with increased pancreatic cancer risk. However, risk estimates for individuals in kindreds with an aggregation of pancreatic cancer (>1 relative) are imprecise because of small samples sizes or potentially impacted by biases inherent in retrospective data. Objective The objective of this study is to determine the age-specific pancreatic cancer risk as a function of family history using prospective data. Methods We compared pancreatic cancer incidence (n = 167) in 21 141 individuals from 4433 families enrolled in the National Familial Pancreatic Cancer Registry with that expected based on Surveillance Epidemiology and End Results data and estimated the cumulative probability of pancreatic cancer using competing risk regression. Results Familial pancreatic kindred members (kindreds with pancreatic cancer in 2 first-degree relatives [FDRs] or a pathogenic variant) had a standardized incidence ratio of 4.86 (95% confidence interval [CI] = 4.01 to 5.90), and sporadic kindred members (kindreds not meeting familial criteria) had a standardized incidence ratio of 2.55 (95% CI = 1.95 to 3.34). Risk in familial pancreatic cancer kindreds increased with an increasing number of FDRs with pancreatic cancer, with a standardized incidence ratio of 3.46 (95% CI = 2.52 to 4.76), 5.44 (95% CI = 4.07 to 7.26), and 10.78 (95% CI = 6.87 to 16.89) for 1, 2, and 3 or more FDRs with pancreatic cancer, respectively. Risk was also higher among individuals with a family history of young-onset (aged younger than 50 years) pancreatic cancer. Conclusion Pancreatic cancer risk is strongly dependent on family history, including both the degree of relationship(s) and age of onset of pancreatic cancer in relatives. These risk estimates will help inform the design of early detection studies and the risk and benefit analysis of screening trials.

Funder

National Cancer Institute

Lustgarten Foundation, Rolfe Pancreatic Cancer Foundation, Dennis Troper and Susan Wojcicki

Sol Goldman Pancreatic Cancer Research Center

Publisher

Oxford University Press (OUP)

Subject

Cancer Research,Oncology

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