TY - JOUR
T1 - Risk of Pancreatic Cancer in the Long-Term Prospective Follow-Up of Familial Pancreatic Cancer Kindreds
AU - Porter, Nancy
AU - Laheru, Daniel
AU - Lau, Bryan
AU - He, Jin
AU - Zheng, Lei
AU - Narang, Amol
AU - Roberts, Nicholas J.
AU - Canto, Marcia I.
AU - Lennon, Anne Marie
AU - Goggins, Michael G.
AU - Hruban, Ralph H.
AU - Klein, Alison P.
N1 - Publisher Copyright:
© 2022 The Author(s). Published by Oxford University Press. All rights reserved.
PY - 2022/12/1
Y1 - 2022/12/1
N2 - 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 21141 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.
AB - 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 21141 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.
UR - https://www.scopus.com/pages/publications/85144094102
UR - https://www.scopus.com/pages/publications/85144094102#tab=citedBy
U2 - 10.1093/jnci/djac167
DO - 10.1093/jnci/djac167
M3 - Article
C2 - 36029239
AN - SCOPUS:85144094102
SN - 0027-8874
VL - 114
SP - 1681
EP - 1688
JO - Journal of the National Cancer Institute
JF - Journal of the National Cancer Institute
IS - 12
ER -