TY - JOUR
T1 - Aspirin and the Risk of Colorectal Cancer According to Genetic Susceptibility among Older Individuals
AU - Bakshi, Andrew
AU - Cao, Yin
AU - Orchard, Suzanne G.
AU - Carr, Prudence R.
AU - Joshi, Amit D.
AU - Manning, Alisa K.
AU - Buchanan, Daniel D.
AU - Umar, Asad
AU - Winship, Ingrid M.
AU - Gibbs, Peter
AU - Zalcberg, John R.
AU - Macrae, Finlay
AU - McNeil, John J.
AU - Lacaze, Paul
AU - Chan, Andrew T.
N1 - Publisher Copyright:
© 2022 American Association for Cancer Research Inc.. All rights reserved.
PY - 2022/7
Y1 - 2022/7
N2 - Although aspirin has been considered a promising agent for prevention of colorectal cancer, recent data suggest a lack of benefit among older individuals. Whether some individuals with higher risk of colorectal cancer may benefit from aspirin remains unknown. We used a 95-variant colorectal cancer polygenic risk score (PRS) to explore the association between genetic susceptibility to colorectal cancer and aspirin use in a prospective study of 12,609 individuals of European descent ages ≥70 years, enrolled in the ASPirin in Reducing Events in the Elderly (ASPREE) double-blinded, placebo-controlled randomized trial (randomized controlled trial; RCT). Cox proportional hazards models were used to assess the association of aspirin use on colorectal cancer, as well as the interaction between the PRS and aspirin treatment on colorectal cancer. Over a median of 4.7 years follow-up, 143 participants were diagnosed with incident colorectal cancer. Aspirin assignment was not associated with incidence of colorectal cancer overall [HR = 0.94; 95% confidence interval (CI), 0.68-1.30] or within strata of PRS (P for interaction = 0.97). However, the PRS was associated with an increased risk of colorectal cancer (HR = 1.28 per SD; 95% CI, 1.09-1.51). Individuals in the top quintile of the PRS distribution had an 85% higher risk compared with individuals in the bottom quintile (HR=1.85; 95%CI, 1.08-3.15). In a prospective RCT of older individuals, aPRS is associatedwith incident colorectal cancer risk, but aspirin usewas not associatedwith a reduction of incident colorectal cancer, regardless of baseline genetic risk.
AB - Although aspirin has been considered a promising agent for prevention of colorectal cancer, recent data suggest a lack of benefit among older individuals. Whether some individuals with higher risk of colorectal cancer may benefit from aspirin remains unknown. We used a 95-variant colorectal cancer polygenic risk score (PRS) to explore the association between genetic susceptibility to colorectal cancer and aspirin use in a prospective study of 12,609 individuals of European descent ages ≥70 years, enrolled in the ASPirin in Reducing Events in the Elderly (ASPREE) double-blinded, placebo-controlled randomized trial (randomized controlled trial; RCT). Cox proportional hazards models were used to assess the association of aspirin use on colorectal cancer, as well as the interaction between the PRS and aspirin treatment on colorectal cancer. Over a median of 4.7 years follow-up, 143 participants were diagnosed with incident colorectal cancer. Aspirin assignment was not associated with incidence of colorectal cancer overall [HR = 0.94; 95% confidence interval (CI), 0.68-1.30] or within strata of PRS (P for interaction = 0.97). However, the PRS was associated with an increased risk of colorectal cancer (HR = 1.28 per SD; 95% CI, 1.09-1.51). Individuals in the top quintile of the PRS distribution had an 85% higher risk compared with individuals in the bottom quintile (HR=1.85; 95%CI, 1.08-3.15). In a prospective RCT of older individuals, aPRS is associatedwith incident colorectal cancer risk, but aspirin usewas not associatedwith a reduction of incident colorectal cancer, regardless of baseline genetic risk.
UR - http://www.scopus.com/inward/record.url?scp=85134083408&partnerID=8YFLogxK
U2 - 10.1158/1940-6207.CAPR-22-0011
DO - 10.1158/1940-6207.CAPR-22-0011
M3 - Article
C2 - 35348611
AN - SCOPUS:85134083408
SN - 1940-6207
VL - 15
SP - 447
EP - 454
JO - Cancer Prevention Research
JF - Cancer Prevention Research
IS - 7
ER -