The age-dependent association of risk factors with pancreatic cancer

被引:24
|
作者
Yuan, C. [1 ,2 ]
Kim, J. [3 ]
Wang, Q. L. [1 ,2 ]
Lee, A. A. [2 ,4 ]
Babic, A. [1 ,2 ]
Amundadottir, L. T. [5 ]
Klein, A. P. [6 ,7 ]
Li, D. [8 ]
McCullough, M. L. [9 ]
Petersen, G. M. [10 ]
Risch, H. A. [11 ]
Stolzenberg-Solomon, R. Z. [5 ]
Perez, K. [1 ,2 ]
Ng, K. [1 ,2 ]
Giovannucci, E. L. [3 ,12 ,13 ]
Stampfer, M. J. [3 ,12 ,13 ]
Kraft, P. [3 ,14 ]
Wolpin, B. M. [1 ,2 ]
机构
[1] Dana Farber Canc Inst, Dept Med Oncol, Boston, MA 02215 USA
[2] Harvard Med Sch, Boston, MA 02115 USA
[3] Harvard TH Chan Sch Publ Hlth, Dept Epidemiol, Boston, MA USA
[4] Brigham & Womens Hosp, Div Gastroenterol Hepatol & Endoscopy, 75 Francis St, Boston, MA 02115 USA
[5] NCI, Div Canc Epidemiol & Genet, Rockville, MD USA
[6] Johns Hopkins Sch Med, Sidney Kimmel Comprehens Canc Ctr, Dept Oncol, Baltimore, MD USA
[7] Johns Hopkins Sch Med, Sol Goldman Pancreat Canc Res Ctr, Dept Pathol, Baltimore, MD USA
[8] Univ Texas MD Anderson Canc Ctr, Dept Gastrointestinal Med Oncol, Houston, TX 77030 USA
[9] Amer Canc Soc, Dept Populat Sci, Atlanta, GA 30329 USA
[10] Mayo Clin, Coll Med, Dept Quantitat Hlth Sci, Rochester, MN USA
[11] Yale Sch Publ Hlth, Dept Chron Dis Epidemiol, New Haven, CT USA
[12] Harvard TH Chan Sch Publ Hlth, Dept Nutr, Boston, MA USA
[13] Brigham & Womens Hosp, Channing Div Network Med, 75 Francis St, Boston, MA 02115 USA
[14] Harvard TH Chan Sch Publ Hlth, Dept Biostat, Boston, MA USA
基金
美国国家卫生研究院;
关键词
pancreatic cancer; age; risk factor; lifestyle modification; polygenic risk score; GENOME-WIDE ASSOCIATION; SUSCEPTIBILITY LOCI; OF-ONSET; ALCOHOL-CONSUMPTION; INDEX; METAANALYSIS; PREVALENCE; MUTATIONS; SMOKING; OBESITY;
D O I
10.1016/j.annonc.2022.03.276
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Pancreatic cancer presents as advanced disease in >80% of patients; yet, appropriate ages to consider prevention and early detection strategies are poorly defined. We investigated age-specific associations and attributable risks of pancreatic cancer for established modifiable and non-modifiable risk factors. Patients and methods: We included 167 483 participants from two prospective US cohort studies with 1190 incident cases of pancreatic cancer during >30 years of follow-up; 5107 pancreatic cancer cases and 8845 control participants of European ancestry from a completed multicenter genome-wide association study (GWAS); and 248 893 pancreatic cancer cases documented in the US Surveillance, Epidemiology, and End Results (SEER) Program. Across different age categories, we investigated cigarette smoking, obesity, diabetes, height, and non-O blood group in the prospective cohorts; weighted polygenic risk score of 22 previously identified single nucleotide polymorphisms in the GWAS; and male sex and black race in the SEER Program. Results: In the prospective cohorts, all five risk factors were more strongly associated with pancreatic cancer risk among younger participants, with associations attenuated among those aged> 70 years. The hazard ratios comparing participants with three to five risk factors with those with no risk factors were 9.24 [95% confidence interval (CI) 4.11-20.77] among those aged <= 60 years, 3.00 (95% CI 1.85-4.86) among those aged 61-70 years, and 1.46 (95% CI 1.10-1.94) among those aged >70 years (P-heterogeneity = 3x10(-5)). These factors together were related to 65.6%, 49.7%, and 17.2% of incident pancreatic cancers in these age groups, respectively. In the GWAS and the SEER Program, the associations with the polygenic risk score, male sex, and black race were all stronger among younger individuals (P-heterogeneity <= 0.01). Conclusions: Established risk factors are more strongly associated with earlier-onset pancreatic cancer, emphasizing the importance of age at initiation for cancer prevention and control programs targeting this highly lethal malignancy.
引用
收藏
页码:693 / 701
页数:9
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