A pooled analysis of second primary pancreatic cancer

被引:29
作者
Shen, M
Boffetta, P
Olsen, JH
Andersen, A
Hemminki, K
Pukkala, E
Tracey, E
Brewster, DH
McBride, ML
Pompe-Kirn, V
Kliewer, EV
Tonita, JM
Chia, KS
Martos, C
Jonasson, JG
Colin, D
Scélo, G
Brennan, P
机构
[1] NCI, Occupat & Environm Epidemiol Branch, Div Canc Epidemiol & Genet, NIH,Dept Hlth & Human Serv, Bethesda, MD 20892 USA
[2] Int Agcy Res Canc, F-69372 Lyon, France
[3] Danish Canc Soc, Inst Canc Epidemiol, Copenhagen, Denmark
[4] Inst Populat Based Canc Res, Oslo, Norway
[5] German Canc Res Ctr, Div Mol Genet Epidemiol, D-6900 Heidelberg, Germany
[6] Karolinska Inst, Novum, Dept Biosci, Huddinge, Sweden
[7] Finnish Canc Registry, Inst Stat & Epidemiol Canc Res, FIN-00170 Helsinki, Finland
[8] New S Wales Cent Canc Registry, Inst Canc, Eveleigh, NSW, Australia
[9] Scottish Canc Registry, Informat Serv, Natl Hlth Serv, Edinburgh, Midlothian, Scotland
[10] British Columbia Canc Agcy, Vancouver, BC V5Z 4E6, Canada
[11] Can Registry Slovenia, Inst Oncol, Ljubljana, Slovenia
[12] CancerCare Manitoba, Epidemiol & Canc Registry, Winnipeg, MB, Canada
[13] Univ Manitoba, Winnipeg, MB, Canada
[14] Saskatchewan Canc Agcy, Regina, SK, Canada
[15] Natl Univ Singapore, Ctr Mol Epidemiol, Singapore 117548, Singapore
[16] Singapore Canc Registry, Singapore, Singapore
[17] Canc Registry Zaragoza, Hlth Dept Aragon Govt, Zaragoza, Spain
[18] Univ Iceland, Fac Med, Reykjavik, Iceland
[19] Iceland Canc Soc, Iceland Canc Registry, Reykjavik, Iceland
关键词
neoplasms; second primary; pancreatic neoplasms; risk factors;
D O I
10.1093/aje/kwj073
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Studies of pancreatic cancer in the setting of second primary malignant neoplasms can provide etiologic clues. An international multicenter study was carried out using data from 13 cancer registries with a registration period up to year 2000. Cancer patients were followed up from the initial cancer diagnosis, and the occurrence of second primary malignant neoplasms was compared with expected values derived from local rates, adjusting for age, sex, and period of diagnosis. Results from individual registries were pooled by use of a fixed-effects model. People were at higher risk of developing pancreatic cancer within 10 years of a diagnosis of cancers of the pharynx, stomach, gallbladder, larynx, lung, cervix, corpus uteri, bladder, and eye and 10 years or later following a diagnosis of cancers of the stomach, colon, gallbladder, breast, cervix, placenta, corpus uteri, ovary, testis, bladder, kidney, and eye, as well as Hodgkin's and non-Hodgkin's lymphomas. Pancreatic cancer was connected with smoking-related cancers, confirming the etiologic role of tobacco. The associations with uterine and ovarian cancers suggest that reproductive factors might be implicated in pancreatic carcinogenesis. The elevated pancreatic cancer risk in young patients observed among several types of cancer implies a role of genetic factors. Radiotherapy is also suggested as a risk factor.
引用
收藏
页码:502 / 511
页数:10
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