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A pooled analysis of second primary pancreatic cancer

  • Min Shen
  • , Paolo Boffetta
  • , Jørgen H. Olsen
  • , Aage Andersen
  • , Kari Hemminki
  • , Eero Pukkala
  • , Elizabeth Tracey
  • , David H. Brewster
  • , Mary L. McBride
  • , Vera Pompe-Kirn
  • , Erich V. Kliewer
  • , Jon M. Tonita
  • , Kee Seng Chia
  • , Carmen Martos
  • , Jon G. Jonasson
  • , Didier Colin
  • , Ghislaine Scélo
  • , Paul Brennan
  • International Agency for Research on Cancer
  • National Institutes of Health
  • Danish Cancer Society
  • Institute of Population-Based Cancer Research
  • German Cancer Research Center
  • Karolinska Institutet
  • Finnish Cancer Registry
  • Cancer Institute NSW
  • Scottish Cancer Registry
  • Provincial Health Services Authority
  • Institute of Oncology Ljubljana
  • University of Manitoba
  • Saskatchewan Cancer Agency
  • National University of Singapore
  • Cancer Registry of Zaragoza
  • University of Iceland

Research output: Contribution to journalArticlepeer-review

32 Scopus citations

Abstract

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.

Original languageEnglish
Pages (from-to)502-511
Number of pages10
JournalAmerican Journal of Epidemiology
Volume163
Issue number6
DOIs
StatePublished - Mar 2006

Keywords

  • Neoplasms, second primary
  • Pancreatic neoplasms
  • Risk factors

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