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Original Article
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Volume 332:494-499 February 23, 1995 Number 8
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The Risk of Cancer among Patients with Cystic Fibrosis
Joseph P. Neglia, M.D., M.P.H., Stacey C. FitzSimmons, Ph.D., Patrick Maisonneuve, Martin H. Schöni, M.D., Franziska Schöni-Affolter, M.D., Mary Corey, Ph.D., Albert B. Lowenfels, M.D., for The Cystic Fibrosis and Cancer Study Group

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ABSTRACT

Background Anecdotal reports suggest an increased frequency of certain cancers in patients with cystic fibrosis, the commonest genetic disorder of whites. One third of patients with cystic fibrosis now reach adulthood, when cancer is more frequent, implying that cancer rates in these patients will increase over time. We investigated the relation between cystic fibrosis and cancer in North American and European patients with cystic fibrosis.

Methods We performed a retrospective cohort study of the occurrence of cancer in 28,511 patients with cystic fibrosis from 1985 through 1992 in the United States and Canada. The number of cases observed was compared with the number expected, calculated from population-based data on the incidence of cancer. We also analyzed proportional incidence ratios to assess the association between specific cancers and cystic fibrosis in Europe.

Results Thirty-seven cancers were observed in the North American cohort during 164,764 person-years of follow-up, as compared with an expected number of 45.6, yielding a ratio of observed to expected cancers of 0.8 (95 percent confidence interval, 0.6 to 1.1). Thirteen digestive tract tumors were observed, as compared with an expected number of two, for a ratio of observed to expected cancers of 6.5 (95 percent confidence interval, 3.5 to 11.1). In Europe, 11 of 39 cancers originated in the digestive tract, yielding a positive association between digestive tract tumors and cystic fibrosis (odds ratio, 6.4; 95 percent confidence interval, 2.9 to 14.0).

Conclusions Although the overall risk of cancer in patients with cystic fibrosis is similar to that of the general population, there is an increased risk of digestive tract cancers. Persistent or unexplained gastrointestinal symptoms in these patients should be carefully investigated.


Source Information

From the Departments of Pediatrics and Epidemiology, University of Minnesota Schools of Medicine and Public Health, Minneapolis (J.P.N.); the Cystic Fibrosis Foundation, Bethesda, Md. (S.C.F.); the Division of Epidemiology and Biostatistics, European Institute of Oncology, Milan, Italy (P.M.); Alpine Children's Hospital, Davos Platz, Switzerland (M.H.S., F.S.-A.); the Hospital for Sick Children, Toronto (M.C.); and the Departments of Surgery and Community and Preventive Medicine, New York Medical College, Valhalla (A.B.L.).

Address reprint requests to Dr. Lowenfels at the Department of Surgery, New York Medical College, Valhalla, NY 10595.

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Related Letters:

Gastrointestinal Cancer and the Cystic Fibrosis Gene
Audeh M. W., Neglia J. P., FitzSimmons S. C., Lowenfels A. B., The Cystic Fibrosis and Cancer Study Group
Extract | Full Text  
N Engl J Med 1995; 333:129-130, Jul 13, 1995. Correspondence

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