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
Background Anecdotal reports suggest an increased frequencyof certain cancers in patients with cystic fibrosis, the commonestgenetic disorder of whites. One third of patients with cysticfibrosis now reach adulthood, when cancer is more frequent,implying that cancer rates in these patients will increase overtime. We investigated the relation between cystic fibrosis andcancer in North American and European patients with cystic fibrosis.
Methods We performed a retrospective cohort study of the occurrenceof cancer in 28,511 patients with cystic fibrosis from 1985through 1992 in the United States and Canada. The number ofcases observed was compared with the number expected, calculatedfrom population-based data on the incidence of cancer. We alsoanalyzed proportional incidence ratios to assess the associationbetween specific cancers and cystic fibrosis in Europe.
Results Thirty-seven cancers were observed in the North Americancohort during 164,764 person-years of follow-up, as comparedwith an expected number of 45.6, yielding a ratio of observedto 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 observedto expected cancers of 6.5 (95 percent confidence interval,3.5 to 11.1). In Europe, 11 of 39 cancers originated in thedigestive tract, yielding a positive association between digestivetract tumors and cystic fibrosis (odds ratio, 6.4; 95 percentconfidence interval, 2.9 to 14.0).
Conclusions Although the overall risk of cancer in patientswith cystic fibrosis is similar to that of the general population,there is an increased risk of digestive tract cancers. Persistentor unexplained gastrointestinal symptoms in these patients shouldbe 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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