© 1997 by Oxford University Press
Journal Of The National Cancer Institute, Vol 89, 442-446, Copyright © 1997 by Oxford University Press
AB Lowenfels, P Maisonneuve, EP DiMagno, Y Elitsur, LK Gates Jr, J Perrault and DC Whitcomb
BACKGROUND: Hereditary pancreatitis is an autosomal-dominant disease, with
a variable expression and an estimated penetrance of 80%. The gene for this
disease has recently been mapped to chromosome 7q35, and the defect is
believed to be caused by a mutation in the cationic trypsinogen gene. Acute
attacks of abdominal pain begin early in life and the disease often
progresses to chronic pancreatitis. Although the risk of pancreatic cancer
is thought to be increased in more common types of chronic pancreatitis,
the frequency of pancreatic cancer in the inherited type of pancreatitis is
uncertain. PURPOSE: The aim of this study was to assess the frequency of
pancreatic cancer and other tumors in patients with hereditary form of
pancreatitis. METHODS: To determine the natural history of hereditary
pancreatitis, we invited all members of the American Pancreatic Association
and the International Association of Pancreatology to participate in a
longitudinal study of this rare form of pancreatitis. The initial criteria
for patient eligibility were as follows: early age (< or = 30 years) at
onset of symptoms, positive family history, and absence of other causes.
From April 1995 through February 1996, 37 physicians from 10 countries
contributed medical records of 246 (125 males and 121 females) patients
thought to have hereditary pancreatitis as the most likely diagnosis. This
group included 218 patients where the diagnosis appeared to be highly
probable and 28 additional patients where the diagnosis of hereditary
pancreatitis was less certain: 25 patients who had relatively late onset of
disease and a positive family history and three patients with onset of
disease before age 30 years but with an uncertain family history. We
reviewed all causes of death and compared the observed to the expected
frequency of cancer in this historical cohort of patients with hereditary
pancreatitis. The strength of the association between pancreatitis and
pancreatic cancer was estimated by the standardized incidence ratio (SIR),
which is the ratio of observed pancreatic cancer cases in the cohort to the
expected pancreatic cancers in the background population, adjusted for age,
sex, and country. RESULTS: The mean age (+/- standard deviation [SD]) at
onset of symptoms of pancreatitis was 13.9 +/- 12.2 years. Compared with an
expected number of 0.150, eight pancreatic adenocarcinomas developed (mean
age +/- SD at diagnosis of pancreatic cancer: 56.9 +/- 11.2 years) during
8531 person-years of follow-up, yielding an SIR of 53 (95% confidence
interval [CI] = 23-105). The frequency of other tumors was not increased:
SIR = 0.7 (95% CI = 0.3-1.6). Eight of 20 reported deaths in the cohort
were from pancreatic cancer. Thirty members of the cohort have already been
tested for the defective hereditary pancreatitis gene: all 30 carry a
mutated copy of the trypsinogen gene. The transmission pattern of
hereditary pancreatitis was known for 168 of 238 patients without
pancreatic cancer and six of eight with pancreatic cancer. Ninety-nine of
the 238 patients without pancreatic cancer and six of the patients with
pancreatic cancer inherited the disease through the paternal side of the
family. The estimated cumulative risk of pancreatic cancer to age 70 years
in patients with hereditary pancreatitis approaches 40%. For patients with
a paternal inheritance pattern, the cumulative risk of pancreatic cancer is
approximately 75%. CONCLUSIONS: Patients with hereditary pancreatitis have
a high risk of pancreatic cancer several decades after the initial onset of
pancreatitis. A paternal inheritance pattern increases the probability of
developing pancreatic cancer.
REVIEWS
Hereditary pancreatitis and the risk of pancreatic cancer. International Hereditary Pancreatitis Study Group
Department of Surgery, New York Medical College, Valhalla 10595, USA.
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