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review of literature on clinical pancreatology - The Pancreapedia

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over 11.5 milli<strong>on</strong> individuals. Estimates were based <strong>on</strong> Poiss<strong>on</strong> regressi<strong>on</strong>. RRs <str<strong>on</strong>g>of</str<strong>on</strong>g> tumoursfor individuals with a parental history <str<strong>on</strong>g>of</str<strong>on</strong>g> pancreatic cancer were also estimated. <strong>The</strong> risk <str<strong>on</strong>g>of</str<strong>on</strong>g>pancreatic cancer was elevated in individuals with a parental history <str<strong>on</strong>g>of</str<strong>on</strong>g> cancers <str<strong>on</strong>g>of</str<strong>on</strong>g> the liver(RR 1.41; 95 % c<strong>on</strong>fidence interval 1.10 to 1.81), kidney (RR 1.37; 95 % c<strong>on</strong>fidence interval1.06 to 1.76), lung (RR 1.50; 95 % c<strong>on</strong>fidence interval 1.27 to 1.79) and larynx (RR 1.98; 95% c<strong>on</strong>fidence interval 1.19 to 3.28). Associati<strong>on</strong>s were also found between parental history <str<strong>on</strong>g>of</str<strong>on</strong>g>pancreatic cancer and cancers <str<strong>on</strong>g>of</str<strong>on</strong>g> the small intestine, col<strong>on</strong>, breast, lung, testis and cervix in<str<strong>on</strong>g>of</str<strong>on</strong>g>fspring. <strong>The</strong>re was an increased risk <str<strong>on</strong>g>of</str<strong>on</strong>g> pancreatic cancer associated with early-<strong>on</strong>setbreast cancer in siblings. Pancreatic cancer aggregates in families with several types <str<strong>on</strong>g>of</str<strong>on</strong>g>cancer. Smoking may c<strong>on</strong>tribute to the familial aggregati<strong>on</strong> <str<strong>on</strong>g>of</str<strong>on</strong>g> pancreatic and lung tumours,and the familial clustering <str<strong>on</strong>g>of</str<strong>on</strong>g> pancreatic and breast cancer could be partially explained byinherited mutati<strong>on</strong>s in the BRCA2 gene [329].DanmarkIt was reported the incidence rates <str<strong>on</strong>g>of</str<strong>on</strong>g> pancreatic cancer in Denmark during 61 years <str<strong>on</strong>g>of</str<strong>on</strong>g> dataregistrati<strong>on</strong>, from 1943 to 2003 and it was calculated age-standardized, period-specificincidence rates <str<strong>on</strong>g>of</str<strong>on</strong>g> pancreatic cancer. A total <str<strong>on</strong>g>of</str<strong>on</strong>g> 32,654 incident cases <str<strong>on</strong>g>of</str<strong>on</strong>g> pancreatic cancerwere evaluated (male-female ratio, 1.4). <strong>The</strong> age-standardized incidence rate <str<strong>on</strong>g>of</str<strong>on</strong>g> pancreaticcancer increased steadily in the beginning <str<strong>on</strong>g>of</str<strong>on</strong>g> the study period from 3.75/100,000 pers<strong>on</strong>yearsin 1943 to 1947 to the maximum <str<strong>on</strong>g>of</str<strong>on</strong>g> 9.96/100,000 pers<strong>on</strong>-years in 1968 to 1972 am<strong>on</strong>gmen and from 2.95 in 1943 to 1947 to the maximum <str<strong>on</strong>g>of</str<strong>on</strong>g> 7.04 in 1978 to 1982 am<strong>on</strong>g women.<strong>The</strong> incidence rates declined between 1968 to 1972 and 1988 to 1992 for men and between1978 to 1982 and 2003 for women. More than 40 percent <str<strong>on</strong>g>of</str<strong>on</strong>g> the tumors were located in thehead <str<strong>on</strong>g>of</str<strong>on</strong>g> the pancreas; 14 percent were localized, 21 percent were regi<strong>on</strong>ally spread, and 36percent were metastatic at the time <str<strong>on</strong>g>of</str<strong>on</strong>g> diagnosis. During the period 1978 to 2003, thepercentages <str<strong>on</strong>g>of</str<strong>on</strong>g> histologically or cytologically verified adenocarcinomas remained relativelysteady, approximately 30 percent [330].FranceIn 2006, a total number <str<strong>on</strong>g>of</str<strong>on</strong>g> 149,000 cancer deaths were observed in France, 88,500 in themale populati<strong>on</strong> and 60,500 in the female populati<strong>on</strong>. In 2005, the number <str<strong>on</strong>g>of</str<strong>on</strong>g> new diagnoses<str<strong>on</strong>g>of</str<strong>on</strong>g> cancer is estimated to be 319,000, 183,000 am<strong>on</strong>g men and 136,000 am<strong>on</strong>g women. Agestandardisedmortality rates are decreasing for most frequent cancer sites, at least in recentyears, the main excepti<strong>on</strong>s being lung in the female populati<strong>on</strong>, and pancreas in both maleand female populati<strong>on</strong>s [331].KoreaUsing the populati<strong>on</strong>-based cancer registry in Jejudo, it was found that Jejudo had lowerincidence in stomach cancer than other regi<strong>on</strong>s in Korea. <strong>The</strong> aim <str<strong>on</strong>g>of</str<strong>on</strong>g> <strong>on</strong>e study was toevaluate reas<strong>on</strong>s for this difference. Citrus is the leading agricultural producti<strong>on</strong> in Jejudo,suggesting that lower cancer incidence in Jejudo could be explained by citrus fruit intake. Itwas evaluated this hypothesis with quantitative systematic <str<strong>on</strong>g>review</str<strong>on</strong>g> (QSR). Stomach cancerincidence was significantly lower, with a summary odds ratio (SOR) after QSR <str<strong>on</strong>g>of</str<strong>on</strong>g> 0.72. Inadditi<strong>on</strong>, the SOR <str<strong>on</strong>g>of</str<strong>on</strong>g> pancreatic cancer tended to be lower at 0.83 (95 % c<strong>on</strong>fidence interval0.70 to 0.98). It was suggested that lower cancer incidence in Jejudo could be explained byintake <str<strong>on</strong>g>of</str<strong>on</strong>g> citrus fruits [332].Arctic pancreatic cancerLittle informati<strong>on</strong> is available <strong>on</strong> the incidence and mortality <str<strong>on</strong>g>of</str<strong>on</strong>g> cancer am<strong>on</strong>g the Aboriginalpopulati<strong>on</strong> in the Province <str<strong>on</strong>g>of</str<strong>on</strong>g> Québec, Canada. Cancer was likely rare in this populati<strong>on</strong>

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