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Oesophageal and gastric intestinal-type adenocarcinomas show same male predominance - due to 17 year delayed development in females
  1. Mohammad H Derakhshan (derakhshan68{at}
  1. University of Glasgow, United Kingdom
    1. Sarah Liptrot
    1. University of Glasgow, United Kingdom
      1. James Paul
      1. University of Glasgow, United Kingdom
        1. Ian L Brown
        1. University of Glasgow, United Kingdom
          1. Douglas Morrison
          1. University of Glasgow, United Kingdom
            1. Kenneth E.L. McColl (k.e.l.mccoll{at}
            1. University of Glasgow, United Kingdom


              Background & Aims: Upper gastrointestinal adenocarcinomas show an unexplained male predominance which is more apparent in oesophagus than stomach and in intestinal than diffuse histological subtype. We have conducted a population-based study to determine whether the gender phenomenon is primarily related to the anatomical site or the histological subtype

              Method & Materials: Of 3270 gastric and oesophageal cancers recorded in West of Scotland Cancer Registry, 1998-2002, 812 were randomly selected for detailed analysis. The Lauren histological subtype of adenocarcinoma was determined by reviewing 1204 original reports and 3241 biopsies.

              Results: Analysis included 405 non-cardia cancers, 173 cardia cancers and 209 oesophageal adenocarcinomas. Crude incidence rate of intestinal subtype was higher in males (23.86/ 100,000/ year) versus females (9.00/ 100,000/ year), giving M/F of 2.65 whereas diffuse subtype was similar for both genders (5.58 vs. 5.20 /100, 000/ year) yielding M/F of 1.07. The M/F ratios for oesophageal, cardia and non-cardia gastric cancer were 3.5, 2.0 and 1.6 respectively. Multiple logistic regression indicated that the odds of male gender was related to the histological subtype rather than anatomical location, (OR, 95% CI: 2.6, 1.78 - 3.9). Curve fitting of the age-specific incidence of intestinal subtype indicated that similar functions describe the rise in incidence with age in males and in females. However, the age-specific incidence of female intestinal type was delayed by 17.3 years. The M/F ratio of intestinal subtype was 3.41at age <50 years, peaked at 7.86 at age 50-59 and then showed a progressive decrease after 50-60 years of age.

              Conclusion: Male predominance of upper gastrointestinal adenocarcinoma is related to the intestinal histological subtype rather than tumour location and due to marked delayed development of this subtype in females prior to 50-60 years of age.

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