Previous studies of molecular prognostic markers following resection for exocrine pancreatic cancer have produced conflicting results. Our aim was to undertake a comprehensive analysis of potentially useful molecular markers in a large, multicentre patient population and to compare these markers with standard pathological prognostic variables. Formalin‐fixed, paraffin‐embedded specimens of pancreatic ductal adenocarcinoma were analysed from 157 patients [100 men and 57 women with a median (range) age of 60 (33–77) years] who had undergone pancreatectomy. Immunohistochemistry was used to detect expression of p16INK4, p53, p21WAF1, cyclin D1, erbB‐2 and erbB‐3. Mutations in codons 12 and 13 of the K‐ras oncogene were detected by SSCP and sequencing following DNA extraction and amplification by PCR. The median (range) survival post‐resection was 12.5 (3–83) months. Abnormalities of p16INK4, p53, p21WAF1, cyclin D1, erbB‐2 and erbB‐3 expression were found in 87%, 41%, 75%, 72%, 33% and 57% of cases, respectively. There was no significant correlation between expression of any of these markers and patient survival. K‐ras mutations were found in 73 (75%) of 97 cases with amplifiable DNA. The presence of K‐ras mutation alone did not correlate with survival, but there were significant differences in survival according to the type of K‐ras mutation (p = 0.0007). Reduced survival was found in patients with GaT, cGT and GcT K‐ras mutations compared to GtT, aGT and GaC mutations. In conclusion, survival was associated with type of K‐ras mutation but not expression of p16INK4, p53, p21WAF1, cyclin D1, erbB‐2 and erbB‐3. Int. J. Cancer 89:469–474, 2000. © 2000 Wiley‐Liss, Inc.

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Cytogenetic investigation of nine pancreatic carcinomas revealed structural rearrangements of chromosome 19 in eight cases, resulting in a high frequency of 19p losses and 19q gains. To characterize these imbalances further, we performed fluorescence in situ hybridization (FISH) analysis with 12 mapped and evenly distributed cosmids. The FISH study not only verified the cytogenetic findings but also disclosed additional chromosome 19 aberrations not detected by chromosome banding analysis. Seven carcinomas displayed 19p losses, always including 19p13.3, either through partial‐ or whole‐arm deletions. Six cases showed gain of 19q, usually as one to two copies above the ploidy level. In one case, a high level of amplification in 19q13.1 was seen. The commonly overrepresented segment was 19q13.1‐13.2. These results suggest that genes of importance in the development of pancreatic carcinomas are located in 19p13.3 and 19q13.1‐13.2. Genes Chromosomes Cancer 21:8–16, 1998. © 1998 Wiley‐Liss, Inc.