Prognostic and predictive factors in colorectal cancer

Aim: The aim of the thesis was to study prognostic and predictive factors in patients treated for colorectal cancer (CRC). Method: In paper I, a retrospective comparison was made between the patients treated in 1999 (n=180) with those treated in 2004 (n=175). During the period, a multidisciplinary team conference and an improved cooperation with the pathologists had been initiated. The focus of interest was the lymph node assessment, its’ development and how this affected clinical staging and treatment. In paper II, the lymph node diagnostics were studied in patients with stage III colon cancer 1999-2003 (n=265). Prognostic markers were evaluated along with the use of the lymph node ratio as a prognostic indicator to differentiate the risk assessment within the stage group. In paper III, single nucleotide pair (SNP) gene analyses was made for the metylentetrahydrofolate reduktase (MTHFR) gene polymorphism C677T in patients treated for colorectal cancer 1999-2006 (n=544). The functional polymorphisms were then correlated to pathology, stage, outcome and side effects of chemotherapy. Comparisons of genotype prevalence were made against a cohort of 299 blood donors as well as the pathology data of the other 1256 patients treated during this period. In paper IV, the presence of cyclin E in both tumour and mucosa was studied in 114 patients with stage I/II colon cancer treated 2003-2007. The expression was analyzed in both tumour and adjacent mucosa and the results were correlated to pathology, staging and prognosis. Results: In paper I, an improved lymph node assessment was shown to lead to stage migration and thus an increase of patients with stage III disease. A highly variable outcome in stage II associated to an inadequate assessment was also found. In paper II, stage III disease was found to have heterogeneous survival prognosis and the lymph node ratio was a significant marker for the outcome (p<0.001). In paper III, no correlations between polymorphism genotype and the risk of cancer or cancer stage were found. There was a significant correlation to the risk of suffering side-effects (p<0,05) and to the outcome in stage III colon cancer (p<0,003). In paper IV, cyclin E was found to be expressed in both full length form and shorter isoform in both tumour and adjacent mucosa. A high total expression of cyclin E correlated significantly to the risk of tumour recurrence (p