Prognostic significance of microsatellite instability in sporadic mucinouscolorectal cancers

Citation
L. Messerini et al., Prognostic significance of microsatellite instability in sporadic mucinouscolorectal cancers, HUMAN PATH, 30(6), 1999, pp. 629-634
Citations number
36
Categorie Soggetti
Research/Laboratory Medicine & Medical Tecnology","Medical Research Diagnosis & Treatment
Journal title
HUMAN PATHOLOGY
ISSN journal
00468177 → ACNP
Volume
30
Issue
6
Year of publication
1999
Pages
629 - 634
Database
ISI
SICI code
0046-8177(199906)30:6<629:PSOMII>2.0.ZU;2-8
Abstract
We investigated the prognostic significance of microsatellite instability ( MI) in 50 consecutive patients with sporadic mucinous colorectal cancer who had undergone only surgery. We evaluated MI and the pathological features with a possible prognostic value for each tumor, and the effect of the exam ined parameters on patients' outcome was statistically analyzed (univariate and multivariate analysis). All patients were followed-up for a minimum of 72 months or until death; in evaluating survival, only deaths of colorecta l cancer were considered. DNA extracted from tumor sections and the corresp onding normal tissue was analyzed by polymerase chain reaction at six micro satellite loci: D2S123, D3S1611, D3S49, D5S107, BAT26, BAT40. Alterations a t two or more loci were detected in 36% of cases (MI+ tumors). MI+ and MI- cancers differed significantly in the pattern of growth, and most MI+ tumor s showed an expanding type of growth (72.2%, P=.005). At univariate analysi s, improved survival rate was significantly associated with MI, as well as with the following parameters: expanding cancer growth, Dukes stage, and ab sence of venous invasion. Nevertheless, at multivariate analysis, only the pattern of cancer growth and Dukes stage were independent prognostic factor s, whereas the effect on survival of MI and venous invasion was found to be negligible. In our study, MIS and MI-cancers differ only on the pattern of growth; therefore, our data suggest that the better survival rate in mucin ous cancers with genomic instability is strictly related to their less aggr essive type of growth. Copyright (C) 1999 by W.B. Saunders Company.