P53 overexpression in colorectal metastases confined to the liver and outcome of liver resection

Citation
J. Heisterkamp et al., P53 overexpression in colorectal metastases confined to the liver and outcome of liver resection, HEP-GASTRO, 46(30), 1999, pp. 3109-3114
Citations number
35
Categorie Soggetti
Gastroenerology and Hepatology","da verificare
Journal title
HEPATO-GASTROENTEROLOGY
ISSN journal
01726390 → ACNP
Volume
46
Issue
30
Year of publication
1999
Pages
3109 - 3114
Database
ISI
SICI code
0172-6390(199911/12)46:30<3109:POICMC>2.0.ZU;2-6
Abstract
BACKGROUND/AIMS: The results of hepatic surgery for colorectal metastases a re distorted by the high incidence of recurrence, despite an apparently rad ical resection. Selection of high-risk patients is a mandatory step towards effective application of neo-adjuvant chemotherapy. In this study, express ion of the tumor suppresser gene p53 in colorectal liver metastases was cor related with recurrence after resection. METHODOLOGY: In a retrospective case-series p53 expression was assessed usi ng standard immunohistochemical methods in the paraffin-embedded specimens of 45 liver resections for colorectal metastases, performed in 43 patients in a single institution between '86 and '96. Hospital and office charts wer e reviewed and follow-up was completed with a General Physicians' questionn aire in October '97. Relapse-free and cancer-specific survival from diagnos is of hepatic metastases were assessed and compared for p53+ and p53- group s. RESULTS: Median survival was 36 months with an estimated 5-year cancer-spec ific survival of 43% (95% confidence interval 35%-51%). Relapse-free and ca ncer-specific survival were not significantly different between p53+ (n=24, 53%) and p53- (n=21) groups (P=0.86 and P=0.91 respectively). P53 expressi on was not associated with other potential predictors, which were not of pr edictive value either. CONCLUSIONS: Patients at risk for recurrent disease following partial hepat ectomy for colorectal metastases cannot be identified by p53 expression.