Prognostic significance of free gastrointestinal tumor cells in peritoneallavage detected by immunocytochemistry and polymerase chain reaction

Citation
R. Broll et al., Prognostic significance of free gastrointestinal tumor cells in peritoneallavage detected by immunocytochemistry and polymerase chain reaction, LANG ARCH S, 386(4), 2001, pp. 285-292
Citations number
31
Categorie Soggetti
Surgery
Journal title
LANGENBECKS ARCHIVES OF SURGERY
ISSN journal
14352443 → ACNP
Volume
386
Issue
4
Year of publication
2001
Pages
285 - 292
Database
ISI
SICI code
1435-2443(200107)386:4<285:PSOFGT>2.0.ZU;2-Q
Abstract
Aims: The aim of our study was to identify tumor cells in peritoneal lavage comparatively with immunocytochemistry (ICC) and half-nested reverse trans criptase-polymerase chain reaction (RT PCR) using carcinoembryonic antigen (CEA) as marker and to evaluate their prognostic significance. Patients and methods: In 75 patients who underwent surgery for a carcinoma of the color ectum (n=49), stomach (n=17) or pancreas (n=9) and 13 patients with an abdo minal aortic aneurysm (control group) the abdomen was irrigated with saline solution immediately after laparotomy. Cells were separated by Ficoll-dens ity centrifugation and divided into 2 equal volumes for ICC and RT PCR. For ICC cells were spun onto slides by cytospin centrifugation and stained wit h a monoclonal antibody (mab) against CEA using the APAAP method. For RT PC R total RNA was extracted from the cells, transcribed into cDNA and amplifi ed with CEA-specific primers. Lavages of 13 patients with an abdominal aort ic aneurysm and blood samples of 6 healthy donors served as controls. Resul ts: Immunostained tumor cells were found in peritoneal lavage in 23% (17/75 ) of all patients, whereas 63% (47/75) of patients gave a positive result b y RT PCR analysis. In the control group (n=13) no patient presented with tu mor cells in ICC, however 5 of 13 (38%) showed amplified CEA-mRNA by RT-PCR , and so did one of six blood samples. Using ICC technique, we found signif icant correlations between detection rates and pT, pN-, pM-categories as we ll as tumor stage. On the contrary, by RT PCR significant correlations were observed only between pT- and pM-categories and detection rates. Detection of tumor cells in peritoneal lavage with both techniques was associated wi th poor prognosis. Moreover, these tumor cells are an independent prognosti c factor and may have an influence on the development of peritoneal carcino matosis. Conclusion: ICC is a useful method for detection of tumor cells in peritoneal lavage. In contrast, half-nested RT-PCR cannot be recommended, as the detection rates are unproportionally high, obviously as a result of CEA-mRNA expression in nontumor cells.