Literature DB >> 7557136

Micrometastases in bone marrow of patients undergoing "curative" surgery for gastrointestinal cancer.

G C O'Sullivan1, J K Collins, F O'Brien, B Crowley, K Murphy, G Lee, F Shanahan.   

Abstract

BACKGROUND & AIMS: Immunohistochemical detection of bone marrow micrometastases has been reported as a prognostic marker in colorectal cancer. The aims of this study were to evaluate the potential advantage of flow cytometry as an objective method of identifying and quantifying micrometastatic deposits within bone marrow and to determine the prevalence and quantity of micrometastases in patients undergoing surgery for gastrointestinal cancers.
METHODS: Flow cytometry was first validated by a controlled "spike" experiment in which varying numbers of neoplastic epithelial cells were added to bone marrow, and cytometry was performed in a blinded fashion. Three neoplastic cell lines (colonic and esophageal) with varying degrees of expression of cytokeratin-18 were used. Epithelial cells were detected by dual staining with fluorescence-labeled, monoclonal anti-cytokeratin, and propidium iodide.
RESULTS: Cytometry reproducibly detected the presence of > or = 10 neoplastic cells per 10(5) marrow cells. Micrometastases were found in 20%-30% of patients undergoing potentially curative resection of colorectal and gastroesophageal adenocarcinomas. There was a trend toward increasing positivity for marrow deposits with advanced Dukes' staging of colorectal cancer.
CONCLUSIONS: Flow cytometric assessment of bone marrow is a reliable, objective, and quantitative method of detecting micrometastatic deposits found in a substantial subset of patients undergoing surgery for gastrointestinal adenocarcinomas.

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Year:  1995        PMID: 7557136     DOI: 10.1016/0016-5085(95)90641-x

Source DB:  PubMed          Journal:  Gastroenterology        ISSN: 0016-5085            Impact factor:   22.682


  7 in total

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2.  Detection of bone marrow micrometastases in the rib marrow of head and neck cancer patients: a prospective pilot study.

Authors:  Liam J Skinner; Brendan J Conlon; John D Russell; Gerald C O'sullivan; Tadhg P O'dwyer
Journal:  Eur Arch Otorhinolaryngol       Date:  2004-06-09       Impact factor: 2.503

3.  A prospective study of circulating mutant KRAS2 in the serum of patients with colorectal neoplasia: strong prognostic indicator in postoperative follow up.

Authors:  B M Ryan; F Lefort; R McManus; J Daly; P W N Keeling; D G Weir; D Kelleher
Journal:  Gut       Date:  2003-01       Impact factor: 23.059

4.  Micrometastases: marker of metastatic potential or evidence of residual disease?

Authors:  G C O'Sullivan; J K Collins; J Kelly; J Morgan; M Madden; F Shanahan
Journal:  Gut       Date:  1997-04       Impact factor: 23.059

5.  Prognostic value of postoperative detection of blood circulating tumor cells in patients with colorectal cancer operated on for cure.

Authors:  Xavier Bessa; Virgínia Piñol; Sergi Castellví-Bel; Elena Piazuelo; Antonio M Lacy; J Ignasi Elizalde; Josep M Piqué; Antoni Castells
Journal:  Ann Surg       Date:  2003-03       Impact factor: 12.969

6.  Detection of colonic cells in peripheral blood of colorectal cancer patients by means of reverse transcriptase and polymerase chain reaction.

Authors:  A Castells; L Boix; X Bessa; L Gargallo; J M Piqué
Journal:  Br J Cancer       Date:  1998-11       Impact factor: 7.640

7.  The presence of bone marrow cytokeratin-immunoreactive cells does not predict outcome in gastric cancer patients.

Authors:  G de Manzoni; G Pelosi; F Pavanel; A Di Leo; C Pedrazzani; E Durante; C Cordiano; F Pasini
Journal:  Br J Cancer       Date:  2002-04-08       Impact factor: 7.640

  7 in total

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