Seriate cytology vs molecular analysis of peritoneal washing to improve gastric cancer cells detection.


Journal

Diagnostic cytopathology
ISSN: 1097-0339
Titre abrégé: Diagn Cytopathol
Pays: United States
ID NLM: 8506895

Informations de publication

Date de publication:
Jul 2019
Historique:
received: 06 12 2018
revised: 06 02 2019
accepted: 15 02 2019
pubmed: 2 3 2019
medline: 22 11 2019
entrez: 2 3 2019
Statut: ppublish

Résumé

Intraperitoneal malignant cells detection in patients with gastric cancer is associated with a significant decrease in overall survival. The overall accuracy of cytological examination of peritoneal lavages, however, is quite low, and intraperitoneal recurrence has been observed even in patients with negative cytology. Immunocytochemistry and molecular techniques have been investigated to improve high-risk patients' identification with variable results. The aim of this study was to compare the performance of different laboratory methods applied to peritoneal washing, to improve the cytological identification of malignant cells. We prospectively evaluated 21 patients who underwent surgery and peritoneal lavage for gastric cancer. Among them, 18 had negative cytology and three were positive for malignant cells. For each patient, immunohistochemistry with BerEP4 antibody was performed on seriate sections of cellblock preparation at different levels, using the method reported for sentinel nodes in other types of cancer. Paired frozen quotes of washing fluids were evaluated by qRT-PCR with primer for mRNA of Ceacam5. In 4 of 18 patients with previous negative routine cytology, isolated neoplastic cells in seriate sections of the cellblock inclusion have been found. Results showed to be coherent with molecular analysis for CEA mRNA. The sensitivity and specificity of peritoneal washing analyses should be notably improved by immunohistochemistry applied to multilevel cellblock sectioning. The method is less expensive and more widely applicable than molecular analysis, in each laboratory setting. This approach allows detection of minimum peritoneal seeding in patients with gastric cancer.

Sections du résumé

BACKGROUND BACKGROUND
Intraperitoneal malignant cells detection in patients with gastric cancer is associated with a significant decrease in overall survival. The overall accuracy of cytological examination of peritoneal lavages, however, is quite low, and intraperitoneal recurrence has been observed even in patients with negative cytology. Immunocytochemistry and molecular techniques have been investigated to improve high-risk patients' identification with variable results. The aim of this study was to compare the performance of different laboratory methods applied to peritoneal washing, to improve the cytological identification of malignant cells.
METHODS METHODS
We prospectively evaluated 21 patients who underwent surgery and peritoneal lavage for gastric cancer. Among them, 18 had negative cytology and three were positive for malignant cells. For each patient, immunohistochemistry with BerEP4 antibody was performed on seriate sections of cellblock preparation at different levels, using the method reported for sentinel nodes in other types of cancer. Paired frozen quotes of washing fluids were evaluated by qRT-PCR with primer for mRNA of Ceacam5.
RESULTS RESULTS
In 4 of 18 patients with previous negative routine cytology, isolated neoplastic cells in seriate sections of the cellblock inclusion have been found. Results showed to be coherent with molecular analysis for CEA mRNA.
CONCLUSION CONCLUSIONS
The sensitivity and specificity of peritoneal washing analyses should be notably improved by immunohistochemistry applied to multilevel cellblock sectioning. The method is less expensive and more widely applicable than molecular analysis, in each laboratory setting. This approach allows detection of minimum peritoneal seeding in patients with gastric cancer.

Identifiants

pubmed: 30821430
doi: 10.1002/dc.24165
doi:

Substances chimiques

Biomarkers, Tumor 0
CEACAM5 protein, human 0
Carcinoembryonic Antigen 0
GPI-Linked Proteins 0
human epithelial antigen-125 0

Types de publication

Comparative Study Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

670-674

Informations de copyright

© 2019 Wiley Periodicals, Inc.

Auteurs

Chiara Taffon (C)

Pathology Unit, University Hospital Campus Bio-Medico, Rome, Italy.

Isabella Giovannoni (I)

Pathology Unit, University Hospital Campus Bio-Medico, Rome, Italy.

Pamela Mozetic (P)

International Clinical Research Center, St. Anne's University Hospital, Brno, Czechia.

Gabriella Teresa Capolupo (GT)

Surgery Unit, University Hospital Campus Bio-Medico, Rome, Italy.

Vincenzo La Vaccara (V)

Surgery Unit, University Hospital Campus Bio-Medico, Rome, Italy.

Cristina Cinque (C)

Pathology Unit, University Hospital Campus Bio-Medico, Rome, Italy.

Chiara Caricato (C)

School of Medicine, Catholic University of the Sacred Heart, Rome, Italy.

Alberto Rainer (A)

Tissue Engineering Unit, Università Campus Bio-Medico di Roma, Rome, Italy.

Giovanni Zelano (G)

Institute of Human Anatomy and Cell Biology, Catholic University of the Sacred Heart, Rome, Italy.

Anna Crescenzi (A)

Pathology Unit, University Hospital Campus Bio-Medico, Rome, Italy.

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Classifications MeSH