Biological behaviour and clinical implications of micrometastases.
Affiliation
Departments of Academic Surgery and Medicine, National University of Ireland,, Cork University Hospital and Mercy Hospital, Cork, Ireland.Issue Date
2012-02-03T15:12:18ZMeSH
Biopsy, Needle/methodsBone Marrow Neoplasms/diagnosis
Breast Neoplasms/diagnosis
Colorectal Neoplasms/diagnosis
Enzyme-Linked Immunosorbent Assay/methods
Flow Cytometry
Head and Neck Neoplasms/diagnosis
Humans
Immunohistochemistry/methods
Lymphatic Metastasis/diagnosis
Melanoma/diagnosis/secondary
Neoplasm Metastasis/*diagnosis
Neoplastic Cells, Circulating
Neovascularization, Pathologic/physiopathology
Stomach Neoplasms/diagnosis
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Br J Surg. 2000 Dec;87(12):1629-39.Journal
The British journal of surgeryDOI
10.1046/j.1365-2168.2000.01606.xPubMed ID
11122176Abstract
BACKGROUND: The most important prognostic determinant in cancer is the identification of disseminated tumour burden (metastases). Micrometastases are microscopic (smaller than 2 mm) deposits of malignant cells that are segregated spatially from the primary tumour and depend on neovascular formation (angiogenesis) to propagate. METHODS: The electronic literature (1966 to present) on micrometastases and their implications in malignant melanoma and epithelial cancers was reviewed. RESULTS: Immunohistochemical techniques combined with serial sectioning offer the best accuracy for detection of nodal micrometastases. Molecular techniques should be reserved for blood samples or bone marrow aspirates. Detection of micrometastases in regional lymph nodes and/or bone marrow confers a poor prognosis in epithelial cancers. The concept of sentinel node biopsy combined with serial sectioning and dedicated screening for micrometastases may improve staging procedures. Strategies against angiogenesis may provide novel therapies to induce and maintain micrometastatic dormancy. CONCLUSION: The concept of micrometastases has resulted in a paradigm shift in the staging of epithelial tumours and our overall understanding of malignant processes.Language
engISSN
0007-1323 (Print)0007-1323 (Linking)
ae974a485f413a2113503eed53cd6c53
10.1046/j.1365-2168.2000.01606.x
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