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Lymph node status as a guide to selection of available prognostic markers in breast cancer: the clinical practice of the future?

Authors :
Elzagheid A
Kuopio T
Pyrhönen S
Collan Y
Source :
Diagnostic pathology [Diagn Pathol] 2006 Nov 08; Vol. 1, pp. 41. Date of Electronic Publication: 2006 Nov 08.
Publication Year :
2006

Abstract

Prognosticators evaluating survival in breast cancer vary in significance in respect to lymph node status. Studies have shown e.g. that HER2/neu immunohistochemistry or HER2/neu gene amplification analysis do perform well as prognosticators in lymph node positive (LN +) patients but are less valuable in lymph node negative (LN -) patients. We collected data from different studies and tried to evaluate the relative significance of different prognosticators in LN+/LN- patient groups. In LN+ patients HER2/neu and E-cadherin immunohistochemistry were the statistically most significant prognosticators followed by proliferation associated features (mitotic counts by SMI (standardised mitotic index) or MAI (mitotic activity index), or S-phase fraction). Bcl-2 immunohistochemistry was also significant but p53 and cystatin A had no significance as prognosticators. In LN- patients proliferation associated prognosticators (SMI, MAI, Ki-67 index, PCNA immunohistochemistry, S-phase fraction) are especially valuable and also Cathepsin D, cystatin A, and p53 are significant, but HER2/neu or bcl-2, or E-cadherin less significant or without significance. We find that in studies evaluating single prognosticators one should distinguish between prognosticators suitable for LN+ and LN- patients. This will allow the choice of best prognosticators in evaluating the prospects of the patient. The distinction between LN+ and LN- patients in this respect may also be of special value in therapeutic decisions.

Details

Language :
English
ISSN :
1746-1596
Volume :
1
Database :
MEDLINE
Journal :
Diagnostic pathology
Publication Type :
Academic Journal
Accession number :
17092354
Full Text :
https://doi.org/10.1186/1746-1596-1-41