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Incidence and possible pathogenesis of sentinel node micrometastases in ductal carcinoma in situ of the breast detected using molecular whole lymph node assay.

Authors :
Osako T
Iwase T
Kimura K
Masumura K
Horii R
Akiyama F
Osako, T
Iwase, T
Kimura, K
Masumura, K
Horii, R
Akiyama, F
Source :
British Journal of Cancer; 5/8/2012, Vol. 106 Issue 10, p1675-1681, 7p
Publication Year :
2012

Abstract

<bold>Background: </bold>The pathogenesis of lymph node metastases in preinvasive breast cancer – ductal carcinoma in situ (DCIS) – remains controversial. The one-step nucleic acid amplification (OSNA) assay is a novel molecular method that can assess a whole node and detect clinically relevant metastases. In this retrospective cohort study, we determined the performance of the OSNA assay in DCIS and the pathogenesis of node-positive DCIS.<bold>Methods: </bold>The subjects consisted of 623 patients with DCIS who underwent sentinel lymph node (SN) biopsy. Of these, 2-mm-sectioned nodes were examined using frozen-section (FS) histology in 338 patients between 2007 and 2009, while 285 underwent OSNA whole node assays between 2009 and 2011. The SN-positivity rate was compared between cohorts, and the characteristics of OSNA-positive DCIS were investigated.<bold>Results: </bold>The OSNA detected more cases of SN metastases than FS histology (12 out of 285, 4.2% vs 1 out of 338, 0.3%). Most of the metastases were micrometastases. The characteristics of high-risk DCIS (i.e., mass formation, size, grade, and comedo) and preoperative breast biopsy (i.e., methods or time to surgery) were not valid for OSNA assay–positive DCIS.<bold>Conclusion: </bold>The OSNA detects more SN metastases in DCIS than FS histology. Further examination of the primary tumours and follow-up of node-positive DCIS are needed to elucidate the pathogenesis. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00070920
Volume :
106
Issue :
10
Database :
Complementary Index
Journal :
British Journal of Cancer
Publication Type :
Academic Journal
Accession number :
104444407
Full Text :
https://doi.org/10.1038/bjc.2012.168