NY-ESO-1 expression in DCIS: A new predictor of good prognosis
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Published version
Author(s)
Type
Journal Article
Abstract
BACKGROUND: At present, it is difficult to predict which patients with ductal carcinoma-in-situ (DCIS) will subsequently develop frank invasive breast cancer (IDC). A recent survey by our group has shown that NY-ESO-1 and MAGEA are both expressed in DCIS. This study was aimed at determining whether expression of these antigens was related to the later development of IDC. RESULTS: 14 of 42 (33%) of patients developed invasive breast cancer during the follow up period. Only one of those DCIS cases that relapsed was positive for NYESO-1 at diagnosis. In contrast, DCIS samples of 15 of the 28 (54%) of those patients who remained disease-free expressed NY-ESO-1. (Permutation chi square p=0.0033). METHODS: We identified 42 patients with DCIS, and followed them up for more than 10 years. NY-ESO-1 and MAGEA were demonstrated by immunostaining as were CD8+ infiltrates on all sections together with the conventional markers, ER, PR, and HER2. CONCLUSIONS: Expression of NY-ESO-1 may predict those patients who will not subsequently develop invasive breast cancer and could therefore potentially be helpful in defining prognosis in patients with DCIS.
Date Issued
2017-04-05
Date Acceptance
2017-03-25
Citation
Oncoscience, 2017, 4 (3-4), pp.33-40
ISSN
2331-4737
Publisher
Impact Journals
Start Page
33
End Page
40
Journal / Book Title
Oncoscience
Volume
4
Issue
3-4
Copyright Statement
© 2017 Coombes et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License
(CC-BY), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source
are credited.
(CC-BY), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source
are credited.
Identifier
https://www.ncbi.nlm.nih.gov/pubmed/28540335
PII: 348
Subjects
CT antigen
breast cancer
ductal-carcinoma-in-situ (DCIS)
immunotherapy
prognosis
Publication Status
Published
Coverage Spatial
United States