Annals of Surgical Oncology Sign the Guestbook
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS

This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Schreiber, R. H.
Right arrow Articles by Cox, C. E.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Schreiber, R. H.
Right arrow Articles by Cox, C. E.

Annals of Surgical Oncology, Vol 6, Issue 1 95-101, Copyright © 1999 by Society of Surgical Oncology


ARTICLES

Microstaging of breast cancer patients using cytokeratin staining of the sentinel lymph node

R. H. Schreiber, S. Pendas, N. N. Ku, D. S. Reintgen, A. R. Shons, C. Berman, D. Boulware and C. E. Cox
Department of Surgery, University of South Florida, Tampa, USA.

BACKGROUND: Sentinel lymph node (SLN) mapping is an effective and accurate method of axillary nodal evaluation for metastatic disease. Cytokeratin (CK) immunohistochemical (IHC) staining of the SLN has found micrometastatic disease previously undetected by routine hematoxylin and eosin (H&E) stains. The purpose of this study is to determine the number of patients who were upstaged or microstaged, i.e., detected to have micrometastatic disease only by combined lymphatic mapping with CK IHC. METHODS: Two hundred and ten patients with newly diagnosed breast cancer underwent intraoperative lymphatic mapping using a combination of vital blue dye and technetium-labeled sulfur colloid. The excised sentinel lymph nodes were examined grossly, by imprint cytology, by standard H&E histology, and by IHC stains for CK. SLNs that were only CK positive were confirmed to be malignant by histologic examination. RESULTS: CK IHC staining was performed on 381 SLNs in 210 breast cancer patients. Forty-seven of 210 patients (22.4%) had positive nodes. Thirty of these 47 patients (63.8%) had both H&E- and CK-positive SLNs, and an additional 17 of the 47 positive patients (36.2%) had only CK-positive SLNs. Seventeen of the 180 patients (9.4%) who were negative on H&E staining were upstaged by CK IHC staining of malignant cells in the SLN. Comparison of tumor size with the total number of node-positive patients demonstrated that 16 of 30 node-positive T0 and T1 patients (53.5%) and 22 of 39 nodes (56.4%) were upstaged by CK IHC staining. T2 and T3 patients were less frequently upstaged by cytokeratin analysis of lymph nodes. Only one of 17 node-positive patients (5.9%) and seven of 34 nodes (20.6%) in patients with T2 and T3 tumors were upstaged. CONCLUSION: CK IHC staining of SLNs shifted 9.4% of patients from stage I to stage II. There was a significant upstaging influence noted in patients with tumor sizes under 2 cm. This microstaging shift or upstaging may account for the significant proportion of stage I breast cancer treatment failures. Microstaging of the SLNs using more sensitive assays may help identify a subgroup of patients with invasive breast cancer who would benefit from systemic adjuvant treatment, while sparing a disease-free subset of patients the additional risks of toxic adjuvant chemotherapy.


This article has been cited by other articles:


Home page
Clin. Cancer Res.Home page
G.-C. Hsu, C.-H. Ku, J.-C. Yu, C.-B. Hsieh, C.-P. Yu, and T.-Y. Chao
Application of intraoperative ultrasound to nonsentinel node assessment in primary breast cancer.
Clin. Cancer Res., June 15, 2006; 12(12): 3746 - 3753.
[Abstract] [Full Text] [PDF]


Home page
Ann. Surg. Oncol.Home page
K. Dowlatshahi, M. Fan, J. M. Anderson, and K. J. Bloom
Occult Metastases in Sentinel Nodes of 200 Patients With Operable Breast Cancer
Ann. Surg. Oncol., September 1, 2001; 8(8): 675 - 681.
[Abstract] [Full Text] [PDF]


Home page
Arch SurgHome page
S. L. Wong, M. J. Edwards, C. Chao, T. M. Tuttle, R. D. Noyes, C. Woo, P. B. Cerrito, K. M. McMasters, and for the University of Louisville Breast Cancer Sen
Predicting the Status of the Nonsentinel Axillary Nodes: A Multicenter Study
Arch Surg, May 1, 2001; 136(5): 563 - 568.
[Abstract] [Full Text] [PDF]


Home page
Ann. Surg. Oncol.Home page
P. J. Tanis, R. P. A. Boom, H. S. Koops, I. F. Faneyte, J. L. Peterse, O. E. Nieweg, E. J. T. Rutgers, A. T. M. G. Tiebosch, and B. B. R. Kroon
Frozen Section Investigation of the Sentinel Node in Malignant Melanoma and Breast Cancer
Ann. Surg. Oncol., April 1, 2001; 8(3): 222 - 226.
[Abstract] [Full Text] [PDF]


Home page
Ann. Surg. Oncol.Home page
J. M. Kane III, S. B. Edge, J. S. Winston, N. Watroba, and T. C. Hurd
Intraoperative Pathologic Evaluation of a Breast Cancer Sentinel Lymph Node Biopsy as a Determinant for Synchronous Axillary Lymph Node Dissection
Ann. Surg. Oncol., April 1, 2001; 8(4): 361 - 367.
[Abstract] [Full Text] [PDF]


Home page
Ann. Thorac. Surg.Home page
M. J. Liptay, G. A. Masters, D. J. Winchester, B. L. Edelman, B. J. Garrido, T. R. Hirschtritt, R. M. Perlman, and W. A. Fry
Intraoperative radioisotope sentinel lymph node mapping in non-small cell lung cancer
Ann. Thorac. Surg., August 1, 2000; 70(2): 384 - 389.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 1999 by the Society of Surgical Oncology.