| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
ORIGINAL ARTICLES |
From the Departments of Surgery (KAS, HS) and Preventive Medicine (RS), Norris Comprehensive Cancer Center, Keck School of Medicine, The University of Southern California, Los Angeles, California.
Correspondence: Address correspondence and reprint requests to: Kristin A. Skinner, MD, Norris Comprehensive Cancer Center, 1441 Eastlake Avenue, MS74, Los Angeles, CA 90033; Fax: 323-865-0119; E-mail: kskinner{at}hsc.usc.edu
Background: We examined the clinicopathologic profile of T1 cancers to determine whether palpable cancers are different from nonpalpable cancers.
Methods: A prospective database was reviewed. Palpable T1 cancers were compared with nonpalpable T1 cancers. Initial significance was determined by
2 analysis. Factors found to be significant were then reanalyzed, controlling for tumor size by logistic or linear regression, as appropriate.
Results: Of 1263 T1 cancers treated between 1981 and 2000, 857 (68%) were palpable and 401 (32%) were nonpalpable. Palpability correlated with pathologic tumor size, mitotic grade, nuclear grade, high S-phase, lymphovascular invasion, nodal positivity, and lack of extensive intraductal component, multifocality, and multicentricity. There was no significant difference in estrogen receptor, progesterone receptor or Her-2/neu status, ploidy, or DNA index. Breast cancer-specific survival was worse for patients with palpable cancers.
Conclusions: Palpable cancers are inherently different from nonpalpable cancers, with a less diffuse growth pattern, higher metastatic potential, higher proliferative activity, more nuclear abnormalities, and a worse prognosis.
Key Words: Palpable Nonpalpable Breast cancer Clinicopathologic features
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |