Background: We examined the clinicopathologic profile of T1 cancers to dete
rmine whether palpable cancers are different from nonpalpable cancers.
Methods: A prospective database was reviewed. Palpable TI cancers were comp
ared with nonpalpable TI cancers. Initial significance was determined by ch
i (2) analysis. Factors found to be significant were then reanalyzed, contr
olling for tumor size by logistic or linear regression, as appropriate.
Results: Of 1263 TI cancers treated between 1981 and 2000, 857 (68%) were p
alpable and 401 (32%) were nonpalpable. Palpability correlated with patholo
gic tumor size, mitotic grade, nuclear grade, high S-phase, lymphovascular
invasion, nodal positivity, and lack of extensive intraductal component, mu
ltifocality, and multicentricity. There was no significant difference in es
trogen 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 can
cers, with a less diffuse growth pattern, higher metastatic potential, high
er proliferative activity, more nuclear abnormalities, and a worse prognosi
s.