Impact of multicentricity on clinical outcome in patients with T1-2, N0-1,M0 breast cancer

Citation
G. Vlastos et al., Impact of multicentricity on clinical outcome in patients with T1-2, N0-1,M0 breast cancer, ANN SURG O, 7(8), 2000, pp. 581-587
Citations number
28
Categorie Soggetti
Oncology
Journal title
ANNALS OF SURGICAL ONCOLOGY
ISSN journal
10689265 → ACNP
Volume
7
Issue
8
Year of publication
2000
Pages
581 - 587
Database
ISI
SICI code
1068-9265(200009)7:8<581:IOMOCO>2.0.ZU;2-7
Abstract
Background: The objective was to determine the impact of multicentric breas t cancer on recurrence and survival and to evaluate the current tumor, node , metastasis staging system recommendations for multicentricity in the brea st. Methods: This study included 284 nonpregnant patients with T1-2, N0-1, M0 b reast cancer, without previous cancer, who were treated by modified radical mastectomy followed by doxorubicin-based adjuvant chemotherapy. Clinical a nd pathological data were collected retrospectively and survival was calcul ated from the date of initial diagnosis using the Kaplan-Meier method. Results: The median follow-up time was 8 years (range, 0.3-24.0), and the m edian age was 47 years (range, 23-76). The median clinical size of the inde x tumor was 2.5 cm. In 17% of patients, the clinical nodal status was N1. I n 84% of patients, pathology of the index lesion was invasive ductal +/- in situ. Multicentric breast cancer was detected in 60 patients (21%): 30 pat ients with two lesions, 13 patients with three lesions, and 17 patients wit h four or more lesions. Locoregional recurrence, contralateral breast cance r, distant metastasis, and survival (disease-specific and disease-free) wer e similar in both groups of multicentric versus unicentric breast tumors. T here was a significant difference between groups in estrogen receptor and a xillary lymph node positivity, but these did not contribute significantly t o outcome on multivariate analysis. Conclusions: Multicentricity does not increase the risk of poor outcomes in patients with early-stage breast cancer. This supports the current recomme ndations of the tumor, node, metastasis staging system that tumor size shou ld be based on the diameter of the largest lesion in patients with multicen tric breast cancer.