Abstract
Purpose: To assess patient and tumor characteristics associated with a complete pathologic response (pCR) in both the breast and axillary lymph node specimens and the outcome of patients found to have a pER after neoadjuvant chemotherapy for locally advanced breast cancer (LABC). Patients and Methods: Three hundred seventy-two LABC patients received treatment in two prospective neoadjuvant trials using four cycles of doxorubicin-containing chemotherapy. Patients had a total mastectomy with axillary dissection or segmental mastectomy and axillary dissection followed by four or more cycles of additional chemotherapy. Patients then received irradiation treatment of the chest-wall or breast and regional lymphatics. Median follow-up was 58 months (range, 8 to 99 months). Results: The initial nodal status, age, and stage distribution of patients with a pCR were not significantly different from those of patients with less than a pCR (P > .05). Patients with a pER had initial tumors that were more likely to be estrogen receptor (ER)-negative (P < .01), and anaplastic (P = .01) but of smaller size (P < .01) than those of patients with less than a pER. Upon multivariate analysis, the effects of ER status and nuclear grade were independent of initial tumor size. Sixteen percent of the patients in this study (n = 60) had a pathologic complete primary tumor response. Twelve percent of patients (n = 43) had no microscopic evidence of invasive cancer in their breast and axillary specimens. A pathologic complete primary tumor response was predictive of a complete axillary lymph node response (P < .01). The 5-year overall and disease-free survival rates were significantly higher in the group who had a pCR (89% and 87%, respectively) than in the group who had less than a pCR (64% and 58%, respectively; P < .01). Conclusion: Neoadjuvant chemotherapy has the capacity to completely clear the breast and axillary lymph nodes of invasive tumor before surgery. Patients with LABC who have a pER in the breast and axillary nodes have a significantly improved disease-free survival rate. However, a pER does not entirely eliminate recurrence. Further efforts should focus on elucidating the molecular mechanisms associated with this response.
Original language | English (US) |
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Pages (from-to) | 460-469 |
Number of pages | 10 |
Journal | Journal of Clinical Oncology |
Volume | 17 |
Issue number | 2 |
DOIs | |
State | Published - Feb 1999 |
ASJC Scopus subject areas
- Oncology
- Cancer Research