HER-2/NEU IN NODE-NEGATIVE BREAST-CANCER - PROGNOSTIC-SIGNIFICANCE OF OVEREXPRESSION INFLUENCED BY THE PRESENCE OF INSITU CARCINOMA

被引:435
作者
ALLRED, DC
CLARK, GM
TANDON, AK
MOLINA, R
TORMEY, DC
OSBORNE, CK
GILCHRIST, KW
MANSOUR, EG
ABELOFF, M
EUDEY, L
MCGUIRE, WL
机构
[1] UNIV TEXAS, HLTH SCI CTR, DEPT MED ONCOL, 7703 FLOYD CURL DR, SAN ANTONIO, TX 78284 USA
[2] UNIV TEXAS, HLTH SCI CTR, DEPT PATHOL, SAN ANTONIO, TX 78284 USA
[3] HOSP CLIN BARCELONA, BIOQUIM LAB, BARCELONA, SPAIN
[4] UNIV WISCONSIN, MADISON, WI 53706 USA
[5] CASE WESTERN RESERVE UNIV, METROHLTH MED CTR, CLEVELAND, OH 44106 USA
[6] JOHNS HOPKINS UNIV HOSP, CTR ONCOL, BALTIMORE, MD 21205 USA
[7] HARVARD UNIV, SCH MED, DANA FARBER CANC INST, BOSTON, MA 02115 USA
关键词
D O I
10.1200/JCO.1992.10.4.599
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Amplification and/or overexpression of the HER-2/neu oncogene have been shown to correlate with poor clinical outcome in patients with axillary node-positive breast cancer. In contrast, the prognostic significance of HER-2/neu in node-negative disease is controversial. This study was undertaken to evaluate further the relationship between HER-2/neu and clinical outcome in node-negative disease. Patients and Methods: Overexpression of HER-2/neu was evaluated by permanent-section immunohistochemistry in tumors from 613 patients with long-term clinical follow-up enrolled in the Intergroup Study 0011. Patients were stratified into low-risk (n = 307) and high-risk (n = 306) groups on the basis of tumor size and estrogen-receptor (ER) status. Low-risk patients were defined as having small (< 3 cm), ER-positive tumors and were observed without additional treatment after initial surgery. High-risk patients had either ER- negative or large (≥ 3 cm), ER-positive tumors and were randomized to be observed (n = 146) or to receive adjuvant chemotherapy (n = 160) after surgery. Results: The rate of HER-2/neu overexpression was 14.3% in all tumors combined and was higher in invasive-carcinomas with (21.5%) than without (11.2%) a significant noninvasive or in situ histologic component (P < .0001). There was no relationship between overexpression and clinical outcome in the natural history setting of combined low-risk and high-risk patients not receiving adjuvant therapy (n = 453). Based on the reasoning that the influence of HER-2/neu may have been obscured by high-risk features and/or the presence of noninvasive carcinoma, we also analyzed the subset of patients with low-risk lesions not containing a significant in situ component (n = 179). Patients of this group with HER-2/neu-positive tumors showed only 40% disease-free survival (DFS) at 5 years, compared with over 80% in patients with HER-2/neu-negative tumors (P < .0001). A similar inverse correlation was observed between overexpression and overall survival in the same group of patients (P = .0001). In a separate analysis involving patients receiving adjuvant chemotherapy, those with HER-2/neu-negative tumors showed significantly improved DFS in response to therapy compared with patients with HER-2/neu-positive tumors. Conclusion: Overexpression of HER-2/neu is associated with poor clinical outcome in a subset of node-negative patients with small, ER-positive, predominantly invasive tumors and may play a role in resistance to adjuvant chemotherapy.
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收藏
页码:599 / 605
页数:7
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