Abstract
It is now accepted that c-erbB2-gene amplification is correlated with poor clinical outcome for patients, mainly when axillary nodes are invaded. We have confirmed this result by multivariate analysis in 178 patients with non-inflammatory breast cancer followed up for a mean period of 6.8 years (SD, 1.6 years). In addition, we have shown that c-erbB2 amplification, found in 30 (17%) specimens, was associated with a high risk of multiple metastases developing simultaneously. In contrast, for the 67 patients with inflammatory breast carcinoma, the most aggressive type of breast carcinoma, the c-erbB2 amplification detected in 24 (36%) specimens was not found to be associated with a higher risk of death, suggesting that the c-erbB2 gene plays a different role in the progression of these 2 types of breast cancer. Furthermore, our data stress the importance of the methodological approach used to determine gene amplification. Although Southern blot hybridization is a tumour- and time-consuming method not easy to adopt in routine clinical practice, this method remains a reference quantitative method. (C) 1994 Wiley-Liss, Inc.
| Original language | English |
|---|---|
| Pages (from-to) | 763-768 |
| Number of pages | 6 |
| Journal | International Journal of Cancer |
| Volume | 58 |
| Issue number | 6 |
| Publication status | Published - 15 Sept 1994 |
Keywords / Materials (for Non-textual outputs)
- PROTEIN OVEREXPRESSION
- RECURRENT DISEASE
- INCREASED RISK
- FOLLOW-UP
- CANCER
- EXPRESSION
- C-ERBB-2
- ONCOGENE
- PROLIFERATION
- ONCOPROTEIN
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