Comparison of HER-2 status between primary breast cancer and corresponding distant metastatic sites

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Abstract

Background: The humanized anti-HER-2 monoclonal antibody trastuzumab (Herceptin®) is a new treatment modality for metastastic breast cancer, the efficacy of which is directly correlated with the HER-2 status of the tumour, evaluated either by immunohistochemistry (IHC) and/or by fluorescence in situ hybridisation (FISH). This analysis is generally performed on the primary tumour. There are few data regarding the HER-2 status in the corresponding distant metastases. Methods: HER-2 status in 107 patients with a primary breast tumour and at least one distant metastatic lesion was analysed by IHC and FISH. Results: We found similar levels of amplification (25% and 24%) and overexpression (13% and 19%) of HER-2 in primary and metastatic samples, respectively. Among paired primary/metastatic tumours, six (6%) showed discordance by HercepTest™ (n = 100): all six cases showed greater Her-2 over-expression in the metastatic tissue. By FISH (n = 68), five (7%) cases were discordant: two cases were amplified in the primary tumour but not in the metastasis, and three samples showed amplification in the metastasis but not in the primary. Finally, we analysed HER-2 status in different metastatic lesions from 17 patients that had at least two distant metastatic sites. Discordance between different sites from the same patient was 18% by IHC and 19% by FISH. Conclusions: Between the paired primary tumour and distant metastatic lesions, 94% and 93% of samples had concordant HER-2 status when analysed by IHC or FISH, respectively. These results do not support routine determination of HER-2 on metastatic sites, particularly when FISH results from the primary tumour are available.

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Larsimont, D., Gancberg, D., Di Leo, A., Cardoso, F., Rouas, G., Pedrocchi, M., … Piccart, M. J. (2002). Comparison of HER-2 status between primary breast cancer and corresponding distant metastatic sites. Annals of Oncology, 13(7), 1036–1043. https://doi.org/10.1093/annonc/mdf252

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