期刊
BRITISH JOURNAL OF CANCER
卷 106, 期 8, 页码 1367-1373出版社
NATURE PUBLISHING GROUP
DOI: 10.1038/bjc.2012.85
关键词
breast cancer; HER2; EGFR; IGF1R; PTEN/PI3K/Akt pathway; trastuzumab resistance
类别
资金
- Fondo de Investigaciones Sanitarias (FIS) [PI06/0709, PI06/1495]
- Instituto Carlos III RTICCCFIS [RD06/0020/0015]
- Pfizer Laboratories
- Mutua Madrilena Foundation [448/2008]
- ROCHE Diagnostics-Sociedad Espanola de Anatomia Patologica (SEAP)
BACKGROUND: Trastuzumab resistance hampers its well-known efficacy to control HER2-positive breast cancer. The involvement of PI3K/Akt pathway in this mechanism is still not definitively confirmed. METHODS: We selected 155 patients treated with trastuzumab after development of metastasis or as adjuvant/neoadjuvant therapy. We performed immunohistochemistry for HER2, ER/PR, epidermal growth factor 1-receptor (EGFR), alpha-insulin-like growth factor 1-receptor (IGF1R), phosphatase and tensin homologue (PTEN), p110 alpha, pAkt, pBad, pmTOR, pMAPK, MUC1, Ki67, p53 and p27; mutational analysis of PIK3CA and PTEN, and PTEN promoter hypermethylation. RESULTS: We found 46% ER/PR-positive tumours, overexpression of EGFR (15%), alpha-IGF1R (25%), p110 alpha (19%), pAkt (28%), pBad (22%), pmTOR (23%), pMAPK (24%), MUC1 (80%), PTEN loss (20%), and PTEN promoter hypermethylation (20%). PIK3CA and PTEN mutations were detected in 17% and 26% tumours, respectively. Patients receiving adjuvant trastuzumab with alpha-IGF1R or pBad overexpressing tumours presented shorter progression-free survival (PFS) (all P <= 0.043). Also, p110a and mTOR overexpression, liver and brain relapses implied poor overall survival (OS) (all P <= 0.041). In patients with metastatic disease, decreased PFS correlated with p110 alpha expression (P = 0.024), whereas for OS were the presence of vascular invasion and EGFR expression (P <= 0.019; Cox analysis). CONCLUSION: Our results support that trastuzumab resistance mechanisms are related with deregulation of PTEN/PI3K/Akt/mTOR pathway, and/or EGFR and IGF1R overexpression in a subset of HER2-positive breast carcinomas. British Journal of Cancer (2012) 106, 1367-1373. doi: 10.1038/bjc.2012.85 www.bjcancer.com Published online 27 March 2012 (C) 2012 Cancer Research UK
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