| Literature DB >> 24618694 |
Laura D Locati1, Federica Perrone2, Barbara Cortelazzi2, Martina Imbimbo1, Paolo Bossi1, Paolo Potepan3, Enrico Civelli3, Gaetana Rinaldi4, Pasquale Quattrone5, Lisa Licitra1, Silvana Pilotti2.
Abstract
Androgen-deprivation therapy (ADT) has been reported to be active in androgen receptor (AR)-expressing, relapsed/metastatic (RM), salivary gland cancers (SGCs). Abiraterone, an inhibitor of androgen synthesis, has recently been approved as a second-line treatment in hormone-resistant (HR) prostate cancer (PCa) patients. Two patients with AR-positive HR-RM adenocarcinoma, NOS of the salivary glands have been treated with abiraterone. This is the first time that this agent has been reported to be active in tumors other than HRPCa. Immunohistochemical analysis showed overexpression of EGFR, HER2, and HER3 in both untreated primary tumors. Sequencing analysis revealed a TP53 non-functional mutation in one case and a PIK3CA-activating mutation in the other. In conclusion, second line activity of ADT in AR-expressing, adenocarcinoma, NOS of salivary glands further strengthens the pathogenic and therapeutic role of AR signaling in AR-positive SGCs.Entities:
Keywords: HER3; PIK3CA; TP53; abiraterone; androgen deprivation therapy; androgen receptor; salivary gland cancers
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Year: 2014 PMID: 24618694 PMCID: PMC4049783 DOI: 10.4161/cbt.28410
Source DB: PubMed Journal: Cancer Biol Ther ISSN: 1538-4047 Impact factor: 4.742