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Merck

[Abiraterone acetate (AA): current guidelines of prescription of abiraterone].

Bulletin du cancer (2014-05-06)
Emilie Boissier, Yohann Loriot, Stéphane Vignot, Christophe Massard
ABSTRAKT

Abiraterone acetate (AA) is a selective inhibitor of cytochrom p450 (CYP)17 which is required for androgen biosynthesis, and can block the androgens synthesis by testicles, surrenals and intratumoral secretion. In phase I and II studies in patients with prostate cancer, therapy with AA 250-2000  mg once daily demonstrated reductions in prostate specific antigen (PSA), and/or circulating tumor cells (CTCs). In two large phase III trials in patients with metastatic castration resistant prostate cancer (CRPC) in post-docetaxel and pre-docetaxel setting, AA plus prednisone compared with placebo plus prednisone demonstrated a significant superior overall survival in post-docetaxel setting, and a superior radiological PFS in pre-docetaxel setting. Based of these results, AA is approved in metastatic CRPC patients in post-docetaxel setting or pre-docetaxel setting in 2013.

MATERIAŁY
Numer produktu
Marka
Opis produktu

Supelco
Prednisone, Pharmaceutical Secondary Standard; Certified Reference Material
Sigma-Aldrich
Docetaxel, purum, ≥97.0% (HPLC)
Sigma-Aldrich
Prednisone, ≥98%
USP
Prednisone, United States Pharmacopeia (USP) Reference Standard
Anhydrous Docetaxel, European Pharmacopoeia (EP) Reference Standard