2013
DOI: 10.1038/bjc.2013.446
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Antitumour activity of abiraterone and diethylstilboestrol when administered sequentially to men with castration-resistant prostate cancer

Abstract: Background:Abiraterone is a standard treatment for men with castration-resistant prostate cancer (CRPC). We evaluated the antitumour activity of abiraterone following the synthetic oestrogen diethylstilboestrol (DES).Methods:Castration-resistant prostate cancer patients treated with abiraterone were identified. Demographics, response variables and survival data were recorded.Results:Two-hundred and seventy-four patients received abiraterone, 114 (41.6%) after DES. Pre-chemotherapy abiraterone resulted in ⩾50% … Show more

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Cited by 19 publications
(18 citation statements)
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“…Our report observed PSA declines ⩾50% in 28.4% of 81 patients treated with AA after DES and docetaxel and radiological responses in 25% of patients (Omlin et al , 2013). The differences of these two reports could be explained by the post hoc nature of the analyses and the differences in use of steroids.…”
mentioning
confidence: 52%
“…Our report observed PSA declines ⩾50% in 28.4% of 81 patients treated with AA after DES and docetaxel and radiological responses in 25% of patients (Omlin et al , 2013). The differences of these two reports could be explained by the post hoc nature of the analyses and the differences in use of steroids.…”
mentioning
confidence: 52%
“…Beside NAAs, with CAB a novel taxane has also entered clinical practice 10,11. CAB has been approved for the treatment of mCRPC in the post-docetaxel setting as a 2 nd line treatment and is currently investigated within the FIRSTANA trial as 1 st line treatment option at different dose levels.…”
Section: Discussionmentioning
confidence: 99%
“…[26][27][28] In patients who were treated with ENZ after treatment with docetaxel had failed, the use of third-line AA was associated with efficacy that was inferior to the reverse sequence analyzed herein. [29][30][31] Current guidelines do not suggest any specific agent after docetaxel and either AA or ENZ as second-line therapy. Current research is on optimizing the better sequence or the best combination of hormonal agents after first-line docetaxel treatment.…”
Section: Discussionmentioning
confidence: 99%