Abiraterone, Orteronel, Enzalutamide and Docetaxel: Sequential or Combined Therapy?

Objective: To summarize the current therapeutic status using chemotherapeutic agent docetaxel and endocrine therapeutic agents (ARAT, abiraterone, orteronel or enzalutamide) for the treatment of metastatic castration-resistant prostate cancer (mCRPC), including sequential therapy and combined therap...

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Main Authors: Ming-kun Chen (Author), Zhi-jian Liang (Author), Dao-Sheng Luo (Author), Kang-yi Xue (Author), De-ying Liao (Author), Zheshen Li (Author), Yuzhong Yu (Author), Zhe-Sheng Chen (Author), Shan-Chao Zhao (Author)
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Published: Frontiers Media S.A., 2022-02-01T00:00:00Z.
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042 |a dc 
100 1 0 |a Ming-kun Chen  |e author 
700 1 0 |a Ming-kun Chen  |e author 
700 1 0 |a Zhi-jian Liang  |e author 
700 1 0 |a Zhi-jian Liang  |e author 
700 1 0 |a Dao-Sheng Luo  |e author 
700 1 0 |a Kang-yi Xue  |e author 
700 1 0 |a Kang-yi Xue  |e author 
700 1 0 |a De-ying Liao  |e author 
700 1 0 |a De-ying Liao  |e author 
700 1 0 |a Zheshen Li  |e author 
700 1 0 |a Yuzhong Yu  |e author 
700 1 0 |a Zhe-Sheng Chen  |e author 
700 1 0 |a Shan-Chao Zhao  |e author 
700 1 0 |a Shan-Chao Zhao  |e author 
700 1 0 |a Shan-Chao Zhao  |e author 
245 0 0 |a Abiraterone, Orteronel, Enzalutamide and Docetaxel: Sequential or Combined Therapy? 
260 |b Frontiers Media S.A.,   |c 2022-02-01T00:00:00Z. 
500 |a 1663-9812 
500 |a 10.3389/fphar.2022.843110 
520 |a Objective: To summarize the current therapeutic status using chemotherapeutic agent docetaxel and endocrine therapeutic agents (ARAT, abiraterone, orteronel or enzalutamide) for the treatment of metastatic castration-resistant prostate cancer (mCRPC), including sequential therapy and combined therapy, to promote the consensus on the optimal regimen for achieving superior treatment efficacy.Methods: Through literature search in PubMed, articles with the following relevant keywords were collected and anlyzed: CRPC, abiraterone, orteronel and enzalutamide, median survival, overall survival, prostate specific antigen (PSA), PSA response rate and median radiologic progression-free survival.Results: Fifty-eight articles were obtained and analyzed in this review. These articles included androgen axis-targeting agents after docetaxel, docetaxel after androgen axis-targeting agents, Triple sequential and combination therapy, covering four current drugs for mCRPC treatment: docetaxel, abiraterone, orteronel, and enzalutamide. It was found that there may be some cross-resistance between androgen axis-targeting agents, which will reduce the efficacy of subsequent drug treatment. Although neither of the studies of using combination therapy showed serious drug toxicity, the efficacy of sequential therapy was not as good as expected. Most adverse reactions after treatment were reported to be level 1-2.Conclusion: Based on the results of the current studies, abiraterone followed by enzalutamide treatment is the best sequential treatment for most docetaxel-naïve patients. This treatment achieves not only good OS, but also PFS and PSA response rates. In addition, for patients who have previously failed docetaxel treatment, enzalutamide is the best choice as the subsequent treatment. 
546 |a EN 
690 |a metastatic castration-resistant prostate cancer 
690 |a sequential therapy 
690 |a combined therapy 
690 |a docetaxel 
690 |a abiraterone 
690 |a orteronel 
690 |a Therapeutics. Pharmacology 
690 |a RM1-950 
655 7 |a article  |2 local 
786 0 |n Frontiers in Pharmacology, Vol 13 (2022) 
787 0 |n https://www.frontiersin.org/articles/10.3389/fphar.2022.843110/full 
787 0 |n https://doaj.org/toc/1663-9812 
856 4 1 |u https://doaj.org/article/a9b43e6a4e6e486fa65e76909082b2f9  |z Connect to this object online.