Assessment of androgen receptor signaling inhibitors therapy in metastatic hormone-sensitive prostate cancer

Androgen receptor signaling inhibitor (ARSI) therapy plays an important role in treating advanced prostate cancer. However, in Thailand, the efficacy and safety data of ARSI therapy remain limited. This study aimed to assess the efficacy and safety of ARSI therapy to treat patients with metastatic c...

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Main Authors: Jukapun Yoodee (Author), Chiraphon Detma (Author), Onuma Lappanawan (Author), Worachaya Pengthina (Author)
Format: Book
Published: Faculty of Pharmacy, Mahidol University, 2022-11-01T00:00:00Z.
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042 |a dc 
100 1 0 |a Jukapun Yoodee  |e author 
700 1 0 |a Chiraphon Detma  |e author 
700 1 0 |a Onuma Lappanawan  |e author 
700 1 0 |a Worachaya Pengthina  |e author 
245 0 0 |a Assessment of androgen receptor signaling inhibitors therapy in metastatic hormone-sensitive prostate cancer 
260 |b Faculty of Pharmacy, Mahidol University,   |c 2022-11-01T00:00:00Z. 
500 |a 10.29090/psa.2022.06.22.236 
500 |a 2586-8470 
520 |a Androgen receptor signaling inhibitor (ARSI) therapy plays an important role in treating advanced prostate cancer. However, in Thailand, the efficacy and safety data of ARSI therapy remain limited. This study aimed to assess the efficacy and safety of ARSI therapy to treat patients with metastatic castration na?ve prostate cancer. We collected data from electronic medical records based on disease progression and any reported adverse events. The primary outcome was progression-free survival (PFS) after initiating ARSI therapy. Secondary outcome was PFS according to abiraterone and enzalutamide, risk factors associated with PFS of ARSI therapy and adverse events. A total of 49 eligible patients were enrolled having received ARSI therapy (abiraterone or enzalutamide) to treat metastatic prostate cancer. The median time to follow-up was 17 months (interquartile range, 12-31). PFS among patients treated with ARSI therapy was 22 months (95% confidence interval [CI], 17-33), PFS among patients with abiraterone and enzalutamide was 21 and 23 months, respectively (hazard ratio [HR], 0.48; 95% CI, 0.17-1.41, P=0.185). Patients with Eastern Cooperative Group status 1-2 exhibited significantly decreased risk of disease progression (HR, 0.44; 95% CI, 0.20-0.96, P=0.038). The common adverse events included hypertension and fluid retention and edema. In conclusion, abiraterone and enzalutamide showed a trend to improve PFS among patients with metastatic castration naive prostate cancer. Adverse events were rarely reported, and patients were able to tolerate treatment. 
546 |a EN 
690 |a androgen receptor signaling inhibitor 
690 |a castration naive 
690 |a prostate cancer 
690 |a abiraterone 
690 |a enzalutamide 
690 |a Therapeutics. Pharmacology 
690 |a RM1-950 
690 |a Pharmacy and materia medica 
690 |a RS1-441 
690 |a Pharmaceutical industry 
690 |a HD9665-9675 
655 7 |a article  |2 local 
786 0 |n Pharmaceutical Sciences Asia, Vol 49, Iss 6, Pp 543-549 (2022) 
787 0 |n https://pharmacy.mahidol.ac.th/journal/_files/2022-49-6_3.pdf 
787 0 |n https://doaj.org/toc/2586-8470 
856 4 1 |u https://doaj.org/article/8ea771b274bd432f84fb65f7a3a428c6  |z Connect to this object online.