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A multicenter phase I/II study of enzalutamide in Japanese patients with castration-resistant prostate cancer
BACKGROUND: The safety, tolerability, pharmacokinetics (PK) and anti-tumor activity of enzalutamide were investigated in patients with castration-resistant prostate cancer (CRPC) in Japan through a multicenter phase I/II study. METHODS: In phase I, patients with progressive metastatic CRPC received...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Springer Japan
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4967591/ https://www.ncbi.nlm.nih.gov/pubmed/26793974 http://dx.doi.org/10.1007/s10147-016-0952-6 |
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author | Akaza, Hideyuki Uemura, Hirotsugu Tsukamoto, Taiji Ozono, Seiichiro Ogawa, Osamu Sakai, Hideki Oya, Mototsugu Namiki, Mikio Fukasawa, Satoshi Yamaguchi, Akito Uemura, Hiroji Ohashi, Yasuo Maeda, Hideki Saito, Atsushi Takeda, Kentaro Naito, Seiji |
author_facet | Akaza, Hideyuki Uemura, Hirotsugu Tsukamoto, Taiji Ozono, Seiichiro Ogawa, Osamu Sakai, Hideki Oya, Mototsugu Namiki, Mikio Fukasawa, Satoshi Yamaguchi, Akito Uemura, Hiroji Ohashi, Yasuo Maeda, Hideki Saito, Atsushi Takeda, Kentaro Naito, Seiji |
author_sort | Akaza, Hideyuki |
collection | PubMed |
description | BACKGROUND: The safety, tolerability, pharmacokinetics (PK) and anti-tumor activity of enzalutamide were investigated in patients with castration-resistant prostate cancer (CRPC) in Japan through a multicenter phase I/II study. METHODS: In phase I, patients with progressive metastatic CRPC received single, then multiple, ascending doses of enzalutamide 80, 160 or 240 mg/day. After assessment of tolerability at multiple doses of 160 mg/day for 4 weeks, post-docetaxel patients with CRPC and measurable disease were enrolled into phase II; receiving long-term administration of enzalutamide 160 mg/day. RESULTS: Nine and 38 patients were enrolled in phase I and II, respectively. During phase I, enzalutamide was well tolerated in each cohort; PK parameters were similar to those of non-Japanese populations in other studies. By week 12, overall response rate was 5.3 % and clinical benefit rate was 47.4 %. Prostate-specific antigen response rate (≥50 % reduction from baseline) was 28.9 %. Treatment-emergent adverse events reported in >20 % of patients in phase II were decreased weight, decreased appetite and constipation. No seizures were observed. CONCLUSION: Enzalutamide at 160 mg/day was well tolerated, with PK and safety profiles similar to the non-Japanese population. Anti-tumor activity was observed in post-docetaxel Japanese patients with metastatic CRPC. Apparent differences in anti-tumor activity compared with the AFFIRM study (a phase III trial in a diverse population of patients with CRPC post-docetaxel) may be attributed to differences in treatment history prior to starting enzalutamide. Particularly in Japan, the influence of sequence in hormone treatments, including combined androgen blockade therapy, should be considered. Trial registration: ClinicalTrials.gov NCT01284920. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s10147-016-0952-6) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4967591 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Springer Japan |
record_format | MEDLINE/PubMed |
spelling | pubmed-49675912016-08-12 A multicenter phase I/II study of enzalutamide in Japanese patients with castration-resistant prostate cancer Akaza, Hideyuki Uemura, Hirotsugu Tsukamoto, Taiji Ozono, Seiichiro Ogawa, Osamu Sakai, Hideki Oya, Mototsugu Namiki, Mikio Fukasawa, Satoshi Yamaguchi, Akito Uemura, Hiroji Ohashi, Yasuo Maeda, Hideki Saito, Atsushi Takeda, Kentaro Naito, Seiji Int J Clin Oncol Original Article BACKGROUND: The safety, tolerability, pharmacokinetics (PK) and anti-tumor activity of enzalutamide were investigated in patients with castration-resistant prostate cancer (CRPC) in Japan through a multicenter phase I/II study. METHODS: In phase I, patients with progressive metastatic CRPC received single, then multiple, ascending doses of enzalutamide 80, 160 or 240 mg/day. After assessment of tolerability at multiple doses of 160 mg/day for 4 weeks, post-docetaxel patients with CRPC and measurable disease were enrolled into phase II; receiving long-term administration of enzalutamide 160 mg/day. RESULTS: Nine and 38 patients were enrolled in phase I and II, respectively. During phase I, enzalutamide was well tolerated in each cohort; PK parameters were similar to those of non-Japanese populations in other studies. By week 12, overall response rate was 5.3 % and clinical benefit rate was 47.4 %. Prostate-specific antigen response rate (≥50 % reduction from baseline) was 28.9 %. Treatment-emergent adverse events reported in >20 % of patients in phase II were decreased weight, decreased appetite and constipation. No seizures were observed. CONCLUSION: Enzalutamide at 160 mg/day was well tolerated, with PK and safety profiles similar to the non-Japanese population. Anti-tumor activity was observed in post-docetaxel Japanese patients with metastatic CRPC. Apparent differences in anti-tumor activity compared with the AFFIRM study (a phase III trial in a diverse population of patients with CRPC post-docetaxel) may be attributed to differences in treatment history prior to starting enzalutamide. Particularly in Japan, the influence of sequence in hormone treatments, including combined androgen blockade therapy, should be considered. Trial registration: ClinicalTrials.gov NCT01284920. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s10147-016-0952-6) contains supplementary material, which is available to authorized users. Springer Japan 2016-01-21 2016 /pmc/articles/PMC4967591/ /pubmed/26793974 http://dx.doi.org/10.1007/s10147-016-0952-6 Text en © The Author(s) 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Original Article Akaza, Hideyuki Uemura, Hirotsugu Tsukamoto, Taiji Ozono, Seiichiro Ogawa, Osamu Sakai, Hideki Oya, Mototsugu Namiki, Mikio Fukasawa, Satoshi Yamaguchi, Akito Uemura, Hiroji Ohashi, Yasuo Maeda, Hideki Saito, Atsushi Takeda, Kentaro Naito, Seiji A multicenter phase I/II study of enzalutamide in Japanese patients with castration-resistant prostate cancer |
title | A multicenter phase I/II study of enzalutamide in Japanese patients with castration-resistant prostate cancer |
title_full | A multicenter phase I/II study of enzalutamide in Japanese patients with castration-resistant prostate cancer |
title_fullStr | A multicenter phase I/II study of enzalutamide in Japanese patients with castration-resistant prostate cancer |
title_full_unstemmed | A multicenter phase I/II study of enzalutamide in Japanese patients with castration-resistant prostate cancer |
title_short | A multicenter phase I/II study of enzalutamide in Japanese patients with castration-resistant prostate cancer |
title_sort | multicenter phase i/ii study of enzalutamide in japanese patients with castration-resistant prostate cancer |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4967591/ https://www.ncbi.nlm.nih.gov/pubmed/26793974 http://dx.doi.org/10.1007/s10147-016-0952-6 |
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