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Prognostic impact of dose reduction in androgen receptor pathway inhibitors for castration-resistant prostate cancer
BACKGROUND: Androgen receptor pathway inhibitors (ARPIs) such as abiraterone and enzalutamide have been shown to prolong survival in patients with advanced prostate cancer. However, there is limited evidence on the anticancer effect of a reduced dose of ARPIs. This study compared the prognosis in pa...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Asian Pacific Prostate Society
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9042776/ https://www.ncbi.nlm.nih.gov/pubmed/35510101 http://dx.doi.org/10.1016/j.prnil.2021.10.001 |
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author | Yamada, Shigetomo Shiota, Masaki Blas, Leandro Matsumoto, Takashi Kashiwagi, Eiji Takeuchi, Ario Inokuchi, Junichi Shiga, Ken-ichiro Yokomizo, Akira Eto, Masatoshi |
author_facet | Yamada, Shigetomo Shiota, Masaki Blas, Leandro Matsumoto, Takashi Kashiwagi, Eiji Takeuchi, Ario Inokuchi, Junichi Shiga, Ken-ichiro Yokomizo, Akira Eto, Masatoshi |
author_sort | Yamada, Shigetomo |
collection | PubMed |
description | BACKGROUND: Androgen receptor pathway inhibitors (ARPIs) such as abiraterone and enzalutamide have been shown to prolong survival in patients with advanced prostate cancer. However, there is limited evidence on the anticancer effect of a reduced dose of ARPIs. This study compared the prognosis in patients with chemotherapy-naïve castration-resistant prostate cancer (CRPC) between ARPI treatment with standard dose and treatment with reduced dose. METHODS: Japanese patients who were treated with ARPI as first-line treatment for CRPC between 2014 and 2018 were included. The associations between dose reduction and clinicopathological factors, progression-free survival, and overall survival were investigated. RESULTS: Of the 162 patients included, 33 (20.4%) patients had their dose reduced during ARPI treatment. In the multivariate analysis, higher PSA, abiraterone treatment, and dose reduction were significant prognostic factors for progression-free survival (PFS); however, dose reduction was not associated with overall survival. In the enzalutamide-treated group, the median PFS was 12.1 months (95% CI, 8.5–21.4 months) in the standard-dose group and 7.2 months (95% CI, 5.0–11.5 months) in the reduced-dose group (P = 0.038). CONCLUSION: This study suggests inferior oncological outcome when treated with reduced-dose ARPI for CRPC. Full-dose administration of ARPI for CRPC may be appropriate if feasible. |
format | Online Article Text |
id | pubmed-9042776 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Asian Pacific Prostate Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-90427762022-05-03 Prognostic impact of dose reduction in androgen receptor pathway inhibitors for castration-resistant prostate cancer Yamada, Shigetomo Shiota, Masaki Blas, Leandro Matsumoto, Takashi Kashiwagi, Eiji Takeuchi, Ario Inokuchi, Junichi Shiga, Ken-ichiro Yokomizo, Akira Eto, Masatoshi Prostate Int Research Article BACKGROUND: Androgen receptor pathway inhibitors (ARPIs) such as abiraterone and enzalutamide have been shown to prolong survival in patients with advanced prostate cancer. However, there is limited evidence on the anticancer effect of a reduced dose of ARPIs. This study compared the prognosis in patients with chemotherapy-naïve castration-resistant prostate cancer (CRPC) between ARPI treatment with standard dose and treatment with reduced dose. METHODS: Japanese patients who were treated with ARPI as first-line treatment for CRPC between 2014 and 2018 were included. The associations between dose reduction and clinicopathological factors, progression-free survival, and overall survival were investigated. RESULTS: Of the 162 patients included, 33 (20.4%) patients had their dose reduced during ARPI treatment. In the multivariate analysis, higher PSA, abiraterone treatment, and dose reduction were significant prognostic factors for progression-free survival (PFS); however, dose reduction was not associated with overall survival. In the enzalutamide-treated group, the median PFS was 12.1 months (95% CI, 8.5–21.4 months) in the standard-dose group and 7.2 months (95% CI, 5.0–11.5 months) in the reduced-dose group (P = 0.038). CONCLUSION: This study suggests inferior oncological outcome when treated with reduced-dose ARPI for CRPC. Full-dose administration of ARPI for CRPC may be appropriate if feasible. Asian Pacific Prostate Society 2022-03 2021-10-30 /pmc/articles/PMC9042776/ /pubmed/35510101 http://dx.doi.org/10.1016/j.prnil.2021.10.001 Text en © 2022 Asian Pacific Prostate Society. Publishing services by Elsevier B.V. https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Research Article Yamada, Shigetomo Shiota, Masaki Blas, Leandro Matsumoto, Takashi Kashiwagi, Eiji Takeuchi, Ario Inokuchi, Junichi Shiga, Ken-ichiro Yokomizo, Akira Eto, Masatoshi Prognostic impact of dose reduction in androgen receptor pathway inhibitors for castration-resistant prostate cancer |
title | Prognostic impact of dose reduction in androgen receptor pathway inhibitors for castration-resistant prostate cancer |
title_full | Prognostic impact of dose reduction in androgen receptor pathway inhibitors for castration-resistant prostate cancer |
title_fullStr | Prognostic impact of dose reduction in androgen receptor pathway inhibitors for castration-resistant prostate cancer |
title_full_unstemmed | Prognostic impact of dose reduction in androgen receptor pathway inhibitors for castration-resistant prostate cancer |
title_short | Prognostic impact of dose reduction in androgen receptor pathway inhibitors for castration-resistant prostate cancer |
title_sort | prognostic impact of dose reduction in androgen receptor pathway inhibitors for castration-resistant prostate cancer |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9042776/ https://www.ncbi.nlm.nih.gov/pubmed/35510101 http://dx.doi.org/10.1016/j.prnil.2021.10.001 |
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