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Androgen receptor axis-targeted agents are not superior to conventional hormonal therapy for treatment of metastatic prostate cancer.

Authors :
Wada, Akinori
Narita, Mitsuhiro
Nagasawa, Masayuki
Kusaba, Takuto
Kubota, Shigehisa
Yoshida, Tetsuya
Johnin, Kazuyoshi
Kawauchi, Akihiro
Kageyama, Susumu
Source :
Oncology Letters; Oct2022, Vol. 24 Issue 4, pN.PAG-N.PAG, 1p
Publication Year :
2022

Abstract

The present study aimed to use real-world Japanese data to compare the treatment outcome of conventional hormonal therapy to that of using androgen receptor axis-targeted (ARAT) agents for patients with metastatic castration-resistant prostate cancer. The overall survival between the conventional hormonal therapy group and the ARAT agent therapy group was compared using a group of 75 Japanese patients who were treated for metastatic castration-resistant prostate cancer. A subgroup analysis was carried out and the risk factors that affected overall survival (OS) were determined. The median OS from the time of prostate-specific antigen recurrence was 73.1 months in the ARAT group and 45.2 months in the conventional treatment group (P=0.414). Although OS tended to be slightly longer in the ARAT group, the difference between the groups was not significant. Subgroup analysis suggested that the therapeutic outcome of using ARAT agents tended to be less beneficial in patients who were older, and in those with a higher tumor volume or low Gleason grade. In conclusion, use of ARAT agents did not impart a significant survival benefit to patients with metastatic castration-resistant prostate cancer when compared with survival rates in response to conventional therapy. However, there was some clinical benefit when ARAT agents were used after patients developed castration-resistant prostate cancer. These findings suggest that up-front therapy using ARAT agents at the time of the initial hormone therapy can impart clinical benefit in Japanese patients with metastatic prostate cancer. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
17921074
Volume :
24
Issue :
4
Database :
Complementary Index
Journal :
Oncology Letters
Publication Type :
Academic Journal
Accession number :
159266730
Full Text :
https://doi.org/10.3892/ol.2022.13453