Your browser doesn't support javascript.
loading
Survival outcome of chemotherapy-naïve castration-resistant prostate cancer treated with new-generation androgen receptor axis-targeted agents in real-world analysis.
Shimomura, Tatsuya; Mori, Keiichiro; Yasue, Keiji; Matsukawa, Akihiro; Fukuokaya, Wataru; Yanagisawa, Takafumi; Hata, Kenichi; Murakami, Masaya; Koike, Yusuke; Miki, Jun; Yamada, Hiroki; Kimura, Takahiro.
Affiliation
  • Shimomura T; Department of Urology, Jikei University School of Medicine, Tokyo, Japan. shimomura@jikei.ac.jp.
  • Mori K; Department of Urology, Jikei University School of Medicine, Tokyo, Japan.
  • Yasue K; Department of Urology, Jikei University School of Medicine, Tokyo, Japan.
  • Matsukawa A; Department of Urology, Jikei University School of Medicine, Tokyo, Japan.
  • Fukuokaya W; Department of Urology, Jikei University School of Medicine, Tokyo, Japan.
  • Yanagisawa T; Department of Urology, Jikei University School of Medicine, Tokyo, Japan.
  • Hata K; Department of Urology, Jikei University School of Medicine, Tokyo, Japan.
  • Murakami M; Department of Urology, Atsugi City General Hospital, Atsugi, Japan.
  • Koike Y; Department of Urology, Jikei University School of Medicine, Tokyo, Japan.
  • Miki J; Department of Urology, Fuji City General Hospital, Fuji, Japan.
  • Yamada H; Department of Urology, Jikei University School of Medicine, Tokyo, Japan.
  • Kimura T; Department of Urology, JR Tokyo General Hospital, Tokyo, Japan.
Int J Clin Oncol ; 29(2): 213-221, 2024 Feb.
Article in En | MEDLINE | ID: mdl-38103156
ABSTRACT

PURPOSE:

The androgen receptor axis-targeted (ARAT) agents abiraterone and enzalutamide have been introduced against castration-resistant prostate cancer (CRPC). However, determining which of these agents should be used first is a clinical challenge. Therefore, in this study, we compared the efficacy of first-line abiraterone and enzalutamide treatments in chemotherapy-naïve patients with CRPC.

METHODS:

A total of 242 chemotherapy-naïve CRPC cases treated with first-line ARAT were analyzed. Outcome measures were PSA response, PSA progression-free survival (PSA-PFS), time to treatment failure (TTF), cancer specific survival (CSS), and overall survival (OS).

RESULTS:

Abiraterone (A) and enzalutamide (E) were administered to 61 and 181 patients, respectively. The median PSA response rate (- 65.4% [A] and - 78.8% [E], p = 0.0341), PSA decline ≥ 30% (55.7% [A] and 72.9% [E], p = 0.0183), PSA-PFS (median 4 months [A] and 8 months [E], p = 0.0126), TTF (median 6 months [A] and 14 months [E], p < 0.0001), CSS (median 45 months [A] and not reached [E], p < 0.0001), and OS (median 28 months [A] and 80 months [E], p < 0.001) were significantly better in the enzalutamide group. In the multivariate analyses for CSS and OS, ALP (p = 0.00376) and ARAT (p < 0.001) (CSS), evidence of metastasis (p = 0.0467), Hb (p = 0.00205), and ARAT (p = 0.00514) (OS) were significant factors, respectively.

CONCLUSION:

This study showed that PSA response, PSA-PFS, TTF, CSS, and OS were better with first-line enzalutamide administration. Direct inhibition of androgen receptor signaling by enzalutamide is associated with better clinical outcomes.
Subject(s)
Key words

Full text: 1 Database: MEDLINE Main subject: Benzamides / Receptors, Androgen / Prostatic Neoplasms, Castration-Resistant Limits: Humans / Male Language: En Year: 2024 Type: Article

Full text: 1 Database: MEDLINE Main subject: Benzamides / Receptors, Androgen / Prostatic Neoplasms, Castration-Resistant Limits: Humans / Male Language: En Year: 2024 Type: Article