Efficacy of Combination Therapy With Radium-223 and Enzalutamide in Castration-resistant Prostate Cancer With Bone Metastases.


Journal

Anticancer research
ISSN: 1791-7530
Titre abrégé: Anticancer Res
Pays: Greece
ID NLM: 8102988

Informations de publication

Date de publication:
Jun 2024
Historique:
received: 02 04 2024
revised: 18 04 2024
accepted: 19 04 2024
medline: 1 6 2024
pubmed: 1 6 2024
entrez: 31 5 2024
Statut: ppublish

Résumé

Radium-223 therapy has been reported to improve prognosis in patients with castration-resistant prostate cancer (CRPC) and bone metastases. Occasionally, radium-223 and androgen receptor signaling inhibitors (ARSIs) are used in combination for disease control, but the efficacy of this combination is unclear. This study assessed the efficacy of the addition of enzalutamide in patients treated with radium-223. We included patients with CRPC and bone metastases who were treated with radium-223 at our institution. Patients were assigned to the enzalutamide combination group or non-combination group. We compared progression-free survival (PFS), overall survival (OS), and the completion rate of radium-223 between the two groups. In total, 39 patients with CRPC were included in this retrospective study. The median follow-up duration was 8.8 months. The enzalutamide combination and non-combination groups included 22 (56.4%) and 17 patients (43.6%), respectively. Median PFS was 11.3 months [95% confidence interval (CI)=3.9-19.9] in the combination group, versus 3.0 months (95%CI=1.9-5.5) in the non-combination group (p=0.004). Median OS did not significantly differ between the groups. The radium-223 completion rate was higher in the combination group than in the non-combination group (72.7% vs. 35.3%, p=0.026). The combined use of enzalutamide with radium-223 therapy improved PFS and treatment completion rates in patients with CRPC and bone metastases. This combination may be associated with a more favorable prognosis.

Sections du résumé

BACKGROUND/AIM OBJECTIVE
Radium-223 therapy has been reported to improve prognosis in patients with castration-resistant prostate cancer (CRPC) and bone metastases. Occasionally, radium-223 and androgen receptor signaling inhibitors (ARSIs) are used in combination for disease control, but the efficacy of this combination is unclear. This study assessed the efficacy of the addition of enzalutamide in patients treated with radium-223.
PATIENTS AND METHODS METHODS
We included patients with CRPC and bone metastases who were treated with radium-223 at our institution. Patients were assigned to the enzalutamide combination group or non-combination group. We compared progression-free survival (PFS), overall survival (OS), and the completion rate of radium-223 between the two groups.
RESULTS RESULTS
In total, 39 patients with CRPC were included in this retrospective study. The median follow-up duration was 8.8 months. The enzalutamide combination and non-combination groups included 22 (56.4%) and 17 patients (43.6%), respectively. Median PFS was 11.3 months [95% confidence interval (CI)=3.9-19.9] in the combination group, versus 3.0 months (95%CI=1.9-5.5) in the non-combination group (p=0.004). Median OS did not significantly differ between the groups. The radium-223 completion rate was higher in the combination group than in the non-combination group (72.7% vs. 35.3%, p=0.026).
CONCLUSION CONCLUSIONS
The combined use of enzalutamide with radium-223 therapy improved PFS and treatment completion rates in patients with CRPC and bone metastases. This combination may be associated with a more favorable prognosis.

Identifiants

pubmed: 38821616
pii: 44/6/2627
doi: 10.21873/anticanres.17069
doi:

Substances chimiques

Phenylthiohydantoin 2010-15-3
Benzamides 0
enzalutamide 93T0T9GKNU
Nitriles 0
Radium W90AYD6R3Q
Radium-223 8BR2SOL3L1

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

2627-2635

Informations de copyright

Copyright © 2024 International Institute of Anticancer Research (Dr. George J. Delinasios), All rights reserved.

Auteurs

Naoto Wakita (N)

Department of Urology, Kobe University Graduate School of Medicine, Kobe, Japan complus_duefl@yahoo.co.jp.

Takuto Hara (T)

Department of Urology, Kobe University Graduate School of Medicine, Kobe, Japan.

Kotaro Suzuki (K)

Department of Urology, Kobe University Graduate School of Medicine, Kobe, Japan.

Tomoaki Terakawa (T)

Department of Urology, Kobe University Graduate School of Medicine, Kobe, Japan.

Jun Teishima (J)

Department of Urology, Kobe University Graduate School of Medicine, Kobe, Japan.

Yuzo Nakano (Y)

Department of Urology, Kobe University Graduate School of Medicine, Kobe, Japan.

Hideaki Miyake (H)

Department of Urology, Kobe University Graduate School of Medicine, Kobe, Japan.

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Classifications MeSH