Trends in the Use of Second-Generation Androgen Receptor Axis Inhibitors for Metastatic Hormone-Sensitive Prostate Cancer and Clinical Factors Predicting Biological Recurrence

Author:

Nakane Keita1ORCID,Watanabe Hiromitsu2,Naiki Taku3ORCID,Takahara Kiyoshi4ORCID,Yasui Takahiro3ORCID,Miyake Hideaki2,Shiroki Ryoichi4,Koie Takuya1ORCID

Affiliation:

1. Department of Urology, Gifu University Graduate School of Medicine, Gifu 5011194, Japan

2. Department of Urology, Hamamatsu University School of Medicine, Hamamatsu 4313192, Japan

3. Department of Nephro-urology, Graduate School of Medical Sciences, Nagoya City University, Nagoya 4678601, Japan

4. Department of Urology, Fujita Health University School of Medicine, Toyoake 4701192, Japan

Abstract

The advent of second-generation androgen receptor axis-targeted agents (ARATs) has revolutionized the treatment of metastatic hormone-sensitive prostate cancer (mHSPC). Biochemical recurrence-free survival (BRFS) was used to compare the efficacy of each ARAT. This multicenter retrospective study included 581 patients with newly diagnosed mHSPC who received first-line hormone therapy. The characteristics of patients treated with different ARATs were compared as well as changes in the usage of each drug over time. For BRFS, the apalutamide (Apa) and enzalutamide (Enza) groups, as well as the abiraterone acetate (Abi) and Apa/Enza groups, were compared. In addition, multivariate analysis was performed to determine predictive factors for biochemical recurrence (BCR). The use of second-generation ARATs tended to increase after May 2020. No significant difference in BRFS was found between patients receiving Apa and Enza (p = 0.490) and those receiving Abi or Apa/Enza (p = 0.906). Multivariate analysis revealed that the neutrophil-to-lymphocyte ratio (NLR) ≥ 2.76 and PSA ≥ 0.550 ng/mL were independent predictors of BCR. There were no significant differences in patient characteristics or BRFS in patients with mHSPC receiving different ARATs as first-line treatment. NLR and PSA may be prognostic factors following the first-line treatment of patients with mHSPC.

Publisher

MDPI AG

Subject

Clinical Biochemistry

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