Introduction: Androgen-receptor pathway inhibitors such as abiraterone and enzalutamide have demonstrated clinical benefit in patients with metastatic castration-resistant prostate cancer (mCRPC). The aim of this study was to conduct a meta-analysis of published real-world evidence studies comparing outcomes among patients treated with enzalutamide or abiraterone in the first-line setting.
Methods: We conducted a systematic literature review to identify eligible studies. Evaluated outcomes were: overall survival (OS), progression-free survival, prostate-specific antigen (PSA) progression-free survival, PSA response, all-grade adverse events, grade ≥3 adverse events, treatment discontinuation, and dose reduction. Each outcome's suitability for meta-analysis was evaluated by assessing whether there were sufficient data to make comparisons between studies, consistency between outcome definitions, and whether the studies adjusted for baseline patient characteristics. Outcomes deemed suitable for meta-analysis were analyzed using fixed-effect and random-effect models to obtain pooled-effect sizes. Sensitivity analyses were conducted to evaluate the robustness of conclusions.
Results: Of 1849 records reviewed, 30 were eligible for inclusion. Most outcomes were deemed unsuitable for meta-analysis due to a lack of adjustment for baseline characteristics, issues with inconsistent outcome definitions, and the small number of studies reporting each outcome. The only outcome deemed suitable for meta-analysis was OS. A total of 17 studies reported hazard ratios (HRs) for OS, 11 of which were adjusted for baseline characteristics. Among the studies reporting adjusted HRs, the pooled-effect estimate favored enzalutamide over abiraterone (reference group) in the fixed-effect model (HR: 0.90 [95% CI: 0.87-0.93]) and the random-effect model (HR: 0.90 [95% CI: 0.86-0.94]). These results were consistent across all sensitivity analyses.
Discussion: Across all analyses, enzalutamide demonstrated a statistically significant improvement in OS compared with abiraterone. These findings highlight the value of real-world evidence studies to demonstrate the potential of different therapies under real-world conditions and over long periods of time.
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http://dx.doi.org/10.3389/fonc.2025.1491314 | DOI Listing |
Clin Cancer Res
March 2025
Cedars-Sinai Medical Center, Los Angeles, California, United States.
Background: Circulating tumor cells (CTCs) with a very-small-nuclear phenotype (vsnCTCs) in prostate cancer (PCa) are characterized by nuclei smaller than 8.5 μm. Our previous studies established an association between vsnCTCs and visceral metastasis.
View Article and Find Full Text PDFCrit Rev Oncol Hematol
March 2025
Medical Oncology Department, Hospital Universitario 12 de Octubre, Madrid, Spain.
The treatment of metastatic castration-resistant prostate cancer (mCRPC) has been rapidly evolving over the last two decades. The advent of new androgen receptor pathway inhibitors (ARPIs) such as abiraterone acetate or enzalutamide marks a great advance for treating mCRPC patientd in the pre- and post-docetaxel settings. The subsequent approval of ARPIs in early stages-i.
View Article and Find Full Text PDFFuture Oncol
March 2025
Urology San Antonio, San Antonio, TX, USA.
Relugolix is a once-daily oral gonadotropin-releasing hormone antagonist that was approved by the U.S. Food and Drug Administration in 2020 for the treatment of advanced prostate cancer.
View Article and Find Full Text PDFFront Oncol
February 2025
Department of Urology, Affiliated Hospital of North Sichuan Medical College, Nanchong, Sichuan, China.
Purpose: This study aims to retrospectively describe the perioperative outcomes and short-term oncological outcomes of high-risk prostate cancer patients treated with neoadjuvant novel hormonal therapy (NNHT) combined with radical prostatectomy (RP) or RP alone.
Materials And Methods: Fifty-five male patients underwent RP and were categorized based on whether NNHT was administered preoperatively. Clinical baseline characteristics, perioperative outcomes, and biochemical recurrence (BCR) rate were summarized using mean, standard deviation, medians, interquartile ranges, and frequencies.
Future Oncol
March 2025
Value & Evidence, EVERSANA™, Burlington, ON, Canada.
Aims: The absence of direct comparisons between talazoparib plus enzalutamide (TALA+ENZA) and current standard of care hinders evaluating their relative efficacy for first-line (1 L) metastatic castration resistant prostate cancer (mCRPC). This study aimed to compare TALA+ENZA (TALAPRO-2) to abiraterone acetate plus prednisone (AAP) (COU-AA-302) and docetaxel (TAX 327) using a matching-adjusted indirect treatment comparison (MAIC).
Methods: A systematic literature review using the Ovid® interface was performed to identify relevant evidence.
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