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Matching-adjusted indirect comparison of enzalutamide versus darolutamide doublet in mHSPC.

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Future oncology (London, England) 📖 저널 OA 90.9% 2021: 0/1 OA 2022: 1/2 OA 2023: 0/2 OA 2024: 3/4 OA 2025: 67/67 OA 2026: 79/88 OA 2021~2026 2025 Vol.21(19) p. 2459-2469
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유사 논문
P · Population 대상 환자/모집단
환자: metastatic hormone-sensitive prostate cancer (mHSPC) using a matching-adjusted indirect comparison (MAIC)
I · Intervention 중재 / 시술
추출되지 않음
C · Comparison 대조 / 비교
추출되지 않음
O · Outcome 결과 / 결론
[CONCLUSIONS] Enzalutamide + ADT showed better efficacy than darolutamide + ADT for treatment of patients with mHSPC. These findings can help inform treatment decisions in clinical practice.

Armstrong AJ, Pandya BJ, Bhadauria HS, Ganguli A, Daki V, Moura A, Azad AA

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[AIMS] To compare the efficacy of enzalutamide + androgen-deprivation therapy (ADT) versus darolutamide + ADT for treatment of patients with metastatic hormone-sensitive prostate cancer (mHSPC) using

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APA Armstrong AJ, Pandya BJ, et al. (2025). Matching-adjusted indirect comparison of enzalutamide versus darolutamide doublet in mHSPC.. Future oncology (London, England), 21(19), 2459-2469. https://doi.org/10.1080/14796694.2025.2526324
MLA Armstrong AJ, et al.. "Matching-adjusted indirect comparison of enzalutamide versus darolutamide doublet in mHSPC.." Future oncology (London, England), vol. 21, no. 19, 2025, pp. 2459-2469.
PMID 40654300 ↗

Abstract

[AIMS] To compare the efficacy of enzalutamide + androgen-deprivation therapy (ADT) versus darolutamide + ADT for treatment of patients with metastatic hormone-sensitive prostate cancer (mHSPC) using a matching-adjusted indirect comparison (MAIC).

[PATIENTS AND METHODS] Individual patient data from ARCHES (NCT02677896; enzalutamide + ADT,  = 1150) were weighted and adjusted to match published aggregated data on baseline characteristics from ARANOTE (NCT04736199; darolutamide + ADT,  = 669). The MAIC was anchored on the common comparator, placebo + ADT, and provided a (matching-adjusted) hazard ratio (HR) of enzalutamide versus darolutamide.

[RESULTS] Treatment with enzalutamide + ADT significantly prolonged the primary endpoint of radiographic progression-free survival (HR [95% confidence interval, CI]: 0.54 [0.32-0.93],  = 0.03) and time to castration resistance (HR [95% CI]: 0.57 [0.34-0.94],  = 0.03) compared with darolutamide + ADT (effective sample size: 319). Time to prostate-specific antigen progression (HR [95% CI]: 0.61 [0.29-1.30],  = 0.20) and time to initiation of new antineoplastic therapy (HR [95% CI]: 0.65 [0.34-1.24],  = 0.19) favored enzalutamide over darolutamide, albeit the difference was not statistically significant.

[CONCLUSIONS] Enzalutamide + ADT showed better efficacy than darolutamide + ADT for treatment of patients with mHSPC. These findings can help inform treatment decisions in clinical practice.

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