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Efficacy and safety of triple or dual therapies for metastatic hormone-sensitive prostate cancer: a systematic review and Bayesian network meta-analysis.

Future oncology (London, England) 2026 Vol.22(5) p. 567-582

Jiang J, Wang Y, Bai J, Yang G, Wang H, Ding H, Zhang Y, Zhai Z, Dong Z, Wang Z

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To compare triple and dual therapies for efficacy and safety in metastatic hormone-sensitive prostate cancer (mHSPC).

🔬 핵심 임상 통계 (초록에서 자동 추출 — 원문 검증 권장)
  • 95% CI 0.39-0.76
  • HR 0.33
  • 연구 설계 meta-analysis

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BibTeX ↓ RIS ↓
APA Jiang J, Wang Y, et al. (2026). Efficacy and safety of triple or dual therapies for metastatic hormone-sensitive prostate cancer: a systematic review and Bayesian network meta-analysis.. Future oncology (London, England), 22(5), 567-582. https://doi.org/10.2217/FON-2022-1114
MLA Jiang J, et al.. "Efficacy and safety of triple or dual therapies for metastatic hormone-sensitive prostate cancer: a systematic review and Bayesian network meta-analysis.." Future oncology (London, England), vol. 22, no. 5, 2026, pp. 567-582.
PMID 41697112

Abstract

To compare triple and dual therapies for efficacy and safety in metastatic hormone-sensitive prostate cancer (mHSPC). A Bayesian network meta-analysis was conducted to indirectly compare overall survival, progression-free survival and adverse events in mHSPC patients with triple and dual therapies. Triple and dual therapies were related to considerably higher overall survival than androgen-deprivation therapy (ADT), and darolutamide + docetaxel + ADT (hazard ratio [HR]: 0.54; 95% CI: 0.39-0.76; P score = 0.89) emerged as the best option. In terms of progression-free survival, abiraterone + prednisolone + docetaxel + ADT (HR: 0.33; 95% CI: 0.19-0.53; P score = 0.92) emerged as the best option. Apalutamide + ADT had the lowest odds of adverse events. Triple therapies were particularly effective in mHSPC patients, but the incidence of adverse events was significantly high.

MeSH Terms

Humans; Male; Bayes Theorem; Prostatic Neoplasms; Antineoplastic Combined Chemotherapy Protocols; Network Meta-Analysis as Topic; Treatment Outcome; Androgen Antagonists; Neoplasm Metastasis; Docetaxel; Androstenes; Thiohydantoins

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