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Comparing efficacy of first-line treatment of metastatic castration resistant prostate cancer: a network meta-analysis of randomized controlled trials.
Liu, Yang; Deng, Xianzhong; Wen, Zhi; Huang, Jing; Wang, Chongjian; Chen, Caixia; Bao, Erhao; Wang, Jiahao; Yang, Xuesong.
Affiliation
  • Liu Y; Department of Urology, Affiliated Hospital of North Sichuan Medical College, Nanchong, China.
  • Deng X; Department of Urology, Chengdu Xinhua Hospital Affiliated to North Sichuan Medical College, Chengdu, China.
  • Wen Z; Department of Urology, Affiliated Hospital of North Sichuan Medical College, Nanchong, China.
  • Huang J; Department of Urology, Affiliated Hospital of North Sichuan Medical College, Nanchong, China.
  • Wang C; Department of Urology, Affiliated Hospital of North Sichuan Medical College, Nanchong, China.
  • Chen C; Department of Urology, Affiliated Hospital of North Sichuan Medical College, Nanchong, China.
  • Bao E; Department of Urology, Affiliated Hospital of North Sichuan Medical College, Nanchong, China.
  • Wang J; Department of Urology, Affiliated Hospital of North Sichuan Medical College, Nanchong, China.
  • Yang X; Department of Urology, Affiliated Hospital of North Sichuan Medical College, Nanchong, China.
Front Pharmacol ; 14: 1290990, 2023.
Article in En | MEDLINE | ID: mdl-38074136
Background: Metastatic castration-resistant prostate cancer (mCRPC) presents significant treatment selection challenges due to limited therapeutic options. This study aimed to comprehensively assess the efficacy of multiple treatment regimens for mCRPC through a network meta-analysis (NMA) of randomized controlled trials (RCTs). Methods: A systematically comprehensive search for randomized controlled trials (RCTs) was performed in Pubmed, Cochrane Library, Embase, and Web of Science databases. The network meta-analysis was employed to compare the overall survival (OS), progression-free survival (PFS), and radiographic progression-free survival (rPFS) among different interventions at specific time points. This study was prospectively registered with PROSPERO (CRD42023422823). Results: A total of 29 RCTs, involving 12,706 patients and investigating 16 interventions, were included in the analysis. Chempretarget ((capivasertib or cabozantinib) + docetaxel + prednisone)) and PARP (Olaparib or rucaparib) inhibitors emerged as interventions that significantly improved survival outcomes compared to first-line treatment in mCRPC patients. Chempretarget demonstrated superior overall survival starting from the 12th month, while PARP inhibitors showed a clear advantage in progression-free survival within the 3-18 months range. Notably, chempre ((Docetaxel or Cabazitaxel) + prednisone) exhibited favorable performance in radiographic progression-free survival during the 3-18 month period. Conclusion: Our findings underscore the efficacy of chempretarget, PARP inhibitors, and chempre in enhancing survival outcomes for mCRPC patients. Further head-to-head comparisons are warranted to validate these results. These findings carry important implications for treatment decision-making in mCRPC and may guide the development of more effective therapeutic strategies.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Systematic_reviews Language: En Journal: Front Pharmacol Year: 2023 Document type: Article Affiliation country: China Country of publication: Switzerland

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Systematic_reviews Language: En Journal: Front Pharmacol Year: 2023 Document type: Article Affiliation country: China Country of publication: Switzerland