Cargando…

Sipuleucel-T and Androgen Receptor-Directed Therapy for Castration-Resistant Prostate Cancer: A Meta-Analysis

New treatments, such as sipuleucel-T and androgen receptor- (AR-) directed therapies (enzalutamide (Enz) and abiraterone acetate (AA)), have emerged and been approved for the management of castration-resistant prostate cancer (CRPC). There are still debates over their efficacy and clinical benefits....

Descripción completa

Detalles Bibliográficos
Autores principales: Yi, Renliang, Chen, Baoxin, Duan, Peng, Zheng, Chanjiao, Shen, Huanyu, Liu, Qun, Yuan, Chen, Ou, Weilin, Zhou, Zhiheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5183769/
https://www.ncbi.nlm.nih.gov/pubmed/28058266
http://dx.doi.org/10.1155/2016/4543861
_version_ 1782486112712785920
author Yi, Renliang
Chen, Baoxin
Duan, Peng
Zheng, Chanjiao
Shen, Huanyu
Liu, Qun
Yuan, Chen
Ou, Weilin
Zhou, Zhiheng
author_facet Yi, Renliang
Chen, Baoxin
Duan, Peng
Zheng, Chanjiao
Shen, Huanyu
Liu, Qun
Yuan, Chen
Ou, Weilin
Zhou, Zhiheng
author_sort Yi, Renliang
collection PubMed
description New treatments, such as sipuleucel-T and androgen receptor- (AR-) directed therapies (enzalutamide (Enz) and abiraterone acetate (AA)), have emerged and been approved for the management of castration-resistant prostate cancer (CRPC). There are still debates over their efficacy and clinical benefits. This meta-analysis aimed to investigate the efficacy and safety of sipuleucel-T and AR-directed therapies in patients with CRPC. RevMan 5.1 was used for pooled analysis and analysis of publication bias. Seven studies were included in the meta-analysis, with three studies in sipuleucel-T (totally 737 patients, 488 patients in treatment group, and 249 patients in placebo group) and four in AR-directed therapies (totally 5,199 patients, 3,015 patients in treatment group, and 2,184 patients in placebo group). Treatment with sipuleucel-T significantly improved overall survival in patients with CRPC and was not associated with increased risk of adverse event of grade ≥3 (p > 0.05). However, treatment with sipuleucel-T did not improve time-to-progression and reduction of prostate-specific antigen (PSA) level ≥50% was not significantly different from that with placebo. AR-directed therapies significantly improved overall survival in patients with CRPC and improved time-to-progression and reduction of PSA level ≥50%. AR-directed therapies did not increase risk of adverse event of grade ≥3 (p > 0.05).
format Online
Article
Text
id pubmed-5183769
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Hindawi Publishing Corporation
record_format MEDLINE/PubMed
spelling pubmed-51837692017-01-05 Sipuleucel-T and Androgen Receptor-Directed Therapy for Castration-Resistant Prostate Cancer: A Meta-Analysis Yi, Renliang Chen, Baoxin Duan, Peng Zheng, Chanjiao Shen, Huanyu Liu, Qun Yuan, Chen Ou, Weilin Zhou, Zhiheng J Immunol Res Review Article New treatments, such as sipuleucel-T and androgen receptor- (AR-) directed therapies (enzalutamide (Enz) and abiraterone acetate (AA)), have emerged and been approved for the management of castration-resistant prostate cancer (CRPC). There are still debates over their efficacy and clinical benefits. This meta-analysis aimed to investigate the efficacy and safety of sipuleucel-T and AR-directed therapies in patients with CRPC. RevMan 5.1 was used for pooled analysis and analysis of publication bias. Seven studies were included in the meta-analysis, with three studies in sipuleucel-T (totally 737 patients, 488 patients in treatment group, and 249 patients in placebo group) and four in AR-directed therapies (totally 5,199 patients, 3,015 patients in treatment group, and 2,184 patients in placebo group). Treatment with sipuleucel-T significantly improved overall survival in patients with CRPC and was not associated with increased risk of adverse event of grade ≥3 (p > 0.05). However, treatment with sipuleucel-T did not improve time-to-progression and reduction of prostate-specific antigen (PSA) level ≥50% was not significantly different from that with placebo. AR-directed therapies significantly improved overall survival in patients with CRPC and improved time-to-progression and reduction of PSA level ≥50%. AR-directed therapies did not increase risk of adverse event of grade ≥3 (p > 0.05). Hindawi Publishing Corporation 2016 2016-12-12 /pmc/articles/PMC5183769/ /pubmed/28058266 http://dx.doi.org/10.1155/2016/4543861 Text en Copyright © 2016 Renliang Yi et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Yi, Renliang
Chen, Baoxin
Duan, Peng
Zheng, Chanjiao
Shen, Huanyu
Liu, Qun
Yuan, Chen
Ou, Weilin
Zhou, Zhiheng
Sipuleucel-T and Androgen Receptor-Directed Therapy for Castration-Resistant Prostate Cancer: A Meta-Analysis
title Sipuleucel-T and Androgen Receptor-Directed Therapy for Castration-Resistant Prostate Cancer: A Meta-Analysis
title_full Sipuleucel-T and Androgen Receptor-Directed Therapy for Castration-Resistant Prostate Cancer: A Meta-Analysis
title_fullStr Sipuleucel-T and Androgen Receptor-Directed Therapy for Castration-Resistant Prostate Cancer: A Meta-Analysis
title_full_unstemmed Sipuleucel-T and Androgen Receptor-Directed Therapy for Castration-Resistant Prostate Cancer: A Meta-Analysis
title_short Sipuleucel-T and Androgen Receptor-Directed Therapy for Castration-Resistant Prostate Cancer: A Meta-Analysis
title_sort sipuleucel-t and androgen receptor-directed therapy for castration-resistant prostate cancer: a meta-analysis
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5183769/
https://www.ncbi.nlm.nih.gov/pubmed/28058266
http://dx.doi.org/10.1155/2016/4543861
work_keys_str_mv AT yirenliang sipuleuceltandandrogenreceptordirectedtherapyforcastrationresistantprostatecancerametaanalysis
AT chenbaoxin sipuleuceltandandrogenreceptordirectedtherapyforcastrationresistantprostatecancerametaanalysis
AT duanpeng sipuleuceltandandrogenreceptordirectedtherapyforcastrationresistantprostatecancerametaanalysis
AT zhengchanjiao sipuleuceltandandrogenreceptordirectedtherapyforcastrationresistantprostatecancerametaanalysis
AT shenhuanyu sipuleuceltandandrogenreceptordirectedtherapyforcastrationresistantprostatecancerametaanalysis
AT liuqun sipuleuceltandandrogenreceptordirectedtherapyforcastrationresistantprostatecancerametaanalysis
AT yuanchen sipuleuceltandandrogenreceptordirectedtherapyforcastrationresistantprostatecancerametaanalysis
AT ouweilin sipuleuceltandandrogenreceptordirectedtherapyforcastrationresistantprostatecancerametaanalysis
AT zhouzhiheng sipuleuceltandandrogenreceptordirectedtherapyforcastrationresistantprostatecancerametaanalysis