Sipuleucel-T and androgen receptor-directed therapy for castration-resistant prostate cancer: A meta-analysis

3Citations
Citations of this article
44Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

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).

Cite

CITATION STYLE

APA

Yi, R., Chen, B., Duan, P., Zheng, C., Shen, H., Liu, Q., … Zhou, Z. (2016). Sipuleucel-T and androgen receptor-directed therapy for castration-resistant prostate cancer: A meta-analysis. Journal of Immunology Research. Hindawi Publishing Corporation. https://doi.org/10.1155/2016/4543861

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free