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Abstract

Volume 20, Issue 6 (November 2018) 20, 561–566; 10.4103/aja.aja_57_18

Prognostic role of chromogranin A in castration-resistant prostate cancer: A meta-analysis

Peng Hong, Run-Qi Guo, Gang Song, Kai-Wei Yang, Lei Zhang, Xue-Song Li, Kai Zhang, Li-Qun Zhou

Department of Urology, Peking University First Hospital and Institute of Urology, National Research Centre for Genitourinary Oncology, Beijing 100034, China

Correspondence: Dr. LQ Zhou (zhoulqmail@sina.com) or Dr. XS Li (pineneedle@sina.com)

Date of Submission 14-Jan-2018 Date of Acceptance 01-Jun-2018 Date of Web Publication 31-Jul-2018

Abstract

We aimed to investigate the prognostic value of chromogranin A (CgA) in castration-resistant prostate cancer (CRPC). We conducted a systematic literature search of PubMed, Web of Science, and EMBASE for citations published prior to September 2017 that described CgA and CRPC and performed a standard meta-analysis on survival outcomes. Our meta-analysis included eight eligible studies with 686 patients. The results were as follows: progression-free survival (PFS) was associated with CgA level (hazard ratio [HR] = 2.47, 95% confidence interval [CI]: 1.47–4.14, P = 0.0006); PFS was relative to CgA change (HR = 9.22, 95% CI: 3.03–28.05, P < 0.0001); and overall survival (OS) was relative to CgA level (HR = 1.47, 95% CI: 1.15–1.87, P = 0.002). When we divided the patients into two groups according to therapy status, the result for OS relative to CgA level was an HR of 1.26 (95% CI: 1.09–1.45, P = 0.001) in the first-line hormonal therapy group, and an HR of 2.33 (95% CI: 1.40–3.89, P = 0.001) in the second-line hormonal therapy or chemotherapy group. This meta-analysis indicated that a high CgA level had a negative influence on OS and PFS in CRPC patients. In addition, CRPC patients with a rising CgA had a shorter PFS. Further studies are needed to verify the prognostic value of CgA in CRPC.

Keywords: castration-resistant prostate cancer; chromogranin A; prognosis

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Asian Journal of Andrology CN 31-1795/R ISSN 1008-682X  Copyright © 2023  Shanghai Materia Medica, Chinese Academy of Sciences.  All rights reserved.