Prognostic value of serum alkaline phosphatase in the survival of prostate cancer: evidence from a meta-analysis

• Published in: Cancer management and research Vol. 10; pp. 3125 - 3139
• Main Authors: Li, Dongyang, Lv, Hang, Hao, Xuanyu, Hu, Bin, Song, Yongsheng
• Format: Journal Article
• Language: English
• Published: New Zealand Dove Medical Press Limited 01.01.2018; Taylor & Francis Ltd; Dove Medical Press
• Subjects: Alkaline phosphatase; Antigens; Biomarkers; Cancer therapies; Chemotherapy; Hemoglobin; Medical prognosis; Medical research; Meta-analysis; Metastasis; Online databases; Original Research; Patient outcomes; Phosphatase; Phosphatases; Prognosis; Prostate cancer; Quality; Studies; survival; Urology; United States > US; China; meta-analysis; prostate cancer; alkaline phosphatase; prognosis; survival
• ISSN: 1179-1322; 1179-1322
• DOI: 10.2147/cmar.s174237

Many studies have evaluated the relationship between alkaline phosphatase (ALP) and the prognosis for prostate cancer (PCa). But they have not reached a widespread consensus yet. Therefore, we completed a meta-analysis to ascertain the significance of ALP and the prognosis for PCa. A literature search was performed in the PubMed, Embase, and Web of Science databases. HRs concerning overall survival (OS), progression-free survival (PFS), and cancer-specific survival (CSS) were extracted to evaluate the impacts of ALP on the prognosis for PCa. Subgroup analyses were conducted on different study types, regions, sample sizes, and cutoff values. Sensitivity analysis was performed by removing one study in sequence. A total of 63 studies from 54 articles with 16,135 patients were included in this meta-analysis. The pooled results indicated that high baseline ALP was associated with obviously poor OS (HR=1.74, 95% CI: 1.47-2.06) and PFS (HR=1.60, 95% CI: 1.13-2.26) in patients with PCa. The pooled HR for bone-specific ALP and OS was 1.76 (95% CI: 1.45-2.15). However, no association between ALP and CSS (HR=1.002, 95% CI: 0.998-1.005) was found for PCa. The results of subgroup analyses were all in accordance with the main findings. Sensitivity analysis suggested that no single study could affect the stability of the results. High serum ALP is significantly associated with poor OS and PFS except for CSS in PCa. ALP is an efficient and convenient biomarker for PCa prognosis.