4.4 Review

Alkaline phosphatase in metastatic castration-resistant prostate cancer: reassessment of an older biomarker

期刊

FUTURE ONCOLOGY
卷 14, 期 24, 页码 2543-2556

出版社

FUTURE MEDICINE LTD
DOI: 10.2217/fon-2018-0087

关键词

alkaline phosphatase; biomarker; bone metastases; castration-resistant prostate cancer; mechanism of action; prognostic marker; survival

类别

资金

  1. Bayer
  2. Janssen-Cilag (Johnson Johnson)
  3. Merck Sharp Dohme
  4. Roche
  5. Bayer HealthCare Pharmaceuticals, LLC
  6. Takeda
  7. Astellas
  8. Daiichi-Sankyo
  9. Pfizer
  10. Taiho
  11. Nihon-Kayaku
  12. Endocyte
  13. Innocrin
  14. Johnson Johnson
  15. Sanofi-Aventis
  16. Bayer HealthCare Pharmaceuticals

向作者/读者索取更多资源

Since most patients with metastatic castration-resistant prostate cancer (mCRPC) have bone metastases, it is important to understand the potential impact of therapies on prognostic biomarkers, such as ALP. Clinical studies involving mCRPC life-prolonging agents (i.e., sipuleucel-T, abiraterone, enzalutamide, docetaxel, cabazitaxel, and radium-223) have shown that baseline ALP level is prognostic for overall survival, and may be a better prognostic marker for overall survival than prostate-specific antigen in patients with bone-dominant mCRPC. Mechanism of action differences between therapies may partly explain ALP dynamics during treatment. ALP changes can be interpreted within the context of other parameters while monitoring disease activity to better understand the underlying pathology. This review evaluates the current role of ALP in mCRPC.

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