Cancer Treatment Reviews
Volume 29, Issue 3 , Pages 189-198, June 2003

Pathophysiology of bone metastases from prostate cancer and the role of bisphosphonates in treatment

  • Colby L Eaton

      Affiliations

    • Academic Urology Unit, University of Sheffield, Sheffield, UK
    • Corresponding Author InformationCorrespondence to: Colby L. Eaton, Lecturer, Academic Urology Unit, University of Sheffield, Royal Hallamshire Hospital, Sheffield S10 2JF
  • ,
  • R.E Coleman

      Affiliations

    • Professor of Medical Oncology, Academic Unit of Clinical Oncology, Cancer Research Centre, Weston Park Hospital, Sheffield S10 2SJ, UK

Abstract 

Metastasis to bone is a common feature in advanced prostate cancer patients. Current treatments, while effective in suppressing tumour growth and relieving tumour associated bone pain, do not provide long term remission or ‘cure’ for the disease. A greater understanding of prostate cancer metastasis is required if new treatment strategies are to be developed. Growth of tumour foci in skeletal sites is a major cause of morbidity in advanced prostate cancer and has required the development of specialised approaches to treatment, including the use of bisphosphonates. These drugs inhibit tumour induced osteoclastic bone resorption, thereby preventing skeletal related events and treatment induced bone loss. Zoledronic acid is currently the only bisphosphonate with proven benefit in prostate cancer. Bisphosphonates may also modify the bone microenvironment so that it becomes less favourable for the growth and survival of metastases. The most recent developments in our understanding of the advantages for growth and survival gained by metastatic prostate cancer cells in the skeleton are reviewed, along with the clinical evidence supporting the use of bisphosphonates in advanced prostate cancer.

Keywords:  Bone, metastasis, prostate cancer, bisphosphonates

To access this article, please choose from the options below

Login to an existing account or Register a new account.

  • Purchase this article for 31.50 USD (You must login/register to purchase this article)

    Online access for 24 hours. The PDF version can be downloaded as your permanent record.

  • Subscribe to this title

    Get unlimited online access to this article and all other articles in this title 24/7 for one year.

  • Claim access now

    For current subscribers with Society Membership or Account Number.

  • Visit SciVerse ScienceDirect to see if you have access via your institution.
 

PII: S0305-7372(03)00071-9

doi:10.1016/S0305-7372(03)00071-9

Cancer Treatment Reviews
Volume 29, Issue 3 , Pages 189-198, June 2003