Cancer Treatment Reviews
Volume 31, Supplement 3 , Pages 19-25, 2005

Zoledronic acid to prevent skeletal complications in cancer: Corroborating the evidence

Massachusetts General Hospital Cancer Center, Division of Hematology and Oncology, 100 Blossom Street, Cox 640, Boston, MA 02114, USA

Accepted 14 September 2005. published online 17 October 2005.

Summary 

Bone metastases are a major cause of cancer morbidity. Bone metastases are associated with pain, fractures, spinal cord compression, ineffective haematopoiesis, and hypocalcaemia of malignancy. The goals of treatment for bone metastases are to prevent disease-related skeletal complications, palliate pain, and maintain quality of life. Bisphosphonates are a standard part of supportive care for patients with bone metastases. Zoledronic acid, a nitrogen containing third generation bisphosphonate, is the most active and is the most thoroughly investigated bisphosphonate for metastatic bone disease. The efficacy and safety of zoledronic acid has been established in three pivotal prospective, randomized controlled trials involving more than 3000 subjects. The evidence is reviewed here with a focus on clinical relevance. Across a broad array of tumour types, zoledronic acid (4mg intravenously over 15min every 3–4 weeks) decreased the frequency of skeletal-related events, delayed the time to a first skeletal-related event, and reduced pain. Zoledronic acid is more effective than pamidronate in breast cancer and the only bisphosphonate proven effective for metastatic prostate cancer, lung cancer, renal cell carcinoma and other solid tumours.

Keywords: Bone metastases, Cancer induced bone disease, Bisphosphonates, Zoledronic acid, Quality of life, Bone, Breast cancer, Prostate cancer, Multiple myeloma, Lung cancer

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(05)00163-5

doi:10.1016/j.ctrv.2005.09.004

Cancer Treatment Reviews
Volume 31, Supplement 3 , Pages 19-25, 2005