Advances in the biology and treatment of myeloma bone disease

James R Berenson1

  • 1Multiple Myeloma and Bone Metastasis Program, Cedars-Sinai Medical Center, University of California Las Angeles School of Medicine, 8700 Beverly Boulevard, Bev. Mod. 1, Room 100, Los Angeles, CA 90402, USA.

Seminars in Oncology
|January 10, 2003
PubMed

Insights

Multiple myeloma causes bone loss, leading to fractures and pain. This review covers treatments like osteoprotegerin and bisphosphonates for managing bone disease in myeloma patients.

Area of Science:

  • Oncology
  • Bone Biology
  • Pharmacology

Background:

  • Multiple myeloma frequently causes significant bone loss.
  • Clinical manifestations include pathologic fractures, spinal cord compression, hypercalcemia, and bone pain.

Purpose of the Study:

  • To review the cytokine network in myeloma bone disease.
  • To describe osteoclastogenesis signaling and novel therapeutic mechanisms.
  • To summarize clinical trial results for bisphosphonates in multiple myeloma bone disease.

Main Methods:

  • Review of cytokine networks in myeloma bone disease.
  • Description of osteoclastogenesis signaling pathways.
  • Analysis of novel therapeutic agents including osteoprotegerin, RANK-Fc, PS-341, and bisphosphonates.
  • Summary of clinical trial data for bisphosphonates.

Main Results:

  • The cytokine network plays a crucial role in myeloma-induced bone disease.
  • Novel therapies target key pathways in osteoclast formation and function.
  • Bisphosphonates demonstrate efficacy in managing bone complications.

Conclusions:

  • Understanding the cytokine network is key to managing myeloma bone disease.
  • Targeted therapies offer new avenues for treatment.
  • Bisphosphonates are effective in reducing skeletal-related events in multiple myeloma.

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