Molecular mechanisms, current management and next generation therapy in myeloma bone disease

Roy Heusschen, Joséphine Muller, Elodie Duray, Nadia Withofs, Arnold Bolomsky, Frédéric Baron, Yves Beguin, Eline Menu, Heinz Ludwig, Jo Caers

Research output: Contribution to journalArticlepeer-review

19 Citations (Scopus)
148 Downloads (Pure)

Abstract

Multiple myeloma (MM) bone disease is a major cause of morbidity and mortality in MM patients and persists even in patients in remission. This bone disease is caused by an uncoupling of bone remodeling, with increased osteoclast and decreased osteoblast activity and formation, culminating in lytic bone destruction. Bisphosphonates are the current standard of care but new therapies are needed. As the molecular mechanisms controlling MM bone disease are increasingly well understood, new therapeutic targets are extensively explored in the preclinical setting and initial clinical trials with novel compounds now show promising results. In this review, we will provide a comprehensive overview of the biology of MM bone disease, summarize its current clinical management and discuss preclinical and clinical data on next generation therapies.

Original languageEnglish
Pages (from-to)14-28
Number of pages15
JournalLeukemia & Lymphoma
Volume59
Issue number1
DOIs
Publication statusPublished - 2 Jan 2018

Keywords

  • bisphosphonates
  • bone disease
  • clinical trials
  • Multiple myeloma
  • novel therapies
  • Bone Resorption/drug therapy
  • Multiple Myeloma/complications
  • Bone Diseases/diagnosis
  • Signal Transduction
  • Bone Density Conservation Agents/pharmacology
  • Humans
  • Osteoclasts/drug effects
  • Tumor Microenvironment
  • Diphosphonates/pharmacology
  • Treatment Outcome
  • Clinical Trials as Topic
  • Osteoblasts/drug effects
  • Osteogenesis/drug effects
  • Animals
  • Disease Management
  • Drug Evaluation, Preclinical
  • Bone Remodeling
  • Bone Marrow/drug effects

Fingerprint

Dive into the research topics of 'Molecular mechanisms, current management and next generation therapy in myeloma bone disease'. Together they form a unique fingerprint.

Cite this