Literature DB >> 28782211

Bisphosphonate guidelines for treatment and prevention of myeloma bone disease.

Oi Lin Lee1, Noemi Horvath1,2, Cindy Lee2,3, Doug Joshua2,4,5, Joy Ho2,4,5, Jeff Szer2,6,7, Hang Quach2,6,8, Andrew Spencer2,6,9, Simon Harrison2,6,10, Peter Mollee2,11,12, Andrew W Roberts2,6,7,13, Dipti Talaulikar2,14,15, Ross Brown2,4, Bradley Augustson2,16, Silvia Ling2,17,18, Wilfrid Jaksic2,3, John Gibson2,4,5, Anna Kalff2,9, Anna Johnston2,19,20, Akash Kalro2,21, Chris Ward2,5,22, H Miles Prince2,6,10, Andrew Zannettino2,23,24.   

Abstract

Multiple myeloma (MM) is a haematological malignancy characterised by the clonal proliferation of plasma cells in the bone marrow. More than 80% of patients with MM display evidence of myeloma bone disease (MBD), characterised by the formation of osteolytic lesions throughout the axial and appendicular skeleton. MBD significantly increases the risk of skeletal-related events such as pathologic fracture, spinal cord compression and hypercalcaemia. MBD is the result of MM plasma cells-mediated activation of osteoclast activity and suppression of osteoblast activity. Bisphosphonates (BP), pyrophosphate analogues with high bone affinity, are the only pharmacological agents currently recommended for the treatment and prevention of MBD and remain the standard of care. Pamidronate and zoledronic acid are the most commonly used BP to treat MBD. Although generally safe, frequent high doses of BP are associated with adverse events such as renal toxicity and osteonecrosis of the jaw. As such, optimal duration and dosing of BP therapy is required in order to minimise BP-associated adverse events. The following guidelines provide currently available evidence for the adoption of a tailored approach when using BP for the management of MBD.
© 2017 Royal Australasian College of Physicians.

Entities:  

Keywords:  bisphosphonate; myeloma; osteoblast; osteoclast; osteolysis; skeletal-related event (SRE)

Mesh:

Substances:

Year:  2017        PMID: 28782211     DOI: 10.1111/imj.13502

Source DB:  PubMed          Journal:  Intern Med J        ISSN: 1444-0903            Impact factor:   2.048


  5 in total

1.  Circulating cytokines present in multiple myeloma patients inhibit the osteoblastic differentiation of adipose stem cells.

Authors:  Michèle Sabbah; Laurent Garderet; Ladan Kobari; Martine Auclair; Olivier Piau; Nathalie Ferrand; Maurice Zaoui; François Delhommeau; Bruno Fève
Journal:  Leukemia       Date:  2021-09-23       Impact factor: 11.528

2.  Denosumab Versus Zoledronic Acid in Bone Disease Treatment of Newly Diagnosed Multiple Myeloma: An International, Double-Blind, Randomized Controlled Phase 3 Study-Asian Subgroup Analysis.

Authors:  Shang-Yi Huang; Sung-Soo Yoon; Kazuyuki Shimizu; Wee Joo Chng; Cheng-Shyong Chang; Raymond Siu-Ming Wong; Seasea Gao; Yang Wang; Steve W Gordon; Anthony Glennane; Chang-Ki Min
Journal:  Adv Ther       Date:  2020-06-10       Impact factor: 3.845

Review 3.  Role of Osteocytes in Myeloma Bone Disease: Anti-sclerostin Antibody as New Therapeutic Strategy.

Authors:  Denise Toscani; Marina Bolzoni; Marzia Ferretti; Carla Palumbo; Nicola Giuliani
Journal:  Front Immunol       Date:  2018-10-24       Impact factor: 7.561

4.  Systemic Dysfunction of Osteoblast Differentiation in Adipose-Derived Stem Cells from Patients with Multiple Myeloma.

Authors:  Véronique Béréziat; Christelle Mazurier; Martine Auclair; Nathalie Ferrand; Séverine Jolly; Tiffany Marie; Ladan Kobari; Indira Toillon; François Delhommeau; Bruno Fève; Annette K Larsen; Michèle Sabbah; Laurent Garderet
Journal:  Cells       Date:  2019-05-10       Impact factor: 6.600

Review 5.  Bisphosphonate-Based Conjugates and Derivatives as Potential Therapeutic Agents in Osteoporosis, Bone Cancer and Metastatic Bone Cancer.

Authors:  Zintle Mbese; Blessing A Aderibigbe
Journal:  Int J Mol Sci       Date:  2021-06-26       Impact factor: 5.923

  5 in total

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