TY - JOUR
T1 - Updated guidelines in the treatment of myeloma bone disease in 2025
T2 - consensus statement by the Medical and Scientific Advisory Group of Australia (MSAG) to Myeloma Australia
AU - on behalf of Medical Scientific Advisory Group to Myeloma Australia
AU - Yong, Angelina
AU - Vandyke, Kate
AU - Augustson, Bradley
AU - McCaughan, Georgia
AU - Talaulikar, Dipti
AU - Szabo, Ferenc
AU - Prince, Henry Miles
AU - Ho, Phoebe Joy
AU - Quach, Hang
AU - Harrison, Simon J.
AU - Lee, Cindy Hs
N1 - Publisher Copyright:
© 2025 Informa UK Limited, trading as Taylor & Francis Group.
PY - 2026/1
Y1 - 2026/1
N2 - Introduction: Multiple myeloma is a hematological malignancy characterized by clonal plasma cell proliferation within the bone marrow, often resulting in osteolytic bone disease. Traditionally, bisphosphonates, such as zoledronic acid and pamidronate, have been used in the prophylaxis and treatment of myeloma bone disease (MBD). Areas covered: A comprehensive, systematic review using these keywords, ‘multiple myeloma,’ ‘myeloma bone disease,’ ‘bisphosphonates,’ ‘denosumab,’ ‘osteonecrosis’ was conducted on Medline and Cochrane databases from 1995 to 2024. Priority was given articles reporting randomized, double-blinded clinical trials; with inclusion of large case cohort studies, in view of the limited comparison between different bone resorptive agents in the treatment of myeloma bone disease. Expert opinion: This updated guideline recommends a two-year course of bisphosphonate treatment, with suggested extension of dosing intervals if the disease remains stable. Denosumab, a monoclonal antibody targeting receptor activator of nuclear factor ϰB ligand (RANKL), has demonstrated efficacy and non-inferiority compared to zoledronic acid in the treatment of MBD and may serve as an alternative treatment option especially with renal impairment. Further research into the utility of bone turnover markers for guiding anti-resorptive therapy in myeloma bone disease may provide significant clinical benefit. In addition, therapeutic strategies aimed at enhancing osteoblastic activity represent a potential therapeutic strategy.
AB - Introduction: Multiple myeloma is a hematological malignancy characterized by clonal plasma cell proliferation within the bone marrow, often resulting in osteolytic bone disease. Traditionally, bisphosphonates, such as zoledronic acid and pamidronate, have been used in the prophylaxis and treatment of myeloma bone disease (MBD). Areas covered: A comprehensive, systematic review using these keywords, ‘multiple myeloma,’ ‘myeloma bone disease,’ ‘bisphosphonates,’ ‘denosumab,’ ‘osteonecrosis’ was conducted on Medline and Cochrane databases from 1995 to 2024. Priority was given articles reporting randomized, double-blinded clinical trials; with inclusion of large case cohort studies, in view of the limited comparison between different bone resorptive agents in the treatment of myeloma bone disease. Expert opinion: This updated guideline recommends a two-year course of bisphosphonate treatment, with suggested extension of dosing intervals if the disease remains stable. Denosumab, a monoclonal antibody targeting receptor activator of nuclear factor ϰB ligand (RANKL), has demonstrated efficacy and non-inferiority compared to zoledronic acid in the treatment of MBD and may serve as an alternative treatment option especially with renal impairment. Further research into the utility of bone turnover markers for guiding anti-resorptive therapy in myeloma bone disease may provide significant clinical benefit. In addition, therapeutic strategies aimed at enhancing osteoblastic activity represent a potential therapeutic strategy.
KW - Multiple myeloma
KW - bisphosphonates
KW - denosumab
KW - fractures
KW - lytic lesions
KW - myeloma bone disease
KW - osteonecrosis of the jaw
KW - renal impairment
KW - zoledronic acid
UR - https://www.scopus.com/pages/publications/105025405715
U2 - 10.1080/17474086.2025.2574716
DO - 10.1080/17474086.2025.2574716
M3 - Review article
C2 - 41082262
AN - SCOPUS:105025405715
SN - 1747-4086
VL - 19
SP - 133
EP - 142
JO - Expert Review of Hematology
JF - Expert Review of Hematology
IS - 2
ER -