All content on this site is intended for healthcare professionals only. By acknowledging this message and accessing the information on this website you are confirming that you are a Healthcare Professional. If you are a patient or carer, please visit the International Myeloma Foundation or HealthTree for Multiple Myeloma.
Introducing
Now you can personalise
your Multiple Myeloma Hub experience!
Bookmark content to read later
Select your specific areas of interest
View content recommended for you
Find out moreThe Multiple Myeloma Hub website uses a third-party service provided by Google that dynamically translates web content. Translations are machine generated, so may not be an exact or complete translation, and the Multiple Myeloma Hub cannot guarantee the accuracy of translated content. The Multiple Myeloma Hub and its employees will not be liable for any direct, indirect, or consequential damages (even if foreseeable) resulting from use of the Google Translate feature. For further support with Google Translate, visit Google Translate Help.
The Multiple Myeloma Hub is an independent medical education platform, sponsored by Bristol Myers Squibb, GSK, Pfizer, Roche and Sanofi. The levels of sponsorship listed are reflective of the amount of funding given. Digital educational resources delivered on the Multiple Myeloma Hub are supported by an educational grant from Janssen Biotech, Inc. View funders.
Bookmark this article
Multiple myeloma accounts for 1% of all cancers and 10% of all hematologic malignancies, with an annual age-adjusted incidence rate of 4 per 100,000 in the US.1 A 2024 update on the diagnosis, risk stratification, and management of patients with multiple myeloma was published in the American Journal of Hematology by Rajkumar.1 |
Key learnings |
The updated IMWG guidelines require ≥10% clonal plasma cells plus evidence of ≥1 MDE, CRAB features, and three specific biomarkers, ≥60% clonal bone marrow plasma cells, serum FLC ratio ≥100, and ≥1 focal lesion detected by MRI. Incorporating these biomarkers enables an earlier diagnosis and allows treatment before organ damage occurs. |
The RISS and Mayo Clinic mSMART risk stratification incorporate tumor burden, high-risk cytogenetic markers, and elevated lactate dehydrogenase levels to identify high-risk patients and guide therapeutic strategies. |
For TE patients with NDMM, the initial treatment option includes Dara-VRd or Isa-VRd, followed by auto-HSCT. For TI patients with NDMM, the initial treatment option includes either VRd or DRd if they are frail and Dara-VRD or Isa-VRD if they are not frail. |
Lenalidomide maintenance is the standard of care for most patients, while high-risk patients benefit from a combination of bortezomib and lenalidomide. |
Treatment for patients with RRMM is based on several factors, including the timing of relapse, response to prior therapy, aggressiveness of the relapse, and performance status. |
Abbreviations: auto-HSCT, autologous hematopoietic stem cell transplantation; CRAB, hypercalcemia, renal failure, anemia, or lytic bone lesions; Dara-VRd, daratumumab, bortezomib, lenalidomide, dexamethasone; DRd, daratumumab, lenalidomide, dexamethasone; FLC, free light chain; IMWG, International Myeloma Working Group; Isa-VRd, isatuximab, bortezomib, lenalidomide, dexamethasone; MDE, myeloma-defining event; MRI, magnetic resonance imaging; NDMM, newly diagnosed multiple myeloma; RISS, revised International Staging System; RRMM, relapsed/refractory multiple myeloma; TE, transplant-eligible; TI, transplant-ineligible; VRd, bortezomib, lenalidomide, dexamethasone.
Your opinion matters
Subscribe to get the best content related to multiple myeloma delivered to your inbox