New classification for identifying HR myeloma based on cytogenetic abnormalities
Induction regimen for transplant eligible multiple myeloma (MM) patients is 4-6 course of a triple drug regimen, typically with bortezomib, dexamethasone and cyclophosphamide (VCD), followed by ASCT. In some centres the alkylating agent may be substituted with thalidomide (VTD) or lenalidomide. Important factors determining which treatment to consider include effectiveness, tolerability and availability for first-line use.
The use of consolidation after ASCT may provide additional benefit, but this is still to be confirmed. It is being investigated in a number of trials, but Phase III data are needed and it is not routinely used outside of a clinical trial.
Maintenance with thalidomide has demonstrated improvements in progression free survival (PFS) and overall survival (OS). Lenalidomide has also demonstrated a significant PFS benefit, but not OS benefit. Maintenance is seen as an attractive treatment option for transplant MM candidates but is still confined to use in the clinical trial setting.
Delaying transplant may be a viable option for some patients. However, the recommendation is that all eligible patients should be offered ASCT.
This programme has been supported by an unrestricted educational grant from Janssen Pharmaceutica (A Johnson & Johnson Company).
New classification for identifying HR myeloma based on cytogenetic abnormalities
Daratumumab, bortezomib/thalidomide/dexamethasone (D-VTd) and DARA maintenance shows benefit in transplant-eligible NDMM
Isatuximab plus lenalidomide and dexamethasone with bortezomib as a new standard of care for NDMM TI non-frail patients
Made to measure: Choosing the optimal regimen in transplant-eligible NDMM
Use of bispecifics and CAR T cells in South America
Revolutionising myeloma treatment through immune profiling
Treating relapsed multiple myeloma outside of use of T-cell redirected therapies
Guiding transplant decisions in multiple myeloma with MRD
Revolutionising multiple myeloma treatment with CAR T-Cell therapies