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EHA 2025 | Updated results from DREAMM-8: belamaf plus pomalidomide and dexamethasone in R/R myeloma

Meletios Dimopoulos, MD, Kapodistrian University of Athens School of Medicine, Athens, Greece, comments on the updated results of the DREAMM-8 study (NCT04484623), a Phase III trial comparing belantamab mafodotin (belamaf) plus pomalidomide and dexamethasone to pomalidomide plus bortezomib and dexamethasone in patients with relapsed/refractory (R/R) multiple myeloma (MM) who have been pre-treated with lenalidomide or anti-CD38 monoclonal antibodies. Prof. Dimopoulos highlights that the investigational arm demonstrated improved progression-free survival (PFS), and the toxicity profile of the belamaf combination was as expected. This interview took place at the 30th Congress of the European Hematology Association (EHA) in Milan, Italy.

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Transcript

The DREAMM-8 study, which has been published a few months ago, is a prospective randomized trial which is comparing the activity of pomalidomide, bortezomib, and dexamethasone as the control arm with the combination of belantamab mafodotin with pomalidomide and dexamethasone as the investigational arm. The importance of this study is that it includes patients who have been pre-treated with lenalidomide, and this is the majority of the patients with myeloma today, but also it included patients who were pre-treated with anti-CD38 monoclonal antibody, daratumumab or isatuximab, and this is an increasing patient population based on the current standard care...

The DREAMM-8 study, which has been published a few months ago, is a prospective randomized trial which is comparing the activity of pomalidomide, bortezomib, and dexamethasone as the control arm with the combination of belantamab mafodotin with pomalidomide and dexamethasone as the investigational arm. The importance of this study is that it includes patients who have been pre-treated with lenalidomide, and this is the majority of the patients with myeloma today, but also it included patients who were pre-treated with anti-CD38 monoclonal antibody, daratumumab or isatuximab, and this is an increasing patient population based on the current standard care. 

In this study, we report in this meeting that there is an improved progression-free survival and the median is 32 months, meaning that with a combination of belantamab given on an outpatient basis, you can achieve an almost three-year median progression-free survival in patients with myeloma who have been pre-treated and most of them are resistant to lenalidomide but also to daratumumab or isatuximab. 

The toxicity of the combination was as expected, with ocular issues that are associated with belantamab, but with appropriate dose adjustment and holding belantamab until there is a recovery of the high toxicity, the majority of the patients remained on study and actually were able to benefit from this very active combination.

 

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Disclosures

Amgen, Sanofi, Regeneron, Menarini, Takeda, GSK, BMS, Janssen, Beigene, Swixx, AstraZeneca