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The Multiple Myeloma Hub is an independent medical education platform, sponsored by Bristol Myers Squibb, GSK, Johnson & Johnson, 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.

2025-03-21T12:18:08.000Z

Visual abstract | Belantamab mafodotin in combination with Pd for RRMM: Latest data from DREAMM-8

Mar 21, 2025
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Learning objective: After reading this article, learners will be able to recall the efficacy and safety data for belantamab mafodotin in combination with pomalidomide and dexamethasone for the treatment of relapsed/refractory MM.

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Test your knowledge! Take our quick quiz before and after you read this article to find out if you improved your knowledge. Results help us to improve content and continually provide open-access education.

The Multiple Myeloma Hub presents a visual abstract of the phase III DREAMM-8 study (NCT04484623), which evaluated the combination of belantamab mafodotin, pomalidomide, and dexamethasone (BPd) vs the combination of pomalidomide, bortezomib, and dexamethasone (PVd) for the treatment of patients with relapsed/refractory multiple myeloma (RRMM). The DREAMM-8 study also evaluated the impact of dose modifications and extended treatment intervals on toxicity, efficacy, and quality of life.

 Key takeaways:

  • The BPd combination resulted in a significantly reduced risk of disease progression or death compared with PVd for patients with RRMM, at a hazard ratio of 0.52 (95% CI, 0.37–0.73 [p < 0.001]).
  • There were higher rates of complete response (CR) and an increased duration of response observed with BPd, as well as a higher CR/measurable residual disease rate.
  • While ocular side effects were common with BPd, they were largely manageable with dose modifications, without sacrificing efficacy outcomes.
  • BPd provides a promising option for the treatment of RRMM in the community setting, as well as in areas without access to other targeted therapies, such as bispecific antibodies and chimeric antigen receptor T-cell therapies.


 

As a result of this content, I commit to reviewing the latest clinical data for novel antibody–drug conjugates to help inform my clinical practice.

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This educational resource is independently supported by GSK. All content was developed by SES in collaboration with an expert steering committee; funders were allowed no influence on the content of this resource.

Visual Abstract

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