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  1. OncLive® On Air
  2. S14 Ep75: FDA Approval Insights: BVd for Relapsed/Refractory Multiple Myeloma: With Surbhi Sidana, MD
S14 Ep75: FDA Approval Insights: BVd for Relapsed/Refractory Multiple Myeloma: With Surbhi Sidana, MD

S14 Ep75: FDA Approval Insights: BVd for Relapsed/Refractory Multiple Myeloma: With Surbhi Sidana, MD

OncLive® On Air · Jan 9, 2026

FDA approves belantamab mafodotin for myeloma, a new community-based option. Key challenges: ocular toxicity management & sequencing with CAR-T.

Belantumab's Survival Benefit Over Daratumumab Sets a New Efficacy Benchmark in Myeloma

The DREAM-7 trial showed a belantumab combination had an overall survival benefit versus a daratumumab regimen, a "premier drug" that previously changed the myeloma treatment landscape. This surprising result establishes a new, higher standard of care and positions belantumab as a top-tier therapy, not merely another option.

S14 Ep75: FDA Approval Insights: BVd for Relapsed/Refractory Multiple Myeloma: With Surbhi Sidana, MD thumbnail

S14 Ep75: FDA Approval Insights: BVd for Relapsed/Refractory Multiple Myeloma: With Surbhi Sidana, MD

OncLive® On Air·a month ago

Real-World Belantumab Dosing Requires Aggressive Reductions from the Approved Start Dose

Due to significant ocular toxicity affecting most patients, the approved starting dose for belantumab is likely not optimal long-term. Effective management requires clinicians to proactively hold, delay, and reduce doses at the first sign of side effects, meaning real-world application will differ from the initial protocol.

S14 Ep75: FDA Approval Insights: BVd for Relapsed/Refractory Multiple Myeloma: With Surbhi Sidana, MD thumbnail

S14 Ep75: FDA Approval Insights: BVd for Relapsed/Refractory Multiple Myeloma: With Surbhi Sidana, MD

OncLive® On Air·a month ago

Belantumab Creates a Strategic Dilemma: Prioritize Community Access Now or Preserve Future CAR-T Efficacy?

Clinicians must weigh the immediate benefit of using community-accessible belantumab against the risk of reducing the efficacy of future BCMA-targeted therapies like CAR-T or bispecifics. This decision hinges on a patient's ability to travel and access advanced care, creating a complex treatment sequencing challenge.

S14 Ep75: FDA Approval Insights: BVd for Relapsed/Refractory Multiple Myeloma: With Surbhi Sidana, MD thumbnail

S14 Ep75: FDA Approval Insights: BVd for Relapsed/Refractory Multiple Myeloma: With Surbhi Sidana, MD

OncLive® On Air·a month ago