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Mohsin Haematology Academy
EHA 2026 Congress · Stockholm

Myeloma at EHA 2026

A next-generation CELMoD doubling PFS, a bispecific tested in pre-malignant disease, and a GPRC5D-directed phase 3.

Fact-checked 16 June 2026
PositiveNot yet (approval)

SUCCESSOR-2

NCT05552976 · LBA5004 · Dimopoulos · 479 patients

  • Mezigdomide + carfilzomib + dexamethasone vs carfilzomib-dexamethasone
  • Median PFS 18.0 vs 8.3 months, HR 0.48, P<0.0001
  • Neutropenia in line with expectations; discontinuation for it was rare
  • Published in the Lancet on 14 June 2026

Why it matters: A next-generation CELMoD roughly doubled PFS and could become an accessible combination across care settings once approved.

PositiveInvestigational

ImmunoPRISM

Immuno-PRISM · NCT05469893 · Nadeem · phase 2

  • Teclistamab vs lenalidomide-dexamethasone in high-risk smouldering myeloma
  • Estimated 2-year PFS 92% vs 51%
  • MRD-negativity at 10⁻⁵ of 81.2% vs 0%
  • Complete response 75.6% vs none; no high-grade CRS or neurotoxicity

Why it matters: Striking depth of response, but this is phase 2 bispecific therapy in pre-malignant disease, so the risk-benefit balance needs longer follow-up.

WatchWatch

MonumenTAL-3

Talquetamab (GPRC5D) vs DPd

  • Phase 3 talquetamab-based regimens vs daratumumab-pomalidomide-dexamethasone
  • GPRC5D toxicity: dysgeusia, skin and nail changes, weight loss from taste disturbance
  • Note: MajesTEC-9 is a separate teclistamab monotherapy trial presented at ASCO 2026, not EHA

Why it matters: Bispecifics continue to move into earlier myeloma lines; specific EHA 2026 efficacy figures for MonumenTAL-3 were not independently verified here.

Treating disease earlier raises the bar for proving benefit outweighs harm.ImmunoPRISM moved bispecific therapy into pre-malignant smouldering myeloma.