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Multiple Myeloma: 2026 Update on Diagnosis, Risk‐Stratification and Management

American Journal of Hematology·August 18
HematologyPractice changingMultiple MyelomaSmoldering Multiple MyelomaNarrative Review / Clinical Practice UpdateAnti-CD38 Monoclonal AntibodyAntibody-Drug ConjugateAutologous Stem Cell TransplantationBispecific AntibodyCAR-T Cell TherapyImmunomodulatory DrugProteasome InhibitorAdultDarzalexSarclisaBelantamab MafadotinBortezomibDaratumumabDexamethasoneIsatuximabLenalidomide

Summary

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What was studied

A comprehensive 2026 update on the diagnosis, risk-stratification, and management of multiple myeloma (MM), covering criteria for MM-defining events, high-risk cytogenetic definitions, frontline quadruplet regimens, maintenance strategies, and relapsed/refractory options.

Key findings

Frontline standard-of-care is now a quadruplet (anti-CD38 + bortezomib/lenalidomide/dexamethasone) followed by ASCT in eligible patients; high-risk MM is redefined to include bi-allelic del(1p), combination cytogenetic lesions with gain(1q) or del(1p), and p53 mutation; daratumumab for 3 years is recommended for high-risk smoldering MM.

Study limitations

This is a narrative review/guideline update, not a primary clinical trial — it synthesizes existing evidence without new original data or formal meta-analysis.

Clinical implications

Upgrade frontline-eligible patients to anti-CD38–based quadruplet therapy (Dara- or Isa-VRd) and reassess high-risk status using the expanded cytogenetic criteria including gain(1q)/del(1p) combinations. For high-risk smoldering MM, consider 3 years of daratumumab to delay progression.

Caveats

  • Brand name 'Darzalex' listed for daratumumab; isatuximab brand 'Sarclisa' inferred from common knowledge — not explicitly stated in the abstract.
  • The label 'practice_changing' reflects major updates to both risk stratification criteria and frontline quadruplet therapy recommendations.
  • The paper was published August 18, 2026, just 6 days before today's date; some referenced trials or approvals may be very recent and not yet widely implemented.
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  • This is a guideline/review article, not a primary trial — level of evidence reflects expert synthesis, not a controlled study. No sample size is applicable.

Related Questions

Explore related topics

What is the evidence for daratumumab-VRd quadruplet therapy versus triplet in newly diagnosed myeloma?How should high-risk smoldering myeloma be treated with daratumumab in 2025–2026?When should CAR-T or bispecific antibodies be used in relapsed/refractory multiple myeloma?

Publication Details

Year
2026
Journal
American Journal of Hematology
Source
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