Association of genetic ancestry with outcomes and toxicity of idecabtagene vicleucel in patients with relapsed/refractory multiple myeloma - Summary - MDSpire

Association of genetic ancestry with outcomes and toxicity of idecabtagene vicleucel in patients with relapsed/refractory multiple myeloma

  • By

  • Christen M. Dillard

  • Hans Lee

  • Nilesh Kalariya

  • Naveen Subramanian

  • Oren Pasvolsky

  • Christopher Ferreri

  • Mahmoud Gaballa

  • Sheeba K. Thomas

  • Donna M. Weber

  • Melody Becnel

  • Gregory Kaufman

  • Muzaffar Qazilbash

  • Robert Z. Orlowski

  • Michelle A. T. Hildebrandt

  • Krina K. Patel

  • April 13, 2026

  • 0 min

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Objective:

To investigate the associations between genetic ancestry and CAR-T outcomes in patients with relapsed/refractory multiple myeloma (RRMM), highlighting the significance of these outcomes.

Key Findings:
  • No significant differences in overall response rate (ORR), progression-free survival (PFS), or overall survival (OS) by genetic ancestry, suggesting the need for tailored treatment strategies.
  • Patients with higher African ancestry (AFR) exhibited more aggressive disease features, indicating a potential need for more intensive treatment.
  • Patients with higher European ancestry (EUR) had fewer prior lines of therapy and lower rates of organ involvement, which may influence treatment decisions.
Interpretation:

Genetic ancestry may provide a more precise understanding of biologically relevant factors influencing CAR-T therapy outcomes, despite no significant differences in efficacy or safety observed; further research is essential to explore these associations.

Limitations:
  • Single-center study may limit generalizability and introduce bias.
  • Retrospective design may introduce bias, and potential confounding factors should be considered.
  • Small sample size for certain ancestry groups limits the robustness of findings.
Conclusion:

Genetic ancestry is a relevant factor in understanding treatment outcomes in RRMM, but further research is needed to clarify its impact on CAR-T therapy, particularly in diverse populations.

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