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. 2024 May;204(5):1590-1592.
doi: 10.1111/bjh.19439. Epub 2024 Apr 2.

Sequence not salvage

Affiliations

Sequence not salvage

Douglas W Sborov et al. Br J Haematol. 2024 May.

Abstract

Chimeric antigen receptor T-cell (CAR-T) therapy for the treatment of multiple myeloma (MM) has fundamentally changed the relapsed and refractory therapeutic landscape, but the disease remains incurable. Two CAR-T products, idecabtagene vicleucel (ide-cel; Abecma) and ciltacabtagene autoleucel (cilta-cel, Carvykti), have been FDA- and EMA-approved for the treatment of relapsed/refractory MM (RRMM); both target B-cell maturation antigen (BCMA), a surface glycoprotein highly expressed on MM cells. Despite deep and durable responses following CAR-T therapy, most patients will need subsequent treatment, and the optimal next-line therapy is presently unclear. Commentary on: Liu et al. Outcomes in patients with multiple myeloma receiving salvage treatment after BCMA-specific CAR-T therapy: A retrospective analysis of LEGEND-2. Br J Haematol 2024;204:1780-1789.

Keywords: T‐cell redirecting bispecific antibodies; chimeric antigen receptor (CAR) T‐cell therapy; multiple myeloma; proteosome inhibitor.

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References

REFERENCES

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    1. Liu R, Yang R, Xu X, Zhao W, Wang F, Zhang W, et al. Outcomes in patients with multiple myeloma receiving salvage treatment after BCMA‐specific CAR‐T therapy: a retrospective analysis of LEGEND‐2. Br J Haematol. 2024;204:1780–1789.
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