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Sequence not salvage.
Sborov, Douglas W; Fortuna, Gliceida Galarza; Hayden, Patrick J.
Affiliation
  • Sborov DW; Huntsman Cancer Institute at the University of Utah, Salt Lake City, Utah, USA.
  • Fortuna GG; Huntsman Cancer Institute at the University of Utah, Salt Lake City, Utah, USA.
  • Hayden PJ; Department of Haematology, School of Medicine, St. James's Hospital, Trinity College, Dublin, Ireland.
Br J Haematol ; 204(5): 1590-1592, 2024 May.
Article de En | MEDLINE | ID: mdl-38563345
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;2041780-1789.
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Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Immunothérapie adoptive / Thérapie de rattrapage / Myélome multiple Limites: Humans Langue: En Journal: Br J Haematol Année: 2024 Type de document: Article Pays d'affiliation: États-Unis d'Amérique

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Immunothérapie adoptive / Thérapie de rattrapage / Myélome multiple Limites: Humans Langue: En Journal: Br J Haematol Année: 2024 Type de document: Article Pays d'affiliation: États-Unis d'Amérique
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