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B-cell maturation antigen-based therapies post-talquetamab in relapsed or refractory multiple myeloma.
Shrestha, Asis; Alzubi, Marah; Alrawabdeh, Jawad; Schinke, Carolina; Thanendrarajan, Sharmilan; Zangari, Maurizio; van Rhee, Frits; Al Hadidi, Samer.
Afiliação
  • Shrestha A; Department of Hematology/Oncology Myeloma Center Winthrop P. Rockefeller Cancer Institute, University of Arkansas for Medical Sciences Little Rock Arkansas USA.
  • Alzubi M; Department of Medicine, School of Medicine University of Jordan Amman Jordan.
  • Alrawabdeh J; Department of Medicine, School of Medicine University of Jordan Amman Jordan.
  • Schinke C; Department of Hematology/Oncology Myeloma Center Winthrop P. Rockefeller Cancer Institute, University of Arkansas for Medical Sciences Little Rock Arkansas USA.
  • Thanendrarajan S; Department of Hematology/Oncology Myeloma Center Winthrop P. Rockefeller Cancer Institute, University of Arkansas for Medical Sciences Little Rock Arkansas USA.
  • Zangari M; Department of Hematology/Oncology Myeloma Center Winthrop P. Rockefeller Cancer Institute, University of Arkansas for Medical Sciences Little Rock Arkansas USA.
  • van Rhee F; Department of Hematology/Oncology Myeloma Center Winthrop P. Rockefeller Cancer Institute, University of Arkansas for Medical Sciences Little Rock Arkansas USA.
  • Al Hadidi S; Department of Hematology/Oncology Myeloma Center Winthrop P. Rockefeller Cancer Institute, University of Arkansas for Medical Sciences Little Rock Arkansas USA.
EJHaem ; 5(3): 554-559, 2024 Jun.
Article em En | MEDLINE | ID: mdl-38895072
ABSTRACT
Talquetamab recently received approval for relapsed refractory multiple myeloma. However, there is currently no available data on how patients perform with BCMA based agents after progression on talquetamab. Herein, we present the outcome of 10 patients who received BCMA based therapies following talquetamab. The median follow-up was 9.5 months (range 6-24 months). The median progression free survival was 5.5 months (range 1-10 months). Patients had varying grades of cytokine release syndrome and Immune effector cell-associated neurotoxicity syndrome. Our results suggest that treatment with talquetamab followed by BCMA based therapies is feasible and can be considered as clinically indicated.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article