B-cell maturation antigen-based therapies post-talquetamab in relapsed or refractory multiple myeloma

EJHaem Pub Date : 2024-04-16 DOI:10.1002/jha2.896
Asis Shrestha, Marah Alzubi, Jawad Alrawabdeh, Carolina Schinke, Sharmilan Thanendrarajan, Maurizio Zangari, Frits van Rhee, Samer Al Hadidi
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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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复发或难治性多发性骨髓瘤患者在使用他曲单抗后使用基于 B 细胞成熟抗原的疗法
Talquetamab 最近获批用于治疗复发难治性多发性骨髓瘤。然而,目前尚无数据显示患者在使用塔雷克单抗治疗进展期后使用基于BCMA的药物的疗效。在此,我们介绍了10名患者在使用塔雷克单抗后接受BCMA类药物治疗的结果。中位随访时间为 9.5 个月(6-24 个月)。中位无进展生存期为5.5个月(范围:1-10个月)。患者出现了不同程度的细胞因子释放综合征和免疫效应细胞相关神经毒性综合征。我们的研究结果表明,在使用塔利奎单抗治疗后,再使用基于BCMA的疗法是可行的,临床上可以考虑使用。
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