CAR-T-细胞治疗复发性/难治性伯基特淋巴瘤后骨髓再生障碍。

Troy J Kenkel, Nithya Sridhar, Lindsay R Hammons, Maria Hintzke, Nirav N Shah
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引用次数: 0

摘要

嵌合抗原受体T细胞(CAR-T)现在是治疗复发/难治性B细胞淋巴瘤的标准方法。免疫效应细胞相关的噬血细胞性淋巴组织细胞增多症样综合征(IEC-HS)是一种新描述的实体,可在CAR-T后表现出来。骨髓(BM)再生障碍是CAR-T细胞治疗后报道的IEC-HS的一种罕见表现,被定义为造血祖细胞减少或缺失,导致严重的全血细胞减少。我们描述了一例44岁的女性复发/难治性伯基特淋巴瘤(BL)患者,她接受了利索卡布他涅-马拉亮氨酸治疗,其CAR-T后病程合并细胞因子释放综合征(CRS)和IEC-HS,最终导致持续性骨髓再生障碍。她接受了挽救性异基因干细胞移植,但最终死于进行性疾病。IEC-HS是一种越来越被认可的并发症,发生在CAR-T治疗后,可能导致发育不全,这是一种危险的并发症,具有严重的后遗症,包括感染、输血依赖和出血的高风险。其潜在机制尚不清楚,需要进一步研究以了解如何更好地治疗它。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Bone Marrow Aplasia after CAR-T-Cell Therapy for Relapsed/Refractory Burkitt's Lymphoma.

Chimeric antigen receptor T-cells (CAR-T) are now a standard approach for treating relapsed/refractory B-cell lymphomas. Immune effector cell-associated hemophagocytic lymphohistiocytosis-like syndrome (IEC-HS) is a newly described entity that can manifest following CAR-T. Bone marrow (BM) aplasia is an uncommon manifestation of IEC-HS reported after CAR-T-cell therapy and is defined as the reduction or absence of hematopoietic progenitor cells resulting in severe pancytopenia. We describe the case of a 44-year-old female with relapsed/refractory Burkitt lymphoma (BL) who received treatment with lisocabtagene maraleucel with her post-CAR-T course complicated by cytokine release syndrome (CRS) and IEC-HS ultimately leading to persistent BM aplasia. She underwent a rescue allogeneic stem cell transplant but ultimately succumbed to progressive disease. IEC-HS is an increasingly recognized complication that occurs after CAR-T treatments that can result in aplasia, a dangerous complication with serious sequelae including infection, transfusion dependence, and high risk for hemorrhage. The underlying mechanism is poorly understood, and further studies are needed to understand how to treat it better.

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