急性淋巴细胞白血病患者的急性严重细胞减少症后致命性CAR - t细胞介导的脑炎。

Blood cell therapy Pub Date : 2024-10-11 eCollection Date: 2024-11-25 DOI:10.31547/bct-2024-010
Takashi Koike, Daisuke Toyama, Mayuko Shibata, Kohei Otsuka, Yumiko Sugishita, Ryota Kaneko, Naoko Kawabata, Sachio Fujita, Kosuke Akiyama, Shohei Yamamoto
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引用次数: 0

摘要

免疫效应细胞相关神经毒性综合征通常发生在嵌合抗原受体(CAR)-T细胞治疗的头四周内。此外,使用CAR -t细胞疗法后,延长的细胞减少是一个长期的不良反应。在这里,我们提出了一个长期严重的细胞减少症,随后是致命的CAR - t细胞介导的脑炎。一名22岁男性患者因b细胞前体急性淋巴母细胞白血病(ALL)第二次复发而转诊至我院,该患者在接受非亲属供者的造血干细胞移植22个月后确诊。在化疗后完全缓解的第三个周期注入CAR - t细胞(tisagenlecleucel)。患者出现2级细胞因子释放综合征,需要单剂量tocilizumab。从第30天开始,细胞减少严重,但未观察到其他严重并发症。第50天,患者出现感觉障碍、不安行为和意识混乱。脑磁共振成像(MRI)扫描和脑脊液(CSF)分析未见病理表现。尽管G-CSF治疗,严重的中性粒细胞减少症仍持续存在,患者的神经系统症状从第65天开始迅速进展。脑部MRI显示脑积水。脑脊液显示黄色血症、单核细胞计数和蛋白水平升高。强的松龙治疗脑炎无效,患者于第77天因神经毒性死亡。怀疑是迟发性CAR - t细胞介导的脑炎,尽管脑脊液未检测CAR - t细胞。此外,患者出现了长期严重的细胞减少症。据我们所知,这是第一次报道慢性严重细胞减少症随后发生迟发性CAR - t细胞介导的脑炎。这些意想不到的长期不良影响可能发生,也应予以考虑。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Prolonged severe cytopenia followed by fatal CAR T-cell-mediated encephalitis in a patient with acute lymphoblastic leukemia.

Prolonged severe cytopenia followed by fatal CAR T-cell-mediated encephalitis in a patient with acute lymphoblastic leukemia.

Immune effector cell-associated neurotoxicity syndrome usually occurs within the first four weeks of chimeric antigen receptor (CAR)-T cell therapy. In addition, prolonged cytopenia is a long-term adverse effect following the use of CAR T-cell therapies. Here, we present a case of prolonged severe cytopenia followed by fatal CAR T-cell-mediated encephalitis. A 22-year-old male patient was referred to our hospital for a second relapse of B-cell precursor acute lymphoblastic leukemia (ALL), which was diagnosed 22 months after hematopoietic stem cell transplantation from an unrelated donor. CAR T-cells (tisagenlecleucel) were infused during the third cycle of complete remission after chemotherapy. The patient developed grade 2 cytokine release syndrome requiring a single dose of tocilizumab. Cytopenia was profound from day 30 onward, but no other serious complications were observed. On day 50, the patient developed sensory impairment, disturbing behavior, and confusion. Brain magnetic resonance imaging (MRI) scan and cerebrospinal fluid (CSF) analysis revealed no pathological findings. Severe neutropenia persisted despite G-CSF treatment, and the patient's neurological symptoms rapidly progressed from day 65. Brain MRI revealed hydrocephalus. The CSF showed elevated xanthochromia, mononuclear cell counts, and protein levels. A therapeutic attempt with prednisolone for encephalitis was ineffective, and the patient died on day 77 owing to neurological toxicity. Late-onset CAR T-cell-mediated encephalitis was suspected, although the CSF was not assessed for CAR T-cells. In addition, the patient developed prolonged and severe cytopenia. To the best of our knowledge, this is the first report of prolonged severe cytopenia followed by late-onset CAR T-cell-mediated encephalitis. These unexpected long-term adverse effects may occur and should also be considered.

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