Koike Takashi, Toyama Daisuke, Shibata Mayuko, Otsuka Kohei, Sugishita Yumiko, Kaneko Ryota, Kawabata Naoko, Fujita Sachio, Akiyama Kosuke, Yamamoto Shohei
Department of Pediatrics, Tokai University School of Medicine, Kanagawa, Japan.
Blood Cell Ther. 2024 Oct 11;7(4):118-120. doi: 10.31547/bct-2024-010. eCollection 2024 Nov 25.
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.
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细胞治疗的前四周内。此外,长期血细胞减少是使用CAR-T细胞疗法后的一种长期不良反应。在此,我们报告一例长期严重血细胞减少后发生致命性CAR-T细胞介导的脑炎病例。一名22岁男性患者因B细胞前体急性淋巴细胞白血病(ALL)第二次复发被转诊至我院,该病在接受来自无关供体的造血干细胞移植22个月后被诊断出来。在化疗后完全缓解的第三个周期输注了CAR-T细胞(tisagenlecleucel)。患者出现2级细胞因子释放综合征,需要单剂量的托珠单抗治疗。从第30天起血细胞减少严重,但未观察到其他严重并发症。在第50天,患者出现感觉障碍、行为紊乱和意识模糊。脑磁共振成像(MRI)扫描和脑脊液(CSF)分析未发现病理结果。尽管使用了粒细胞集落刺激因子(G-CSF)治疗,严重中性粒细胞减少仍持续存在,并且患者的神经症状从第65天开始迅速进展。脑MRI显示脑积水。脑脊液显示黄变、单核细胞计数和蛋白水平升高。用泼尼松龙治疗脑炎的尝试无效,患者于第77天因神经毒性死亡。尽管未对脑脊液进行CAR-T细胞评估,但怀疑是迟发性CAR-T细胞介导的脑炎。此外,患者出现了长期严重的血细胞减少。据我们所知,这是首例关于长期严重血细胞减少后发生迟发性CAR-T细胞介导的脑炎的报告。这些意想不到的长期不良反应可能会发生,也应予以考虑。