CAR-T(CAR-T)细胞疗法在非肿瘤性疾病中的应用
Chimeric antigen receptor T (CAR-T) cell therapy in non-oncological diseases.
CAR-T(CAR-T)细胞在血液系统恶性肿瘤中的应用推动了这种免疫治疗形式的显著进展。
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Eosinophilic Pleocytosis in the Cerebrospinal Fluid following CAR-T Cell Therapy for Central Nervous System Lymphoma: A Case for Warning?
Eosinophilic Pleocytosis in the Cerebrospinal Fluid following CAR-T Cell Therapy for Central Nervous System Lymphoma: A Case for Warning?
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本报告强调了在 CAR-T 相关神经毒性患者中进行脑脊液分析的重要性,以阐明特定免疫细胞在此类并发症中的作用。
引言:CAR-T(CAR-T)细胞疗法已成为继发性中枢神经系统(CNS)淋巴瘤患者的一种有效治疗选择,但常并发免疫效应细胞相关神经毒性综合征(ICANS)。病例报告:我们报告一例 64 岁女性患者,患有转化型滤泡性淋巴瘤,在接受三线 CAR-T 细胞疗法(tisagenlecleucel)后出现伴嗜酸性粒细胞增多的重度 ICANS。桥接治疗期间患者神经系统状况恶化,并诊断为继发性 CNS 淋巴瘤。经甲氨蝶呤、阿糖胞苷、塞替派和利妥昔单抗方案治疗后,临床及影像学情况改善。CAR-T 细胞输注后,患者发生 II 级细胞因子释放综合征和 III 级 ICANS。由于对糖皮质激素无反应,遂开始使用阿那白滞素,ICANS 完全消退。因血小板减少,脑脊液(CSF)仅在第 +10 天进行分析,发现嗜酸性粒细胞;感染已排除。结论:本病例强调,对 CAR-T 相关神经毒性患者进行脑脊液分析很重要,有助于阐明特定免疫细胞在此类并发症中的作用。
INTRODUCTION: Chimeric antigen receptor T (CAR-T) cell therapy, emerging as an efficient treatment option for patients with secondary central nervous system (CNS) lymphoma, is frequently complicated with immune effector cell-associated neurotoxicity syndrome (ICANS). CASE PRESENTATION: We report a case of a 64-year-old woman with transformed follicular lymphoma, developing high-grade ICANS with eosinophilic pleocytosis following third-line therapy with CAR-T cells (tisagenlecleucel). During bridging therapy, she declined neurologically and was diagnosed with secondary CNS lymphoma. She received methotrexate-cytarabine-thiotepa-rituximab regimen with clinical and radiological improvement. Post-CAR-T cell infusion she developed cytokine release syndrome grade II and ICANS grade III. Given the lack of response to steroids, anakinra was initiated with complete ICANS resolution. Cerebrospinal fluid (CSF) analysis, performed only on day +10 due to thrombocytopenia, revealed eosinophils, while infections were excluded. CONCLUSION: This report emphasizes the importance of CSF analysis in individuals with CAR-T-related neurotoxicity for elucidating the role of specific immune cells in such complications.
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