血浆交换治疗抗cd19嵌合抗原受体- t细胞输注后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:一例报告

Yan Qiu, Wenjie Gong, Liqing Kang, A. Sun, De-pei Wu, Lei Yu, Jian Zhang, S. Xue
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摘要

嵌合抗原受体- t (CAR-T)细胞过继细胞免疫治疗已显示出显著的临床效果。然而,细胞因子释放综合征(CRS)和免疫效应细胞相关神经毒性综合征(ICANS)是这种治疗过程中最显著的两种毒性,可能危及生命。我们描述了一个12岁的少年,他被诊断为复发和难治性b细胞急性淋巴细胞白血病(r/r B-ALL)。该患者被纳入我们关于ssCAR-T-19(具有shRNA靶向IL-6的抗cd19 CAR-T细胞)的I期临床试验,并给予5*106 /kg的工程化ssCAR-T-19细胞。输注后,患者出现典型的CRS反应,伴有发热和细胞因子水平升高。他接受了退烧药、甲基强的松龙和托珠单抗治疗,但效果有限。患者出现凝血功能异常、多器官功能障碍、肺部感染和ICANS。除必要的支持和对症治疗外,4天内进行3次血浆置换,连续2天进行甲基强的松龙脉冲治疗。之后,体温、心率,尤其是细胞因子水平下降。但他发生消化道出血,被转到重症监护室。更糟糕的是,他出现了急性呼吸衰竭,接受了插管和机械通气。同时给予抑胃酸、抗感染等对症治疗。出血得到控制,呼吸功能得到改善,CRS和icans相关症状得到缓解。他拔管后被转回普通病房。此外,以上骨髓涂片未见淋巴母细胞,骨髓微量残留病变在第22天和第30天阴性。病人最终出院,情况正常。总之,CRS和ICANS是CAR-T治疗后最常见的两种毒性,通常会导致患者死亡。除血浆置换外,CRS和ICANS的管理指南中已采用几种方法,如抗il -6治疗和/或皮质类固醇。该病例表明,在接受ssCAR-T治疗后,血浆置换对严重CRS和ICANS患者是有效的。
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Plasma Exchange to Treat Cytokine Release Syndrome and Immune Effector Cell-Associated Neurotoxicity Syndrome after Anti-CD19 Chimeric Antigen Receptor-T Cell Infusion: A Case Report
Adoptive cell immunotherapy with chimeric antigen receptor-T (CAR-T) cells has shown remarkable clinical outcomes. However, cytokine release syndrome (CRS) and immune effector cell-associated neurotoxicity syndrome (ICANS) are the two most significant toxicities during this therapy and can be life-threatening. We described a 12-year-old juvenile who had been diagnosed with relapsed and refractory B-cell acute lymphocytic leukemia (r/r B-ALL). The patient was recruited into our phase I clinical trial concerning ssCAR-T-19 (anti-CD19 CAR-T cells with shRNA targeting IL-6), and 5*106 /kg of engineered ssCAR-T-19 cells were administered. After infusion, the patient underwent a typical CRS reaction, with fever and increased cytokine levels. He was treated with antipyretic drugs, methylprednisolone, and tocilizumab, but the effect was limited. He developed coagulation abnormalities, multiple organ dysfunction, lung infection and ICANS. Apart from the necessary supportive and symptomatic treatment, plasma exchange was performed three times in four days while methylprednisolone pulse was performed for two consecutive days. After that, the body temperature, heart rate, and especially the cytokine levels declined. But digestive tract hemorrhage occurred to him and he was transferred to intensive care unit. To make things worse, he developed acute respiratory failure and received intubation and mechanical ventilation. In addition, symptomatic treatment such as suppression of stomach acid and anti-infection was given. The bleeding was controlled, and his respiratory function improved, and the CRS and ICANS-related symptoms were relieved. He received extubation and was transferred back to the general ward. Additionally, abone marrow smear showed no lymphoblast cells, and minimal residual disease in bone marrow was negative on day +22 and day +30. The patient was eventually discharged in a normal condition. In conclusion, CRS and ICANS as two most common toxicities after CAR-T therapy, which often cause patient death. Several methods such as anti-IL-6 therapy and/or corticosteroids have been adopted in the management guidelines of CRS and ICANS except plasma exchange. This case shows the validity of plasma exchange in a patient with severe CRS and ICANS after receiving ssCAR-T.
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