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CAR-T 细胞治疗后细胞因子释放综合征合并横纹肌溶解:一例病例报告

英文原题:Cytokine release syndrome complicated with rhabdomyolysis after chimeric antigen receptor T-cell therapy: A case report.

查看英文原题

Cytokine release syndrome complicated with rhabdomyolysis after chimeric antigen receptor T-cell therapy: A case report.

PubMed 2022/09/16(内容时间) World J Clin Cases

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研究概要

肌痛是 CAR-T 治疗后重度 CRS 中一个容易被忽视的症状。

中文摘要

嵌合抗原受体(CAR)T细胞疗法是治疗血液系统恶性肿瘤的有效新方法。细胞因子释放综合征(CRS)和神经毒性是主要毒性。既往尚未报告CAR-T 治疗后CRS诱发横纹肌溶解(RM)的病例。病例摘要:我们报告一例22岁复发性急性淋巴细胞白血病女性患者,先后接受CD19和CD22 CAR-T 细胞输注。患者发生3级CRS并伴RM、需静脉补液的轻度低血压以及轻度低氧,经IL-6受体拮抗剂托珠单抗有效控制。患者未出现免疫效应细胞相关神经毒性综合征体征。CAR-T 治疗后30天再分期扫描显示完全缓解,肌无力症状经康复治疗后改善。

肌痛是CAR-T 治疗后重度CRS中容易被忽略的症状。患者出现肌痛或急性肾功能不全时,有必要监测肌红蛋白水平。

展开英文摘要原文

Chimeric antigen receptor T-Cell (CAR-T) therapy is an effective new treatment for hematologic malignancies. Cytokine release syndrome (CRS) and neurologic toxicity are main toxicities. CRS-induced rhabdomyolysis (RM) followed by CAR-T therapy treatment has not been previously reported. CASE SUMMARY: We report a case of a 22-year-old woman with relapsed acute lymphoblastic leukemia obtained sequential cluster of differentiation (CD) 19 and CD22 CAR-T infusion. This patient experienced grade 3 CRS with RM, mild hypotension requiring intravenous fluids, and mild hypoxia and was managed effectively with the IL-6 receptor antagonist tocilizumab. This patient had no signs of immune effector cell-associated neurologic syndrome. Restaging scans 30 d postCAR-T therapy demonstrated a complete remission, and the symptoms of muscle weakness improved through rehabilitation.

Myalgia is an easily overlooked symptom of severe CRS after CAR-T therapy. It is necessary to monitor myoglobin levels when a patient presents with symptoms of myalgia or acute renal insufficiency.

论文信息

作者
Zhang L、Chen W、Wang XM、Zhang SQ
单位
Department of Hematology, The First Hospital of Shanxi Medical University, Taiyuan 030001, Shanxi Province, China. qiqi994@sina.com.China
文献类型
病例报告
期刊
World journal of clinical cases2022 Sep 16
原文标识
PubMed 36159401 · DOI 10.12998/wjcc.v10.i26.9398