[CD19 CAR-T treatment for B-lymphoblastic lymphoma complicated with disseminated intravascular coagulation: a case report and literature review].

Q3 Medicine
Y Y Li, P R Li, H W Jiang, H Mei
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引用次数: 0

Abstract

Objective: To explore the clinical manifestations, pathogenesis, and therapeutic approaches of disseminated intravascular coagulation (DIC) associated with chimeric antigen receptor T-cell (CAR-T) therapy for B-lymphoblastic lymphoma. Methods: Retrospective collection and analysis were conducted on the clinical data of a patient with B-lymphoblastic lymphoma who received CAR-T therapy in the Hematology Department of Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, in April 2020. To review the literatures, Chinese databases (CNKI, Wanfang Database) and PubMed were searched form database inception up to November 2024 using the retrieval entries "chimeric antigen receptor T-cell therapy", "CAR-T", "coagulation", "bleeding", and "thrombosis" . Results: The patient, a 32-year-old male, diagnosed with B-lymphoblastic lymphoma for over 10 months, relapsed after three cycles of chemotherapy and allogeneic hematopoietic stem cell transplantation, with bone marrow cytology indicating 20.24% abnormal phenotype B-lineage precursor cells. After CAR-T cell infusion at a dose of 4×10(6)/kg, the patient developed grade 2 cytokine release syndrome (CRS) on day 2, nasal bleeding on day 4, high fever again on day 9, with worsening coagulation parameters, DIC and persistent hypofibrinogenemia. After treatment with tocilizumab, corticosteroids to counteract CRS, and active replacement therapy such as administration of blood product and fibrinogen, the patient's CRS and coagulation abnormalities gradually improved. The patient was followed up for 16 months regularly after CAR-T therapy, with CAR-T cells sustained and minimal residual disease remained negative as assessed by bone marrow flow cytometry. Subsequently, the patient stopped taking oral immunosuppressants on his own, which aggravated rejection reaction complicated with infection. The patient and his family requested to be discharged and lost the follow-up. A total of 20 relevant English articles and 6 Chinese articles were retrieved from the literature search. Conclusion: CAR-T-associated coagulopathy occurs alongside CRS. It is characterized by hypofibrinogenemia, and is life-threatening when progressing to DIC. Anti-CRS and replacement therapies have proven to be effective treatment strategies.

[CD19 CAR-T治疗b淋巴母细胞淋巴瘤合并弥散性血管内凝血1例报告及文献复习]。
目的:探讨嵌合抗原受体t细胞(CAR-T)治疗b淋巴母细胞淋巴瘤并发弥散性血管内凝血(DIC)的临床表现、发病机制及治疗方法。方法:回顾性收集和分析华中科技大学同济医学院协和医院血液科于2020年4月接受CAR-T治疗的1例b淋巴母细胞淋巴瘤患者的临床资料。为了检索相关文献,我们从中国知网(CNKI)、万方数据库(Wanfang Database)和PubMed数据库(PubMed)检索自建库至2024年11月,检索条目为“嵌合抗原受体t细胞疗法”、“CAR-T”、“凝血”、“出血”和“血栓形成”。结果:患者男性,32岁,诊断为b淋巴母细胞淋巴瘤10个多月,经3个周期化疗和异基因造血干细胞移植后复发,骨髓细胞学显示20.24%表型b系前体细胞异常。CAR-T细胞输注4×10(6)/kg剂量后,患者第2天出现2级细胞因子释放综合征(CRS),第4天出现鼻出血,第9天再次出现高热,凝血参数恶化,DIC和持续性低纤维蛋白原血症。经托珠单抗、皮质类固醇抗CRS及主动替代治疗(如给予血液制品和纤维蛋白原)治疗后,患者的CRS和凝血异常逐渐改善。在CAR-T治疗后,患者定期随访16个月,通过骨髓流式细胞术评估,CAR-T细胞持续存在,最小残留疾病为阴性。随后患者自行停止口服免疫抑制剂,加重了排斥反应并发感染。患者及家属要求出院,失访。从文献检索中共检索到相关英文文章20篇,中文文章6篇。结论:car - t相关凝血功能障碍与CRS同时发生。它的特点是低纤维蛋白原血症,当进展为DIC时是危及生命的。抗crs和替代疗法已被证明是有效的治疗策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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CiteScore
0.80
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