[BCMA/CS1 bispecific CAR-T cell therapy for multiple myeloma complicated with thrombocytopenia: a case report and literature review].

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

Abstract

Objective: To investigate the clinical manifestations, diagnostic and therapeutic strategies, for thrombocytopenia after BCMA/CS1 bispecific chimeric antigen receptor T-cell (CAR-T cell) therapy in patients with multiple myeloma. Methods: Retrospective collection and analysis were conducted on the clinical data of a patient with multiple myeloma who received BCMA/CS1 bispecific CAR-T cell therapy in the Hematology Department of Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, in June 2021. To review the literature, Chinese databases (CNKI, Wanfang Database) and PubMed were searched from their inception up to November 2024 using the keywords "chimeric antigen receptor T-cell therapy", "thrombocytopenia", "CAR-T", "BCMA", and "CS1" . Results: A 72-year-old male patient was diagnosed with light chain κ-type multiple myeloma (R-ISS stage Ⅱ) in a local hospital and had a prolonged treatment course with poor disease control despite multiple adjustments of chemotherapy regimens. The patient met the inclusion criteria for the BCMA/CS1 dual-target CAR-T cell clinical trial (NCT04662099) and achieved complete remission two months after receiving a low dose of CAR-T cells. On the 8th day after CAR-T cell infusion, the patient developed grade 3 cytokine release syndrome, followed by severe gastrointestinal bleeding and persistent grade ≥3 thrombocytopenia, accompanied by a significant increase in thrombopoietin levels, with no megakaryocytes observed in bone marrow cytology. After treatment with rituximab, significant improvement was observed with platelet count gradually increased. However, the patient experienced persistent malnutrition and cachexia, and transferred to the gastroenterology department, after which follow-up was lost. A total of 24 relevant English articles and 8 Chinese articles were retrieved from the literature search. Conclusion: CAR-T cell therapy associated thrombocytopenia is characterized by thrombocytopenia and megakaryocyte production disorders. Persistent thrombocytopenia increases the risk of bleeding, and the use of CD20 monoclonal antibodies and supportive therapy can effectively improve thrombocytopenia.

[BCMA/CS1双特异性CAR-T细胞治疗多发性骨髓瘤合并血小板减少1例报告及文献复习]。
目的:探讨多发性骨髓瘤患者接受BCMA/CS1双特异性嵌合抗原受体t细胞(CAR-T细胞)治疗后血小板减少症的临床表现、诊断和治疗策略。方法:回顾性收集和分析2021年6月华中科技大学同济医学院协和医院血液科接受BCMA/CS1双特异性CAR-T细胞治疗的1例多发性骨髓瘤患者的临床资料。检索中文数据库(中国知网、万方数据库)和PubMed数据库,检索关键词为“嵌合抗原受体t细胞疗法”、“血小板减少症”、“CAR-T”、“BCMA”和“CS1”,检索时间截止到2024年11月。结果:一名72岁男性患者在当地医院确诊为轻链κ型多发性骨髓瘤(R-ISS期Ⅱ),经多次调整化疗方案,疗程延长,病情控制不佳。该患者符合BCMA/CS1双靶点CAR-T细胞临床试验(NCT04662099)的纳入标准,并在接受低剂量CAR-T细胞治疗两个月后实现完全缓解。CAR-T细胞输注后第8天,患者出现3级细胞因子释放综合征,随后出现严重胃肠道出血和持续性≥3级血小板减少症,伴血小板生成素水平显著升高,骨髓细胞学未见巨核细胞。经利妥昔单抗治疗后,血小板计数逐渐升高,明显改善。然而,患者经历了持续的营养不良和恶病质,并转移到消化内科,之后失去了随访。从文献检索中共检索到相关英文文献24篇,中文文献8篇。结论:CAR-T细胞治疗相关的血小板减少以血小板减少和巨核细胞产生障碍为特征。持续性血小板减少增加出血风险,使用CD20单克隆抗体和支持治疗可有效改善血小板减少。
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
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