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病例报告:多发性骨髓瘤患者 CAR-T 细胞治疗后的 ITP 治疗

英文原题:Case Report: ITP Treatment After CAR-T Cell Therapy in Patients With Multiple Myeloma.

查看英文原题

Case Report: ITP Treatment After CAR-T Cell Therapy in Patients With Multiple Myeloma.

PubMed 2022/06/16(内容时间) Front Immunol Q1 · IF 7(JCR 2025)

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中文摘要

CAR-T(CAR-T)细胞疗法是复发/难治性血液恶性肿瘤(包括多发性骨髓瘤[MM])患者的有吸引力治疗策略。工程化T细胞可攻击表达肿瘤相关抗原的恶性细胞,从而提高疗效。但细胞因子释放综合征(CRS)、免疫效应细胞相关神经毒性综合征(ICANS)和血液学毒性仍是CAR-T 治疗挑战。其中,血液学毒性(包括血小板减少)对部分患者影响持续时间较长,治疗前后均可延续。本文报告3例复发/难治性MM患者在接受双特异性CAR-T 治疗后出现难治性血小板减少,伴血小板自身抗体阳性和血浆血小板生成素(TPO)浓度升高;患者经免疫性血小板减少症(ITP)标准治疗后均成功改善。目前尚无明确发病机制或治疗指南,这些病例可为CAR-T 治疗后血小板减少的处理提供参考,并推动探索其潜在病理生理机制。

展开英文摘要原文

Chimeric antigen receptor T (CAR-T) cell therapy is an attractive strategy for patients with relapsed or refractory hematological malignancies including multiple myeloma (MM). T cells are engineered to attack malignant cells that express tumor-associated antigens and better efficacy could be achieved.

However, cytokine release syndrome (CRS), immune effector cell-associated neurotoxicity syndrome (ICANS), and hematologic toxicity are still challenges for CAR-T cell therapy. Among them, hematologic toxicity including thrombocytopenia has a longer duration and lasting effect during and after the treatment for some patients.

Here, we present 3 cases of hematologic toxicity manifested as refractory thrombocytopenia with platelet autoantibodies positive and plasma thrombopoietin (TPO) concentration elevated after bispecific CAR-T cell therapy in relapsed/refractory (R/R) MM patients who were successfully treated with standard therapy of immune thrombocytopenia (ITP).

Without clear pathogenesis or guidance on therapy published, our cases provide a reference for the treatment of thrombocytopenia after CAR-T cell therapy and inspire exploration of the underlying pathophysiological mechanisms.

论文信息

作者
Du M、Huang L、Kou H、Li C、Hu Y、Mei H
单位
Institute of Hematology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.China
文献类型
病例报告 · 非美国政府资助研究
期刊
Frontiers in immunology2022
原文标识
PubMed 35784357 · DOI 10.3389/fimmu.2022.898341