CAR-T(CAR-T)细胞疗法在非肿瘤性疾病中的应用
Chimeric antigen receptor T (CAR-T) cell therapy in non-oncological diseases.
CAR-T(CAR-T)细胞在血液系统恶性肿瘤中的应用推动了这种免疫治疗形式的显著进展。
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Case Report: ITP Treatment After CAR-T Cell Therapy in Patients With Multiple Myeloma.
Case Report: ITP Treatment After CAR-T Cell Therapy in Patients With Multiple Myeloma.
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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。
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.
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