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首页> 外文期刊>American Journal of Cancer Research >First-in-man clinical trial of CAR NK-92 cells: safety test of CD33-CAR NK-92 cells in patients with relapsed and refractory acute myeloid leukemia
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First-in-man clinical trial of CAR NK-92 cells: safety test of CD33-CAR NK-92 cells in patients with relapsed and refractory acute myeloid leukemia

机译:CAR NK-92细胞的首次人类临床试验:CD33-CAR NK-92细胞在复发和难治性急性髓细胞性白血病患者中的安全性测试

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摘要

CAR T cells have shown clinical efficacy for acute lymphoblastic leukemia, but this therapy has not been effective for acute myeloid leukemia (AML), and other treatment options are needed. Theoretically, CAR-NK cells have a more favorable toxicity profile compared to CAR T cells, especially in avoiding adverse effects such as cytokine release syndrome. However, the clinical evidence for this has not yet been reported. In the current study, we tested the safety of CD33-CAR NK cells in patients with relapsed and refractory AML. At doses up to 5 × 109 (5 billion) cells per patient, no significant adverse effects were observed. CAR NK-92 cells can be produced at much lower cost compared to CAR T cells, and we believe after being optimized, they will be widely accessible for the treatment of cancer.
机译:CAR T细胞已显示出对急性淋巴细胞白血病的临床疗效,但该疗法对急性髓细胞性白血病(AML)无效,因此需要其他治疗选择。从理论上讲,与CAR T细胞相比,CAR-NK细胞具有更有利的毒性特征,尤其是在避免诸如细胞因子释放综合征等不利影响方面。但是,尚未对此进行临床证明。在本研究中,我们测试了CD33-CAR NK细胞在复发性和难治性AML患者中的安全性。每位患者剂量最高为5×109(50亿)个细胞时,未观察到明显的不良反应。与CAR T细胞相比,CAR NK-92细胞的生产成本低得多,我们相信经过优化后,它们将可广泛用于治疗癌症。

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