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CD7 CAR-T 细胞用于复发或难治性 CD7 阳性急性髓系白血病患者

英文原题:CD7 chimeric antigen receptor T cells in patients with relapsed or refractory CD7-positive acute myeloid leukemia.

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CD7 chimeric antigen receptor T cells in patients with relapsed or refractory CD7-positive acute myeloid leukemia.

PubMed 2026/07/03(内容时间) Leukemia Q1 · IF 8.8(JCR 2025)

研究概要

CD7在约30%的AML病例中表达,是一个有前景的靶点。

中文摘要

尽管 CAR-T 细胞疗法已经彻底改变了血液系统恶性肿瘤的治疗,但其在急性髓系白血病中的应用仍然具有挑战性。CD7 在大约 30% 的 AML 病例中表达,是一个有前景的靶点。这项 I 期临床试验(NCT04599556)评估了 CD7 靶向 CAR-T 细胞疗法在复发/难治性 CD7 阳性 AML 患者中的疗效。患者接受单次自体或供者来源 CD7 CAR-T 细胞输注,采用标准 3 + 3 剂量递增设计,设两个剂量水平。主要终点是剂量限制性毒性的发生率。共入组 14 例患者。治疗相关不良事件包括细胞因子释放综合征(92.9%)、3-4 级血细胞减少(100%)、1 级神经毒性(7.1%)和病毒再激活(78.6%)。客观缓解率为 92.3%,MRD 阴性率为 84.6%。尽管初始有缓解,7 例患者以 CD7 阴性疾病复发。在中位随访 172.5 天时,5 例患者仍处于缓解状态。3 年总生存率和无白血病生存率分别为 34.3% 和 34.1%。这些初步结果表明,CD7 CAR-T 细胞疗法在 R/R AML 患者中具有可控的安全性特征和初步疗效,支持在更大规模试验中进一步研究。

展开英文摘要原文

Although CAR-T cell therapy has revolutionized treatment for hematologic malignancies, its application in acute myeloid leukemia remains challenging. CD7 is expressed in approximately 30% of AML cases and represents a promising target. This phase I clinical trial (NCT04599556) evaluated CD7-targeted CAR-T cell therapy in patients with relapsed/refractory CD7-positive AML. Patients received a single infusion of autologous or donor-derived CD7 CAR-T cells using a standard 3 + 3 dose escalation design across two dose levels. The primary endpoint was the incidence of dose-limiting toxicities. Fourteen patients were enrolled. Treatment-related adverse events included cytokine release syndrome (92.9%), grade 3-4 cytopenia (100%), grade 1 neurotoxicity (7.1%), and viral reactivation (78.6%). The objective response rate was 92.3%, with an MRD-negative rate of 84.6%. Despite initial responses, seven patients relapsed with CD7-negative disease. At a median follow-up of 172.5 days, five patients remained in remission. The 3-year overall survival and leukemia-free survival rates were 34.3% and 34.1%, respectively. These initial results indicate that CD7 CAR-T cell therapy exhibits a manageable safety profile and preliminary efficacy in R/R AML patients, supporting further investigation in larger trials.

论文信息

作者
Zhang M、Liu L、Fu S、Feng J、Zheng H、Wei G、Hong R、Zhao H
第一作者单位
Bone Marrow Transplantation Center, the First Affiliated Hospital, and Liangzhu Laboratory, Zhejiang University School of Medicine, Hangzhou, China.China
通讯作者单位
Bone Marrow Transplantation Center, the First Affiliated Hospital, and Liangzhu Laboratory, Zhejiang University School of Medicine, Hangzhou, China. 1313016@zju.edu.cn.China
文献类型
I 期临床试验
期刊
Leukemia2026 Sep
原文标识
PubMed 42399624 · DOI 10.1038/s41375-026-03017-x