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用于复发/难治性慢性淋巴细胞白血病的第三代抗 CD19 CAR T 细胞:一项 1/2 期研究。

Third-generation anti-CD19 CAR T cells for relapsed/refractory chronic lymphocytic leukemia: a phase 1/2 study.

机构信息

Internal Medicine V, Hematology, Oncology and Rheumatology, Heidelberg University Hospital, Heidelberg, Germany.

Berlin Institute of Health (BIH) at Charité - Universitätsmedizin Berlin, Berlin, Germany.

出版信息

Leukemia. 2024 Nov;38(11):2419-2428. doi: 10.1038/s41375-024-02392-7. Epub 2024 Aug 27.

Abstract

Third-generation chimeric antigen receptor T cells (CARTs) for relapsed or refractory (r/r) chronic lymphocytic leukemia (CLL) may improve efficacy compared to second-generation CARTs due to their enhanced CAR design. We performed the first phase 1/2 investigator-initiated trial evaluating escalating doses of third-generation CARTs (HD-CAR-1) targeting CD19 in patients with r/r CLL and B-cell lymphoma. CLL eligibility criteria were failure to two therapy lines including at least one pathway inhibitor and/or allogeneic hematopoietic cell transplantation. Nine heavily pretreated patients received HD-CAR-1 at dose levels ranging from 1 × 10 to 200 × 10 CART/m. In-house HD-CAR-1 manufacturing was successful for all patients. While neurotoxicity was absent, one case of grade 3 cytokine release syndrome was observed. By day 90, six patients (67%) attained a CR, five of these (83%) with undetectable MRD. With a median follow-up of 27 months, 2-year PFS and OS were 30% and 69%, respectively. HD-CAR-1 products of responders contained significantly more CD4 + T cells compared to non-responders. In non-responders, a strong enrichment of effector memory-like CD8 + T cells with high expression of CD39 and/or CD197 was observed. HD-CAR-1 demonstrated encouraging efficacy and exceptionally low treatment-specific toxicity, presenting new treatment options for patients with r/r CLL. Trial registration: #NCT03676504.

摘要

第三代嵌合抗原受体 T 细胞(CART)治疗复发或难治性(r/r)慢性淋巴细胞白血病(CLL)可能比第二代 CART 更有效,因为其 CAR 设计得到了增强。我们进行了首例由研究者发起的 1/2 期临床试验,评估了靶向 CD19 的第三代 CART(HD-CAR-1)在 r/r CLL 和 B 细胞淋巴瘤患者中的递增剂量。CLL 的入选标准为在至少接受两种治疗方案(包括至少一种通路抑制剂和/或异基因造血细胞移植)后疾病进展。9 例预处理较多的患者接受了 1×10 至 200×10 CART/m 的剂量水平的 HD-CAR-1 治疗。所有患者的内部 HD-CAR-1 制造均成功。虽然没有出现神经毒性,但观察到 1 例 3 级细胞因子释放综合征。在第 90 天,6 例患者(67%)达到完全缓解,其中 5 例(83%)未检测到微小残留病灶。中位随访 27 个月后,2 年 PFS 和 OS 分别为 30%和 69%。与无应答者相比,应答者的 HD-CAR-1 产品中 CD4+T 细胞明显更多。在无应答者中,观察到具有高表达 CD39 和/或 CD197 的效应记忆样 CD8+T 细胞强烈富集。HD-CAR-1 表现出令人鼓舞的疗效和极低的治疗特异性毒性,为 r/r CLL 患者提供了新的治疗选择。试验注册:#NCT03676504。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d35/11519001/a86577b388ab/41375_2024_2392_Fig1_HTML.jpg

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