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

慢性淋巴细胞白血病 医学 细胞因子释放综合征 耐火材料(行星科学) 内科学 CD8型 嵌合抗原受体 白血病 CD19 肿瘤科 淋巴瘤 移植 免疫学 胃肠病学 抗原 T细胞 免疫系统 生物 天体生物学
作者
Patrick Derigs,Maria‐Luisa Schubert,Peter Dreger,Anita Schmitt,Schayan Yousefian,Simon Haas,Caroline Röthemeier,Brigitte Neuber,Angela Hückelhoven‐Krauss,Monika Brüggemann,Helga Bernhard,Guido Kobbe,A. Lindemann,Mathias Rummel,Birgit Michels,Felix Korell,Anthony D. Ho,Carsten Müller‐Tidow,Michael Schmitt
出处
期刊:Leukemia [Springer Nature]
卷期号:38 (11): 2419-2428 被引量:24
标识
DOI:10.1038/s41375-024-02392-7
摘要

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 6 to 200 × 10 6 CART/m 2 . 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.
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