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]
日期:2024-08-27
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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