医学
环磷酰胺
内科学
细胞因子释放综合征
痹症科
免疫学
CD19
免疫系统
自身免疫性疾病
临床试验
结缔组织病
抗原
硬皮病(真菌)
皮肌炎
全身性疾病
免疫疗法
血液学
免疫病理学
抗体
红斑狼疮
间质性肺病
美罗华
系统性硬皮病
临床研究阶段
胃肠病学
肌炎
作者
Fabian Müller,Melanie Hagen,Andreas Wirsching,Soraya Kharboutli,Michael Aigner,Simon Völkl,Sascha Kretschmann,Koray Tascilar,Jule Taubmann,Laura Bucci,Maria Gabriella Raimondo,Christina Bergmann,Tobias Rothe,Giulia Corte,Carlo Tur,Luis Muñoz,Sebastian Böltz,Louis Schuster,F Hartmann,Panagiotis Garantziotis
出处
期刊:Nature Medicine
[Nature Portfolio]
日期:2026-01-07
卷期号:32 (3): 1142-1151
被引量:25
标识
DOI:10.1038/s41591-025-04185-6
摘要
Chimeric antigen receptor (CAR)-T cells are considered a powerful therapeutic tool to reset the immune system in patients with autoimmune diseases. Innovative trial designs are needed to allow feasible testing of the safety and efficacy of CAR-T cells in clinical studies. CASTLE (CAR-T cells in systemic B cell mediated autoimmune disease) is a phase 1/2a two-stage optimal design basket study that investigated the safety and efficacy of zorpocabtagene autoleucel (Zorpo-cel, also known as MB-CART19.1), an autologous CD19 CAR-T cell product, in patients with treatment-resistant systemic lupus erythematosus (SLE), systemic sclerosis (SSc) and idiopathic inflammatory myopathies (IIM). The primary safety outcome was the rate of cytokine release syndrome (CRS) and immune effector cell-associated neurotoxicity syndrome (ICANS). The secondary clinical efficacy outcomes were remission of SLE according to DORIS criteria, no progression of interstitial lung disease in SSc and American College of Rheumatology (ACR) major/moderate response in IIM after 24 weeks. A total of 24 patients were enrolled (10 with SLE, 9 with SSc and 5 with IIM), all receiving a single infusion of Zorpo-cel after stopping immunosuppressive treatments and receiving standard lymphodepletion with cyclophosphamide and fludarabine. Primary and secondary endpoints of CASTLE were met. Regarding safety, no CRS higher than grade 2 and no ICANS occurred. Regarding efficacy, 22 of the 24 patients achieved predefined efficacy endpoints, with 9 out of 10 patients with SLE reaching DORIS remission, 9 out of 9 patients with SSc showing no disease progression, and 4 out of 5 patients with IIM reaching ACR major/moderate response. Furthermore, all patients remained free of glucocorticoids and any other immunosuppressive treatment over the entire observation period of 24 weeks. CASTLE suggests the feasibility, safety and efficacy of Zorpo-cel in three different autoimmune diseases and paves the way for conducting a pivotal study. ClinicalTrials.gov identifier: NCT06347718 , EudraCT identifier: 2022-001366-35 .
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