CAR-T(CAR-T)细胞疗法在非肿瘤性疾病中的应用
Chimeric antigen receptor T (CAR-T) cell therapy in non-oncological diseases.
CAR-T(CAR-T)细胞在血液系统恶性肿瘤中的应用推动了这种免疫治疗形式的显著进展。
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:CD19-directed CAR T-cell therapy for treatment of primary CNS lymphoma.
CD19-directed CAR T-cell therapy for treatment of primary CNS lymphoma.
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CD19靶向嵌合抗原受体(CD19CAR)T细胞疗法在治疗多种B细胞系恶性肿瘤方面已取得成功,包括B细胞非霍奇金淋巴瘤(NHL)。由于对潜在毒性的担忧,该治疗模式尚未扩展至中枢神经系统(CNS)表现的NHL。静脉注射的CD19CAR-T 细胞可在脑脊液(CSF)中检测到,提示嵌合抗原受体(CAR)T细胞能够从外周迁移至CNS,并可能在那里介导抗淋巴瘤活性。
在此,我们报告了在我们正在进行的1期临床试验中接受CD19CAR-T 细胞治疗的原发性CNS淋巴瘤(PCNSL;n = 5)患者亚群的结果。所有患者在CAR-T 细胞输注后均发生1级细胞因子释放综合征和神经毒性;毒性可逆且可耐受,无治疗相关死亡。在初始疾病缓解时,5例患者中有3例(60%;90%置信区间,19-92%)似乎达到完全缓解,表现为脑部强化病灶消退;其余2例患者疾病稳定。尽管研究队列较小,我们证明使用CD19CAR-T 细胞治疗PCNSL是安全且可行的。该试验注册于www.ClinicalTrials.gov,编号为#NCT02153580。
CD19-directed chimeric antigen receptor (CD19CAR) T-cell therapy has been successful in treating several B-cell lineage malignancies, including B-cell non-Hodgkin lymphoma (NHL). This modality has not yet been extended to NHL manifesting in the central nervous system (CNS), primarily as a result of concerns for potential toxicity.
CD19CAR T cells administered IV are detectable in cerebrospinal fluid (CSF), suggesting that chimeric antigen receptor (CAR) T cells can migrate from the periphery into the CNS, where they can potentially mediate antilymphoma activity.
Here, we report the outcome of a subset of patients with primary CNS lymphoma (PCNSL; n = 5) who were treated with CD19CAR T cells in our ongoing phase 1 clinical trial. All patients developed grade 1 cytokine release syndrome and neurotoxicity post-CAR T-cell infusion; toxicities were reversible and tolerable, and there were no treatment-related deaths.
At initial disease response, 3 of 5 patients (60%; 90% confidence interval, 19-92%) seemed to achieve complete remission, as indicated by resolution of enhancing brain lesions; the remaining 2 patients had stable disease. Although the study cohort was small, we demonstrate that using CD19CAR T cells to treat PCNSL can be safe and feasible. This trial was registered at www. clinicaltrials. gov as #NCT02153580.
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