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:Assessment and predictive ability of the absolute neutrophil count in peripheral blood for in vivo CAR T cells expansion and CRS.
Assessment and predictive ability of the absolute neutrophil count in peripheral blood for in vivo CAR T cells expansion and CRS.
分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。
因此,我们提出 ANC 可作为 CAR-T 细胞治疗过程中 CAR 扩增与 CRS 的评估及预测生物标志物,有助于最大化临床疗效、降低治疗相关毒性并延长生存期。
嵌合抗原受体(CAR)T细胞疗法是治疗复发/难治性B细胞恶性肿瘤的先进且有效的免疫疗法。CAR-T 细胞在体内大量扩增并持续发挥抗肿瘤活性,提示治疗应答持久。但该疗法相关不良事件发生率较高,例如细胞因子释放综合征(CRS),会影响疗效,甚至危及生命。目前已有多种输注CAR-T 后与临床应答及毒性相关的标志物被报道。这些生物标志物可有效反映CAR-T 扩增及CRS,但无法预测CAR-T 扩增速率。因此亟需进一步研究以寻找新的生物标志物。
我们分析了两项临床试验中45例B细胞恶性肿瘤患者的绝对中性粒细胞计数(ANC)与CAR扩增及CRS之间的关联。我们提出ANC可能是评估CAR-T 细胞扩增及CRS的实用生物标志物,并分析其预测能力的可行性。
研究纳入17例接受抗B细胞成熟抗原CAR治疗的B细胞血液系统恶性肿瘤患者,以及28例接受CAR19/22 T细胞治疗的患者,并根据ANC是否缺失分组。结果显示,ANC缺失与CAR扩增及扩增速率呈正相关。ANC可作为预测CAR-T 细胞扩增的标志物。此外,ANC缺失患者发生的CRS更严重,且ANC对CRS也具有预测能力。ANC缺失患者血清中多种参与CRS的细胞因子峰值浓度更高。
因此,我们建议将ANC作为CAR-T 治疗期间评估和预测CAR扩增及CRS的生物标志物,以帮助最大化临床疗效、降低治疗相关毒性并延长生存。
Chimeric antigen receptor (CAR) T cell therapy is an advanced and effective immunotherapy for relapsed or refractory B-cell malignancies. High expansion of CAR T cells in vivo and durable antitumor activity indicate a persistent therapeutic response. However, this treatment is linked to a high frequency of adverse events, such as cytokine release syndrome (CRS), which affects its efficacy and can even be life-threatening. At present, a variety of markers associated with clinical response and treatment toxicity after CAR T cells infusion have been reported. Although these biomarkers can act as effective indicators reflecting CAR T cells expansion as well as CRS, they fail to predict the expansion rate of CAR T cells. Hence, further investigation is urgent to find a new biomarker to fill this void.
We analyzed the association between the absolute neutrophil count (ANC) and CAR expansion and CRS in 45 patients with B-cell malignancies from two clinical trials. We proposed that ANC could be a practical biomarker for CAR T cells expansion and CRS, and conducted a feasibility analysis on its predictive ability.
In this study, 17 B-cell hematological malignancy patients with anti-B-cell maturation antigen CAR-treated and 28 with CAR19/22 T-cell-treated were enrolled and divided into an ANC-absence group and an ANC-presence group. The results showed that ANC absence correlated positively with CAR expansion and the expansion rate. The ANC can be used as a predictive marker for CAR T cells expansion. Moreover, the patients with ANC absence experienced a more severe CRS, and ANC performed a predictive ability for CRS. In addition, the peak serum concentration of several cytokines involved in CRS was higher in patients with ANC absence.
Thus, we suggest ANC as an evaluative and predictive biomarker for CAR expansion and CRS during CAR T cell therapy, which can help to maximize clinical efficacy, reduce treatment-related toxicity and prolong survival.
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