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.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Prediction of severe CRS and determination of biomarkers in B cell-acute lymphoblastic leukemia treated with CAR-T cells.
Prediction of severe CRS and determination of biomarkers in B cell-acute lymphoblastic leukemia treated with CAR-T cells.
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我们的研究将为肿瘤 CAR-T 免疫治疗期间 sCRS 的及时预防和治疗提供重要信息,这对降低患者死亡率至关重要。
通过分析临床因素热图并比较重度与非重度CRS患者,可识别显著差异因素并了解其相互关系。最终采用决策树方法预测儿童和成人sCRS发生时间,纳入同日、前一日及初始值等变量。
研究检测了202例CAR-T 治疗患者的细胞因子和临床生物标志物。CAR-T 输注后,包括IFN-γ、IL-6、IL-10、铁蛋白和D-二聚体在内的25项临床指标峰值均与重度CRS高度相关。采用决策树模型,可利用同日、前一日及初始值三类临床因素,准确预测哪些患者会发生重度CRS。C反应蛋白和铁蛋白等血清生物标志物的变化与CRS相关,但单独不能预测重度CRS发生。
本研究将为肿瘤CAR-T 免疫治疗期间及时预防和处理sCRS提供重要信息,这对于降低患者死亡率至关重要。
By analyzing the heat map of clinical factors and comparing them between severe and non-severe CRS, we can identify significant differences among these factors and understand their interrelationships. Ultimately, a decision tree approach was employed to predict the timing of severe CRS in both children and adults, considering variables such as the same day, the day before, and initial values.
We measured cytokines and clinical biomarkers in 202 patients who received CAR-T therapy. Peak levels of 25 clinical factors, including IFN- , IL6, IL10, ferritin, and D-dimer, were highly associated with severe CRS after CAR T cell infusion. Using the decision tree model, we were able to accurately predict which patients would develop severe CRS consisting of three clinical factors, classified as same-day, day-ahead, and initial value prediction. Changes in serum biomarkers, including C-reactive protein and ferritin, were associated with CRS, but did not alone predict the development of severe CRS.
Our research will provide significant information for the timely prevention and treatment of sCRS, during CAR-T immunotherapy for tumors, which is essential to reduce the mortality rate of patients.
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