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:Cell-Free DNA Dynamic Concentration and Other Variables Are Predictors of Early Progression after Chimeric Antigen Receptor T Cell Therapy in Patients with Diffuse Large B Cell Lymphoma.
Cell-Free DNA Dynamic Concentration and Other Variables Are Predictors of Early Progression after Chimeric Antigen Receptor T Cell Therapy in Patients with Diffuse Large B Cell Lymphoma.
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。
我们提出一种新型生物标志物,可识别嵌合抗原受体(CAR)T细胞治疗后早期进展风险较高的患者。使用单采前(PA)和淋巴细胞清除前(PL)样本计算无细胞DNA(cfDNA),可监测肿瘤动态变化(ΔcfDNA)。本研究评估了58例复发/难治性弥漫大B细胞淋巴瘤(DLBCL)患者的cfDNA、其他生物标志物和临床变量。输注后1个月疾病进展与以下因素高度相关:cfDNA>11 ng/mL血浆(P=0.003)、PL时C反应蛋白(CRP)>1.06 mg/dL(P=0.004)、PL时乳酸脱氢酶(LDH)>304(P=0.006)、PL时疾病状态为进展性疾病(P=0.035)以及男性(P=0.016)。校正cfDNA、PL时CRP和LDH、PL时疾病状态及性别后,cfDNA仍与CAR-T 细胞输注后1个月进展相关。
We propose a novel biomarker that can identify patients at high risk of early progression after chimeric antigen receptor (CAR) T cell therapy. Calculation of cell-free DNA (cfDNA) with a pre-apheresis (PA) and pre-lymphodepletion (PL) sample allows monitoring of tumor dynamics ( cfDNA). In the present study, cfDNA and other biomarkers and clinical variables were evaluated in 58 patients with relapsed/refractory diffuse large B cell lymphoma (DLBCL).
cfDNA (>11 ng/mL plasma; P =. 003), C-reactive protein (CRP) PL (>1. 06 mg/dL; P = . 004), lactate dehydrogenase (LDH) PL (>304; P = . 006), disease status PL (progressive disease; P = . 035) and sex (male; P = . 016) were highly correlated with 1 month progression. After adjusting for cfDNA, CRP PL, and LDH PL, disease status PL, and sex, cfDNA remained associated with 1-month progression after CAR T cell infusion.
MEMBER ACCOUNT
登录成功会直接打开下一页。