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:Added prognostic value of baseline pre-infusion (18)F-FDG PET/CT in diffuse large B-cell lymphoma patients receiving chimeric antigen receptor T-cell therapy.
Added prognostic value of baseline pre-infusion (18)F-FDG PET/CT in diffuse large B-cell lymphoma patients receiving chimeric antigen receptor T-cell therapy.
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在这项经研究伦理委员会批准的回顾性研究中,我们评估了输注前[18F]FDG PET/CT对接受嵌合抗原T细胞(CAR-T)治疗的复发/难治性弥漫大B细胞淋巴瘤(DLBCL)患者的预后价值。共回顾了2018年至2023年间接受CAR-T 治疗的159例患者。Deauville评分4分和5分被认为基线存在显著残留病灶。计算了标准化摄取值(SUV)、全身代谢肿瘤体积(MTV)和总病灶糖酵解(TLG)。
此外,测量了全身肿瘤病灶之间的最远距离(Dmax)以及距脾脏的距离(spleen Dmax)。生存分析评估了临床和影像学衍生变量对无进展生存期(PFS)和总生存期(OS)预后的预测价值。在129例接受输注前[18F]FDG PET/CT的DLBCL患者中,117/129(91%)存在显著残留病灶。CAR-T 治疗后中位PFS和OS分别为六个月和九个月。对于PFS,在多变量分析中仍保持显著的变量为血清LDH(HR = 1.68)和TLG(HR = 4.31),二者是PFS的独立预测因子。对于OS,在多变量分析中唯一保持显著性的变量是[18F]FDG PET/CT衍生的标准化Dmax(HR = 3.28)。输注前[18F]FDG PET/CT可为CAR-T 候选患者提供有价值的预后信息,改善患者管理。
In this Research Ethics Board-approved retrospective study, we evaluated pre-infusion [ 18 F]FDG PET/CT prognostic value in relapsed/refractory diffuse large B-cell lymphoma (DLBCL) patients undergoing chimeric antigen T-cell (CAR-T) therapy. A total of 159 Patients treated with CAR-T between 2018 and 2023 were reviewed. Deauville scores 4 and 5 were considered to be a significant residual disease at baseline. Standardized uptake values (SUVs), whole-body metabolic tumour volume (MTV) and total lesion glycolysis (TLG) were calculated.
Additionally, the furthest distance between tumoral lesions throughout the body (Dmax) and from the spleen (spleen Dmax) were measured. Survival analyses evaluated the predictive value of the clinical and imaging-derived variables for progression-free survival (PFS) and overall survival (OS) prognostication. Of 129 DLBCL patients with pre-infusion [ 18 F]FDG PET/CT, 117/129 (91%) had significant residual disease. The median PFS and OS post-CAR-T were six and nine months, respectively.
For PFS, variables that remained significant in the multivariate analysis were serum LDH (HR = 1. 68) and TLG (HR = 4. 31), being independent predictors of PFS. Considering OS, the only variable which retained its significance in the multivariate analysis was [ 18 F]FDG PET/CT-derived standardized Dmax (HR = 3. 28). Pre-infusion [ 18 F]FDG PET/CT can provide valuable prognostic information in CAR-T candidates, enhancing patient management.
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