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:Prognostic value of early post-treatment (18)F-FDG PET/CT in diffuse large B-cell lymphoma patients receiving chimeric antigen receptor T-cell therapy.
Prognostic value of early post-treatment (18)F-FDG PET/CT in diffuse large B-cell lymphoma patients receiving chimeric antigen receptor T-cell therapy.
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治疗后早期 18F-FDG PET/CT 可为接受 CAR-T 治疗的弥漫大 B 细胞淋巴瘤患者提供有价值的预后信息。
评估CAR-T 细胞治疗弥漫性大B细胞淋巴瘤(DLBCL)患者早期治疗后18F-FDG PET/CT的预后价值。
本回顾性研究纳入2018年1月至2023年5月CAR-T 治疗前接受影像学检查的159例患者,其中51例同时完成输注前基线和治疗后1个月18F-FDG PET/CT。提取PET/CT参数,包括标准摄取值(SUV)、代谢肿瘤体积(MTV)、总病灶糖酵解(TLG)和Dmax,并计算相对基线的变化值。记录进展或死亡时间。采用Kaplan-Meier法单变量分析无进展生存期(PFS)和总生存期(OS),采用Mantel-Cox log-rank检验评估差异显著性;显著参数纳入多变量Cox回归。
共51例患者入组,平均年龄56岁。所有患者基线Deauville评分均为4分(51例中14例,28%)或5分(37例,72%)。治疗1个月时,28%的患者达到完全代谢缓解,72%仍有18F-FDG高摄取的显著残留病灶。在有残留病灶的患者中,治疗后1个月扫描的SUVmax、SUVpeak、SUVmax/肝脏比值和MTV均显著降低。PFS多变量分析纳入血清LDH、治疗后1个月SUVmax/肝脏比值、治疗后1个月TLG及基线Dmax。治疗后1个月SUVmax/肝脏比值(HR=5.21;P=0.004)和基线Dmax(HR=13.8;P=0.013)仍具有显著性,是PFS的独立预测因素。OS多变量分析纳入血清LDH、SUVmean/肝脏比值变化、TLG百分比变化及治疗后1个月Dmax。TLG百分比变化仍显著,是OS的独立预测因素(HR=4.37;P=0.023)。
早期治疗后18F-FDG PET/CT可为接受CAR-T 治疗的DLBCL患者提供有价值的预后信息。最重要的结局预测因素包括基线疾病范围、治疗后1个月的代谢活性及相对基线代谢肿瘤负荷变化。
To evaluate the prognostic value of early post-treatment 18 F-FDG PET/CT in diffuse large B-cell lymphoma (DLBCL) patients undergoing chimeric antigen receptor T-cell (CAR-T) therapy.
In this retrospective study, 159 patients referred for imaging prior to CAR-T therapy between January 2018 and May 2023 were reviewed. Of those, 51 with both baseline pre-infusion and one-month post-treatment 18 F-FDG PET/CTs were included. 18 F-FDG PET/CT parameters were derived, including standard uptake values (SUVs), metabolic tumour volume (MTV), total lesion glycolysis (TLG), and Dmax. Additionally, the delta changes from the baseline were calculated. Time to progression/death was documented. For progression-free survival (PFS) and overall survival (OS), univariate analysis was performed using the Kaplan-Meier method. The significance of the difference was measured using the Mantel-Cox log-rank test. Significant parameters entered the multiple Cox regression.
Overall, 51 patients (mean age = 56y) entered the study. All had Deauville scores of 4 (14/51; 28%) or 5 (37/51; 72%) at baseline. At one month, 28% of patients showed a complete metabolic response, while 72% had 18 F-FDG-avid significant residual disease. Investigating those with residual disease, SUVmax, SUVpeak, SUVmax-to-Liver ratio and MTV were significantly lower in the one-month post-treatment scan. For PFS evaluation, serum LDH, one-month post-treatment SUVmax-to-liver ratio, one-month post-treatment TLG, and baseline Dmax entered the multivariate analysis. The one-month post-treatment SUVmax-to-liver ratio (Hazard ratio [HR] = 5.21; p = 0.004) and baseline Dmax (HR = 13.8; p = 0.013) retained significance, being independent predictors of PFS. For OS, serum LDH, delta SUVmean-to-liver ratio, delta percentage TLG, and one-month post-treatment Dmax were included in the multivariate analysis. The delta percentage TLG (HR = 4.37; p = 0.023) remained significant as an independent predictor of OS.
Early post-treatment 18 F-FDG PET/CT can provide valuable prognostic information for DLBCL patients receiving CAR-T. The most significant predictors of outcomes would be the baseline extent of the disease, one-month post-treatment avidity, and changes in the metabolic burden from baseline.
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