Prognostic value of early post-treatment 18F-FDG PET/CT in diffuse large B-cell lymphoma patients receiving chimeric antigen receptor T-cell therapy.

IF 3.5 2区 医学 Q2 ONCOLOGY
Seyed Ali Mirshahvalad, Andres Kohan, Roshini Kulanthaivelu, Claudia Ortega, Ur Metser, David Hodgson, Robert Kridel, Christine Chen, Sita Bhella, Kelly Yuen Wai Chin, Patrick Veit-Haibach
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引用次数: 0

Abstract

Purpose: To evaluate the prognostic value of early post-treatment 18F-FDG PET/CT in diffuse large B-cell lymphoma (DLBCL) patients undergoing chimeric antigen receptor T-cell (CAR-T) therapy.

Methods: 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 18F-FDG PET/CTs were included. 18F-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.

Results: 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 18F-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.

Conclusion: Early post-treatment 18F-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.

Abstract Image

Abstract Image

Abstract Image

18F-FDG PET/CT对接受嵌合抗原受体t细胞治疗的弥漫性大b细胞淋巴瘤患者的预后价值
目的:探讨18F-FDG PET/CT在弥漫性大b细胞淋巴瘤(DLBCL)患者接受CAR-T治疗后早期的预后价值。方法:在这项回顾性研究中,对2018年1月至2023年5月期间接受CAR-T治疗前影像学检查的159例患者进行了回顾。其中,51例同时进行基线输注前和治疗后1个月的18F-FDG PET/ ct检查。导出18F-FDG PET/CT参数,包括标准摄取值(suv)、代谢肿瘤体积(MTV)、病变总糖酵解(TLG)和Dmax。此外,还计算了与基线相比的增量变化。记录了进展/死亡的时间。对于无进展生存期(PFS)和总生存期(OS),采用Kaplan-Meier方法进行单因素分析。差异的显著性采用Mantel-Cox log-rank检验。显著性参数进入多重Cox回归。结果:总共有51例患者(平均年龄56岁)进入研究。多维尔评分均为4分(14/51;28%)或5 (37/51;72%)。在一个月时,28%的患者表现出完全的代谢反应,而72%的患者有18f - fdg显著残留疾病。在治疗后1个月的扫描中,残留病变患者的SUVmax、SUVpeak、SUVmax-to- liver比值和MTV均显著降低。对于PFS的评估,血清LDH、治疗后1个月suvmax / liver比值、治疗后1个月TLG和基线Dmax进入多变量分析。治疗后1个月suvmax / liver比值(危险比[HR] = 5.21;p = 0.004)和基线Dmax (HR = 13.8;p = 0.013)保持显著性,是PFS的独立预测因子。对于OS,将血清LDH、delta SUVmean-to-liver ratio、delta百分比TLG和治疗后1个月Dmax纳入多因素分析。δ百分比TLG (HR = 4.37;p = 0.023)作为OS的独立预测因子仍然显著。结论:治疗后早期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。最重要的预后预测因子是疾病的基线程度、治疗后1个月的贪婪度以及从基线开始代谢负担的变化。
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来源期刊
Cancer Imaging
Cancer Imaging ONCOLOGY-RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING
CiteScore
7.00
自引率
0.00%
发文量
66
审稿时长
>12 weeks
期刊介绍: Cancer Imaging is an open access, peer-reviewed journal publishing original articles, reviews and editorials written by expert international radiologists working in oncology. The journal encompasses CT, MR, PET, ultrasound, radionuclide and multimodal imaging in all kinds of malignant tumours, plus new developments, techniques and innovations. Topics of interest include: Breast Imaging Chest Complications of treatment Ear, Nose & Throat Gastrointestinal Hepatobiliary & Pancreatic Imaging biomarkers Interventional Lymphoma Measurement of tumour response Molecular functional imaging Musculoskeletal Neuro oncology Nuclear Medicine Paediatric.
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