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FDG-PET/CT 是预测和评估非霍奇金淋巴瘤(NHL)嵌合抗原受体(CAR)T 细胞治疗疗效的有力工具

英文原题:FDG-PET/CT is a powerful tool to predict and evaluate response to chimeric antigen receptor (CAR) T-cell therapy in Non-Hodgkin-Lymphoma (NHL).

查看英文原题

FDG-PET/CT is a powerful tool to predict and evaluate response to chimeric antigen receptor (CAR) T-cell therapy in Non-Hodgkin-Lymphoma (NHL).

PubMed 2024/04/09(内容时间) Nuklearmedizin Q3 · IF 1.5(JCR 2025)

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中文摘要

嵌合抗原受体(CAR)T细胞治疗显著改变了非霍奇金淋巴瘤(NHL)的治疗格局。本研究评估氟脱氧葡萄糖(FDG)正电子发射断层显像/计算机断层扫描(PET/CT)在CAR-T 治疗NHL中的疗效评估和预后判断价值。研究纳入2019年8月至2022年7月接受CAR-T 治疗的34例NHL患者。所有患者均在治疗前6天接受FDG-PET/CT(PET-0),并在CAR-T 治疗后34天接受复查(PET-1)。采用Deauville评分(DS)评估疗效,并与至少5个月的随访结果比较。19/34例(55.9%)患者PET-1的DS为3,另15例(44.1%)DS>3。PET-1时DS为3的患者中,14/19例无复发/难治性(r/r)疾病,且在末次随访时仍存活;其余5例为r/r疾病,其中4例死亡。DS>3患者中,除2例无r/r疾病外,其余13/15例均为r/r疾病,其中12例随后死亡。与PET-1时DS>3患者相比,DS=3患者无进展生存期(PFS;HR=5.7;p<0.01)和总生存期(OS;HR=5.0;p<0.01)显著更好。

此外,PET-0时DS=4的患者PFS较长呈趋势(HR=3.6;p=0.05)。CAR-T 治疗后早期采用既定DS标准开展FDG-PET/CT,是有力的治疗应答评估工具。

展开英文摘要原文

Chimeric antigen receptor (CAR) T-cell therapy has dramatically shifted the landscape of treatment especially for Non-Hodgkin-Lymphoma (NHL).

This study evaluates the role of fluorodeoxyglucose (FDG)-positron emission tomography/computed tomography (PET/CT) in NHL treated with CAR T-cell therapy concerning response assessment and prognosis.

We evaluated 34 patients with NHL who received a CAR T-cell therapy between August 2019 and July 2022. All patients underwent a pre-therapeutic FDG-PET/CT (PET-0) 6 days prior and a post-therapeutic FDG-PET/CT (PET-1) 34 days after CAR T-cell therapy. Deauville score (DS) was used for evaluation of response to therapy and compared to a minimum follow-up of 5 months. 19/34 (55. 9%) patients achieved DS 3 on PET-1, the remaining 15 (44. 1%) patients had DS > 3 on PET-1.

14/19 patients with DS 3 on PET-1 had no relapsed or refractory (r/r)-disease and were still alive at last follow-up. The other 5 patients had r/r-disease and 4 of these died. Except for two patients who had no r/r-disease, all other patients (13/15) with DS > 3 on PET-1 had r/r-disease and 12 of these subsequently died. Patients with DS 3 on PET-1 had significantly better progression free survival (PFS; HR: 5. 7; p < 0. 01) and overall survival (OS; HR: 5. 0; p < 0. 01) compared to patients with DS > 3 on PET-1.

In addition, we demonstrated that patients with DS 4 on PET-0 tended to have longer PFS (HR: 3. 6; p = 0. 05). Early FDG-PET/CT using the established DS after CAR T-cell therapy is a powerful tool to evaluate response to therapy.

论文信息

作者
Wielenberg CF、Fostitsch JC、Volz C、Marks R、Michalski K、Wäsch R、Zeiser R、Ruf J
单位
Department of Nuclear Medicine, University of Freiburg, Freiburg im Breisgau, Germany.Germany
期刊
Nuklearmedizin. Nuclear medicine2024 Aug
原文标识
PubMed 38593856 · DOI 10.1055/a-2283-8417