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基线及早期反应 FDG-PET/CT 在接受 CAR-T 细胞治疗的复发/难治性侵袭性 B 细胞淋巴瘤患者中的预后价值

英文原题:Prognostic value of baseline and early response FDG-PET/CT in patients with refractory and relapsed aggressive B-cell lymphoma undergoing CAR-T cell therapy.

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Prognostic value of baseline and early response FDG-PET/CT in patients with refractory and relapsed aggressive B-cell lymphoma undergoing CAR-T cell therapy.

PubMed 2023/01/20(内容时间) J Cancer Res Clin Oncol Q2 · IF 3.3(JCR 2025)

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研究概要

我们的结果证实了 PET-1 的预后价值。42% 的所有 CMR 患者在 CAR-T 细胞治疗后 1 年仍处于缓解状态。90% 的非 CMR 患者复发,表明需要早期干预。CAR-T 细胞输注前较高的 TMTV 与较低的 CMR 机会相关。

研究思路结论见上方概要

嵌合抗原受体(CAR)-T细胞是复发/难治性(r/r)侵袭性B细胞淋巴瘤患者的一种可行治疗选择。CAR-T 细胞治疗后复发患者的预后不佳,需要确定预测结局的因素。我们的目的是评估FDG-PET/CT在预测患者结局方面的价值。

22例接受tisagenlecleucel(n = 17)或axicabtagene ciloleucel(n = 5)CAR-T 细胞治疗的r/r B细胞淋巴瘤患者,在CAR-T 细胞输注前(PET-0)和输注后1个月(PET-1)接受了定量FDG-PET/CT检查。PET-1被分类为完全代谢缓解(CMR,Deauville评分1-3)或非CMR(Deauville评分4-5)。

在PET-1时,12/22(55%)患者显示CMR,十名(45%)患者为非CMR。7/12(58%)CMR患者在中位223天后复发,其中三名(25%)死亡。9/10(90%)非CMR患者在中位91天后出现复发或疾病进展,其中八名(80%)死亡。CMR患者在PET-0中显示的中位总代谢肿瘤体积(TMTV)显著低于非CMR患者(1 ml vs 225 ml)。

展开英文摘要原文

Chimeric antigen receptor (CAR)-T cells are a viable treatment option for patients with relapsed or refractory (r/r) aggressive B-cell lymphomas. The prognosis of patients who relapse after CAR-T cell treatment is dismal and factors predicting outcomes need to be identified. Our aim was to assess the value of FDG-PET/CT in terms of predicting patient outcomes.

Twenty-two patients with r/r B-cell lymphoma who received CAR-T cell treatment with tisagenlecleucel (n = 17) or axicabtagene ciloleucel (n = 5) underwent quantitative FDG-PET/CT before (PET-0) and 1 month after infusion of CAR-T cells (PET-1). PET-1 was classified as complete metabolic response (CMR, Deauville score 1-3) or non-CMR (Deauville score 4-5).

At the time of PET-1, 12/22 (55%) patients showed CMR, ten (45%) patients non-CMR. 7/12 (58%) CMR patients relapsed after a median of 223 days, three of them (25%) died. 9/10 (90%) non-CMR patients developed relapse or progressive disease after a median of 91 days, eight of them (80%) died. CMR patients demonstrated a significantly lower median total metabolic tumor volume (TMTV) in PET-0 (1 ml) than non-CMR patients (225 ml).

Our results confirm the prognostic value of PET-1. 42% of all CMR patients are still in remission 1 year after CAR T-cell treatment. 90% of the non-CMR patients relapsed, indicating the need for early intervention. Higher TMTV before CAR-T cell infusion was associated with lower chances of CMR.

论文信息

作者
Georgi TW、Kurch L、Franke GN、Jentzsch M、Schwind S、Perez-Fernandez C、Petermann N、Merz M
第一作者单位
Department of Nuclear Medicine, University of Leipzig, Leipzig, Germany.Germany
通讯作者单位
Medical Clinic I, Department of Hematology, Cellular Therapy and Hemostaseology, University of Leipzig, Liebigstr. 22, 04103, Leipzig, Germany. vladan.vucinic@medizin.uni-leipzig.de.Germany
期刊
Journal of cancer research and clinical oncology2023 Aug
原文标识
PubMed 36662305 · DOI 10.1007/s00432-023-04587-4