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细胞疗法反应的有力工具。

C. Wielenberg, J. Fostitsch, Christian Volz, Reinhard Marks, K. Michalski, Ralph Wäsch, R. Zeiser, Juri Ruf, P. T. Meyer, Claudius Klein
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摘要

嵌合抗原受体(CAR)T细胞疗法极大地改变了非霍奇金淋巴瘤(NHL)的治疗格局。本研究评估了氟脱氧葡萄糖(FDG)-正电子发射断层扫描/计算机断层扫描(PET/CT)在接受CAR T细胞疗法治疗的NHL患者中在反应评估和预后方面的作用。所有患者在接受CAR T细胞治疗前6天和治疗后34天分别接受了治疗前FDG-PET/CT(PET-0)和治疗后FDG-PET/CT(PET-1)检查。19/34(55.9%)名患者的 PET-1 DS≤ 3,其余 15(44.1%)名患者的 PET-1 DS> 3。14/19 PET-1 DS≤3 的患者没有复发或难治性(r/r)疾病,在最后一次随访时仍然存活。其他 5 名患者患有复发或难治性(r/r)疾病,其中 4 人死亡。除了两名患者没有复发或难治性疾病外,其他所有 PET-1 DS > 3 的患者(13/15)均患有复发或难治性疾病,其中 12 人随后死亡。与 PET-1 DS > 3 的患者相比,PET-1 DS ≤ 3 的患者的无进展生存期(PFS;HR:5.7;p < 0.01)和总生存期(OS;HR:5.0;p < 0.01)明显更好。此外,我们还发现,PET-0上DS≤4的患者往往有更长的PFS(HR:3.6;p = 0.05)。
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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).
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.
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