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R/R DLBCL 中 CAR-T 细胞治疗期间的标准化 FDG-PET 判读:一项 DESCAR-T 研究

英文原题:Standardized FDG-PET interpretation during CAR T-cell therapy in R/R DLBCL: a DESCAR-T study.

查看英文原题

Standardized FDG-PET interpretation during CAR T-cell therapy in R/R DLBCL: a DESCAR-T study.

PubMed 2026/07/25(内容时间) Eur J Nucl Med Mol Imaging Q1 · IF 7.6(JCR 2025)

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研究概要

基线的 TMTV 和通过 DS 评估的代谢反应,以及随访 PET/CT 上的残留 TMTV,是接受 anti-CD19 CAR T-cells 治疗的 R/R DLBCL 患者强有力的预后生物标志物。

研究思路结论见上方概要

CAR-T 细胞疗法已改变复发/难治性(R/R)弥漫性大B细胞淋巴瘤(DLBCL)的管理。氟脱氧葡萄糖正电子发射断层扫描/计算机断层扫描(PET/CT)在淋巴瘤疗效评估中发挥核心作用,但其在这一背景下的预后应用仍缺乏充分标准化。

来自法国DESCAR-T 登记处的患者,在真实世界中接受商业化抗CD19 CAR-T 细胞作为三线或更后线治疗,并且在输注前以及输注后1个月(M1)或3个月(M3)有经中心审阅的PET/CT,被纳入研究。每次访视时,测量总代谢肿瘤体积(TMTV)和SUVmax。在随访PET/CT上记录Deauville评分(DS)以及根据2014 Lugano分类的疗效反应。确定基线、M1和M3随访时用于无进展生存期(PFS)和总生存期(OS)的最佳TMTV截断值,以及M1和M3时DS的预后影响。

共分析了212例R/R DLBCL患者。基线中位SUVmax为16.4,中位TMTV为41.3 cm3。基线TMTV截断值为30 cm 3,与LDH一起,在单变量和多变量分析中均显著区分患者的PFS和OS。M1时完全代谢缓解(DS 1-3)与较DS4-5更好的PFS M1和OS M1显著相关(对于PFS M1:中位为21.8 vs 1.8 vs 个月;p < 0.0001;对于OS M1:中位未达到 vs 中位为6.3个月;p < 0.0001)。DS5识别出结局最差的患者(对于PFS M1:中位为0.1个月;对于OS M1:中位为4.5个月)。同样,在M3时,DS1-3与较DS4-5更好的结局相关,且DS5患者结局最差。在未达到完全代谢缓解的患者中,残留TMTV提供了额外的预后价值。

展开英文摘要原文

CAR T-cell therapy has changed the management of relapsed/refractory (R/R) Diffuse large B-cell lymphoma (DLBCL). Fluorodeoxyglucose Positron Emission Tomography Computed Tomography (PET/CT) plays a central role in lymphoma response assessment, but its prognostic use remains insufficiently standardized in this setting.

Patients from the French DESCAR-T registry treated in third line or beyond with commercial anti-CD19 CAR T-cells in real-life, and having centrally reviewed PET/CT before infusion, and at one month (M1) or three months (M3) post-infusion were included. For each visit, Total Metabolic Tumor Volume (TMTV) and SUVmax were measured. Deauville score (DS) and response according to 2014 Lugano classification were registered on follow-up PET/CT. Optimal TMTV cut-offs at baseline, M1 and M3 follow-up for progression-free survival (PFS) and overall survival (OS) and the prognostic impact of DS at M1 and M3 were determined.

A total of 212 R/R DLBCL patients were analysed. Baseline median SUVmax was 16.4 and median TMTV 41.3 cm3. A baseline TMTV cut-off of 30 cm 3 significantly stratified patients for PFS and OS, in both univariate and multivariate analysis, along with LDH. Complete metabolic response (DS 1-3) at M1 was significantly associated with better PFS M1 and OS M1 than DS4-5 (for PFS M1 : median of 21.8 vs 1.8 vs months; p < 0.0001; for OS M1 : median not reached versus median of 6.3 months; p < 0.0001). DS5 identified patients with the worst outcomes (for PFS M1 : median of 0.1 month and for OS M1 : median of 4.5 months). Similarly, at M3 DS1-3 was associated with a better outcome than DS4-5, and patients with DS5 had the worst outcome. In patients without complete metabolic response residual TMTV provided additional prognostic value.

Baseline TMTV and metabolic response assessed by DS, together with residual TMTV on follow-up PET/CT, are strong prognostic biomarkers in R/R DLBCL patients treated with anti-CD19 CAR T-cells.

论文信息

作者
Al Tabaa Y、Bailly C、Palard-Novello X、Cottereau AS、Tordo J、Sesques P、Cartron G、Houot R
第一作者单位
Scintidoc Nuclear Medicine Center, 25 Rue de Cl&#xe9;mentville, 34070, Montpellier, France.France
通讯作者单位
Department of Nuclear Medicine, Saint-Louis Hospital, AP-HP, INSERM UMR_S942, Universit&#xe9; Paris Cit&#xe9;, Paris, France. laetitia.vercellino@aphp.fr.France
期刊
European journal of nuclear medicine and molecular imaging2026 Jul 25
原文标识
PubMed 42501071 · DOI 10.1007/s00259-026-08055-2