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影像生物标志物预测 CAR-T 治疗后经 ¹⁸F-FDG PET/CT 显像第 28 天达部分缓解的大 B 细胞淋巴瘤患者的结局

英文原题:Imaging Biomarkers to Predict Outcomes in Patients With Large B-Cell Lymphoma With a Day 28 Partial Response by (18)F-FDG PET/CT Imaging Following CAR-T Therapy.

查看英文原题

Imaging Biomarkers to Predict Outcomes in Patients With Large B-Cell Lymphoma With a Day 28 Partial Response by (18)F-FDG PET/CT Imaging Following CAR-T Therapy.

PubMed 2023/06/19(内容时间) Clin Lymphoma Myeloma Leuk Q1 · IF 4.1(JCR 2025)

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研究概要

我们证明,第 28 天 SUVmax 较高者在 B-OR 为 PR 的患者中显著更高,在我们的模型中,第 28 天 SUVmax 较低可能预测有利的 PFS 和 OS。此外,基线时和第 28 天时较低的 TMV 也可能预测更长的 PFS 和 OS,而基线时较低的 TLG,而非第 28 天时,与 B-OR 为 CR 显著相关。虽然需要进一步研究,但这些影像生物标志物可能有助于早期识别第 28 天 PR 且复发风险最高的患者,从而进行早期干预以改善长期结局。

研究思路结论见上方概要

在单中心接受CAR-T 治疗的75例患者中,我们回顾性识别并审查了25例(33%)在第28天达到PR的患者。PR依据2014年Lugano分类系统定义。所有患者均接受了标准治疗的CD19靶向CAR-T 疗法,使用axicabtagene ciloleucel。两名独立核医学医师使用ROVER软件测量了每处病灶(淋巴结、器官或骨髓摄取,如有)的基线(CAR-T 治疗前)和第28天PET/CT SUVmax、SUVmean和TMV(cm3)。所有统计检验均为双侧检验,显著性水平为0.05。使用R版本1.3.1099(R-studio)进行统计建模。

展开英文摘要原文

Out of 75 patients receiving CAR-T therapy at a single institution, we retrospectively identified and reviewed 25 (33%) as achieving a PR on day 28. PR was defined using the 2014 Lugano classification system. All patients received standard of care CD19 directed CAR-T therapy with axicabtagene ciloleucel. Two independent nuclear medicine physicians measured baseline (pre-CAR-T therapy) and day 28 PET/CT SUVmax, SUVmean and TMV (cm3) of each lesion (node, organ or marrow uptake, if any) using ROVER software. All statistical tests were two-sided and conducted at the 0.05 level of significance. R version 1.3.1099 (R-studio) was used for statistical modeling.

We demonstrate that a higher day 28 SUVmax was significantly higher in those with a B-OR of PR and in our modeling, a lower day 28 SUVmax may predict favorable PFS and OS. Additionally, lower TMV, both at baseline and day 28, may also be predictive of longer PFS and OS, while lower TLG at baseline, but not day 28 is significantly associated with a B-OR of CR. While further study is warranted, these imaging biomarkers may allow for early identification of those with a day 28 PR at highest risk for relapse leading to early intervention to improve long term outcomes.

论文信息

作者
Lutfi F、Goloubeva O、Kowatli A、Gryaznov A、Kim DW、Dureja R、Margiotta P、Matsumoto LR
单位
University of Maryland Marlene and Stewart Greenebaum Comprehensive Cancer Center, Baltimore, MD, United States; Division of Hematologic Malignancies and Cellular Therapeutics, University of Kansas Medical Center, Kansas City, KS, United States. Electronic address: flutfi@kumc.edu.United States
期刊
Clinical lymphoma, myeloma & leukemia2023 Oct
原文标识
PubMed 37453865 · DOI 10.1016/j.clml.2023.06.005