不同阈值的基线代谢和体积[18F]FDG PET参数对接受car - t细胞治疗的DLBCL患者早期治疗失败和死亡风险的预测能力

IF 1.8 Q3 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING
Emil Novruzov , Helena A. Peters , Kai Jannusch , Guido Kobbe , Sascha Dietrich , Johannes C. Fischer , Jutta Rox , Gerald Antoch , Frederik L. Giesel , Christina Antke , Ben-Niklas Baermann , Eduards Mamlins
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引用次数: 0

摘要

目的:[18F]FDG成像是car - t细胞治疗复发性或难治性DLBCL患者管理的重要组成部分。具体成像参数预测能力的计算方法仍是一个谜。在这项回顾性研究中,我们试图评估基线代谢参数和通过不同阈值方法自动分割计算的肿瘤负荷对DLBCL患者早期治疗失败和死亡风险的预测能力。材料和方法:纳入18名成年患者,他们在2018年12月至2023年10月的30天和90天内接受了car - t细胞治疗,同时进行了至少一次治疗前和两次治疗后[18F]FDG PET扫描。基于SUVmax > 4.0的固定绝对阈值、等值线> 40 %的相对绝对阈值、肝脏SUV值及其2个 SD值的背景阈值和仅肝脏SUV值的概念,我们在提取SUV参数的基础上,对voi进行了一键式自动分割,计算出mtv和tlg。结果:对于早期治疗失败,基线代谢参数如SUVmax、SUVpeak和SUVmean往往比基线代谢负担具有更大的预测能力。然而,无论采用何种阈值法,基线代谢负担在预测死亡风险方面都更优越。结论:本研究表明,使用不同阈值的代谢性肿瘤负荷自动描述方法在结果上没有实质性差异。因此,目前的临床标准将SUV > 4.0作为固定的绝对阈值似乎是一个可行的选择。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The predictive power of baseline metabolic and volumetric [18F]FDG PET parameters with different thresholds for early therapy failure and mortality risk in DLBCL patients undergoing CAR-T-cell therapy

Objective

[18F]FDG imaging is an integral part of patient management in CAR-T-cell therapy for recurrent or therapy-refractory DLBCL. The calculation methods of predictive power of specific imaging parameters still remains elusive. With this retrospective study, we sought to evaluate the predictive power of the baseline metabolic parameters and tumor burden calculated with automated segmentation via different thresholding methods for early therapy failure and mortality risk in DLBCL patients.

Materials and methods

Eighteen adult patients were enrolled, who underwent CAR-T-cell therapy accompanied by at least one pretherapeutic and two posttherapeutic [18F]FDG PET scans within 30 and 90 days between December 2018 and October 2023. We performed single-click automatic segmentation within VOIs in addition to extracting the SUV parameters to calculate the MTVs and TLGs by applying thresholds based on the concepts of a fixed absolute threshold with an SUVmax > 4.0, a relative absolute threshold with an isocontour of > 40 % of the SUVmax, a background threshold involving the addition of the liver SUV value and its 2 SD values, and only the liver SUV value.

Results

For early therapy failure, baseline metabolic parameters such as the SUVmax, SUVpeak and SUVmean tended to have greater predictive power than did the baseline metabolic burden. However, the baseline metabolic burden was superior in the prediction of mortality risk regardless of the thresholding method used.

Conclusion

This study revealed that automated delineation methods of metabolic tumor burden using different thresholds do not differ in outcome substantially. Therefore, the current clinical standard with a fixed absolute threshold value of SUV > 4.0 seems to be a feasible option.
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来源期刊
European Journal of Radiology Open
European Journal of Radiology Open Medicine-Radiology, Nuclear Medicine and Imaging
CiteScore
4.10
自引率
5.00%
发文量
55
审稿时长
51 days
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