PSMA PET/CT基线参数预测转移性去势抵抗性前列腺癌患者的总生存期和治疗反应。

IF 4.7 2区 医学 Q1 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING
European Radiology Pub Date : 2025-07-01 Epub Date: 2025-01-22 DOI:10.1007/s00330-025-11360-3
Fleur Kleiburg, Lioe-Fee de Geus-Oei, Romy Spijkerman, Wyanne A Noortman, Floris H P van Velden, Srirang Manohar, Frits Smit, Frank A J Toonen, Saskia A C Luelmo, Tom van der Hulle, Linda Heijmen
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引用次数: 0

摘要

目的:转移性去势抵抗性前列腺癌(mCRPC)是一种异质性疾病,具有不同的生存结局。本研究调查了PSMA PET/CT基线参数是否与生存和治疗反应相关。方法:60例mCRPC患者在接受雄激素受体靶向药物(ARTAs)或化疗前行PSMA-1007 PET/CT检查[18F]。收集基于强度的参数、体积参数、转移部位和基线PSMA PET/CT的DmaxVox(两个最外层体素之间的距离),以及年龄、Gleason评分和实验室参数。Cox回归分析评估其对总生存期(OS)的预后价值。此外,我们进行了初步的病变水平分析(n = 241个病变),包括病变位置和从先前文献中选择的12个放射学特征。Logistic回归评估了它们与治疗3-4个月后PSMA PET/ ct病变进展的关系。结果:肿瘤总体积(PSMA-TV) (HR = 1.41 /倍[1.17-1.70])、病变总摄取(TL-PSMA) (HR = 1.40 /倍[1.16-1.69])和DmaxVox (HR = 1.31 / 10 cm增加[1.07-1.62])是OS的预后指标,与基线PSA水平(HR = 0.82 /倍[0.68-0.98])、血红蛋白水平(HR = 0.68 / mmol/L增加[0.49-0.95])和治疗线无关。在病变水平上,位置(前列腺vs骨OR = 0.23[0.06-0.83])和SUVmean (OR = 1.72 /倍[1.08-2.75])是病变进展的独立预后标志物,形态学和基于纹理的放射学特征不是。结论:PSMA PET/CT基线扫描对mCRPC患者具有预后价值,可能有助于治疗决策。当没有自动分割软件时,DmaxVox可以作为PSMA-TV的更简单的替代方案。当与PSMA-TV联合使用时,较低的PSA水平表明较差的OS,这可能是肿瘤去分化的标志。需要进一步的研究来验证这些模型在更大的患者群体中的有效性。mccrpc是一种高度异质性的疾病,需要良好的预后指标。发现PSMA-TV是OS的最佳独立预后指标;病变间最大距离(DmaxVox)可以作为一种更简单的替代方法。代表肿瘤负担的PSMA PET/CT基线参数与mCRPC患者的OS独立相关,为临床决策提供预后见解。虽然PSMA-TV是最好的预后指标,但DmaxVox可以作为更容易获得的替代指标。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Baseline PSMA PET/CT parameters predict overall survival and treatment response in metastatic castration-resistant prostate cancer patients.

Objective: Metastatic castration-resistant prostate cancer (mCRPC) is a heterogeneous disease with varying survival outcomes. This study investigated whether baseline PSMA PET/CT parameters are associated with survival and treatment response.

Methods: Sixty mCRPC patients underwent [18F]PSMA-1007 PET/CT before treatment with androgen receptor-targeted agents (ARTAs) or chemotherapy. Intensity-based parameters, volumetric parameters, metastatic sites and DmaxVox (distance between the two outermost voxels) from baseline PSMA PET/CT were collected, as well as age, Gleason score and laboratory parameters. Cox regression analysis evaluated their prognostic value for overall survival (OS). Additionally, a preliminary lesion-level analysis was done (n = 241 lesions) with lesion location and twelve radiomic features selected from previous literature. Logistic regression evaluated their association with PSMA PET/CT-based lesion progression after 3-4 months of treatment.

Results: Total tumour volume (PSMA-TV) (HR = 1.41 per doubling [1.17-1.70]), total lesion uptake (TL-PSMA) (HR = 1.40 per doubling [1.16-1.69]) and DmaxVox (HR = 1.31 per 10 cm increase [1.07-1.62]) were prognostic for OS, each independent of baseline PSA level (HR = 0.82 per doubling [0.68-0.98]), haemoglobin level (HR = 0.68 per mmol/L increase [0.49-0.95]) and line of treatment. On lesion-level, location (prostate vs bone OR = 0.23 [0.06-0.83]) and SUVmean (OR = 1.72 per doubling [1.08-2.75]) were independent prognostic markers for lesion progression, morphological and texture-based radiomic features were not.

Conclusion: Baseline PSMA PET/CT scans have prognostic value in mCRPC patients and can potentially aid in treatment decision-making. DmaxVox can serve as a simpler alternative to PSMA-TV when automated segmentation software is not available. When combined with PSMA-TV, lower PSA levels indicated worse OS, which may be a marker of tumour dedifferentiation. Further research is needed to validate these models in larger patient cohorts.

Key points: Question mCRPC is a highly heterogeneous disease, requiring good prognostic markers. Findings PSMA-TV was the best independent prognostic marker for OS; maximum distance between lesions (DmaxVox) can be used as a simpler alternative. Clinical relevance Baseline PSMA PET/CT parameters representing tumour burden were independently associated with OS in mCRPC patients, providing prognostic insights for clinical decision-making. Although PSMA-TV was the best prognostic marker, DmaxVox can serve as an easier to obtain alternative.

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来源期刊
European Radiology
European Radiology 医学-核医学
CiteScore
11.60
自引率
8.50%
发文量
874
审稿时长
2-4 weeks
期刊介绍: European Radiology (ER) continuously updates scientific knowledge in radiology by publication of strong original articles and state-of-the-art reviews written by leading radiologists. A well balanced combination of review articles, original papers, short communications from European radiological congresses and information on society matters makes ER an indispensable source for current information in this field. This is the Journal of the European Society of Radiology, and the official journal of a number of societies. From 2004-2008 supplements to European Radiology were published under its companion, European Radiology Supplements, ISSN 1613-3749.
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