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淋巴瘤患者网状内皮系统内弥漫性氟-18-氟脱氧葡萄糖(F-FDG)摄取增加的预后意义。

Prognostic significance of diffuse increased fluorine-18-fluorodeoxyglucose (F-FDG) uptake within the reticuloendothelial system in lymphoma patients.

作者信息

Zhao Zixuan, Zhou Yeye, Yao Xiaodong, Ge Shushan, Sang Shibiao, Yang Yi, Zhang Bin, Deng Shengming

机构信息

Department of Nuclear Medicine, the First Affiliated Hospital of Soochow University, Suzhou, China.

Department of Medical Cosmetology, Department of Dermatology, Affiliated Hospital of Nantong University, Nantong, China.

出版信息

Quant Imaging Med Surg. 2024 Sep 1;14(9):6374-6385. doi: 10.21037/qims-24-180. Epub 2024 Aug 28.

Abstract

BACKGROUND

As constituents of the reticuloendothelial system, the spleen and bone marrow (BM) have been recognized as integral components of the systemic inflammatory response in cancer contexts, thereby serving as predictive indicators for assessing cancer prognosis. Fluorine-18-fluorodeoxyglucose (F-FDG) positron emission tomography (PET)/computed tomography (CT) has attained widespread utilization for staging, assessing treatment response, and prognostication in lymphoma patients. Several investigations have proposed that focal increased F-FDG uptake in the BM or spleen may correlate with malignant involvement in lymphoma. However, scant data exist regarding the implications of diffuse BM and splenic uptake. This study aimed to explore the relationships between metabolic parameters of the spleen and BM on F-FDG PET/CT and inflammatory markers, and to assess their prognostic value in patients with lymphoma.

METHODS

A retrospective analysis was conducted on 118 patients newly diagnosed with malignant lymphoma, who underwent F-FDG PET/CT and exhibited diffuse increased splenic or BM uptake in F-FDG PET/CT imaging. The mean standardized uptake value (SUV) of the spleen, BM, and liver was calculated. The association between metabolic variables and systemic inflammatory markers was investigated, and the prognostic significance of clinicopathological and PET parameters was assessed using overall survival (OS) and progression-free survival (PFS).

RESULTS

A statistically significant correlation was found between the spleen-to-liver SUV ratio (SLR) and inflammatory markers such as C-reactive protein (r=0.264, P=0.007) and platelet-to-lymphocyte ratio (r=0.227, P=0.021). No significant correlation was observed between BM-to-liver SUV ratio (BLR) and hematologic parameters, while concordance analysis revealed a fair agreement between BLR and bone marrow biopsy (BMB) (Cohen's Kappa-κ =0.271, P=0.002). In patients with aggressive non-Hodgkin lymphoma, both SLR [P=0.017, HR 2.715, 95% confidence interval (CI): 0.875-8.428] and BLR (P=0.044, HR 0.795, 95% CI: 0.348-1.813) were significantly linked to OS, while SLR (P=0.019, HR 2.223, 95% CI: 1.139-4.342) emerged as a significant prognostic factor for PFS.

CONCLUSIONS

This study highlighted that diffuse increased splenic F-FDG uptake in lymphoma patients was closely associated with inflammation, whereas diffuse BM uptake was likely attributable to BM infiltration rather than inflammatory changes. Furthermore, both parameters held promise as prognostic indicators for patients with aggressive lymphoma.

摘要

背景

作为网状内皮系统的组成部分,脾脏和骨髓已被视为癌症背景下全身炎症反应的重要组成部分,从而作为评估癌症预后的预测指标。氟-18-氟脱氧葡萄糖(F-FDG)正电子发射断层扫描(PET)/计算机断层扫描(CT)已广泛应用于淋巴瘤患者的分期、评估治疗反应和预后。多项研究表明,骨髓或脾脏中局灶性F-FDG摄取增加可能与淋巴瘤的恶性浸润有关。然而,关于弥漫性骨髓和脾脏摄取的意义的数据却很少。本研究旨在探讨F-FDG PET/CT上脾脏和骨髓的代谢参数与炎症标志物之间的关系,并评估它们在淋巴瘤患者中的预后价值。

方法

对118例新诊断为恶性淋巴瘤且在F-FDG PET/CT成像中表现为脾脏或骨髓弥漫性摄取增加的患者进行回顾性分析。计算脾脏、骨髓和肝脏的平均标准化摄取值(SUV)。研究代谢变量与全身炎症标志物之间 的关联,并使用总生存期(OS)和无进展生存期(PFS)评估临床病理和PET参数的预后意义。

结果

脾脏与肝脏的SUV比值(SLR)与C反应蛋白等炎症标志物(r=0.264,P=0.007)和血小板与淋巴细胞比值(r=0.227,P=0.021)之间存在统计学上的显著相关性。骨髓与肝脏的SUV比值(BLR)与血液学参数之间未观察到显著相关性,而一致性分析显示BLR与骨髓活检(BMB)之间有较好的一致性(科恩卡方系数κ=0.271,P=0.002)。在侵袭性非霍奇金淋巴瘤患者中,SLR(P=0.017,HR 2.715,95%置信区间[CI]:0.875-8.428)和BLR(P=0.044,HR 0.795,95%CI:0.348-1.813)均与OS显著相关,而SLR(P=0.019,HR 2.223,95%CI:1.139-4.342)是PFS的显著预后因素。

结论

本研究强调,淋巴瘤患者脾脏F-FDG摄取弥漫性增加与炎症密切相关,而骨髓弥漫性摄取可能归因于骨髓浸润而非炎症变化。此外,这两个参数都有望成为侵袭性淋巴瘤患者的预后指标。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea9d/11400674/f0d310aafb15/qims-14-09-6374-f1.jpg

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