Prognostic Value of Somatostatin Receptor-Derived Volumetric Parameters from a Hybrid Standardized Uptake Value Thresholding Method in Patients with 68Ga-DOTATATE-Avid Stage IV Neuroendocrine Neoplasms: A Preliminary Study.

IF 2.8 2区 医学 Q2 ENDOCRINOLOGY & METABOLISM
Neuroendocrinology Pub Date : 2024-01-01 Epub Date: 2023-04-21 DOI:10.1159/000530771
Zhaoting Cheng, Sijuan Zou, Jianyuan Zhou, Shuang Song, Yuankai Zhu, Jun Zhao, Xiaohua Zhu
{"title":"Prognostic Value of Somatostatin Receptor-Derived Volumetric Parameters from a Hybrid Standardized Uptake Value Thresholding Method in Patients with 68Ga-DOTATATE-Avid Stage IV Neuroendocrine Neoplasms: A Preliminary Study.","authors":"Zhaoting Cheng, Sijuan Zou, Jianyuan Zhou, Shuang Song, Yuankai Zhu, Jun Zhao, Xiaohua Zhu","doi":"10.1159/000530771","DOIUrl":null,"url":null,"abstract":"<p><strong>Introduction: </strong>The ability of PET/CT imaging to delineate neuroendocrine neoplasms (NENs) and predict prognosis in affected patients is often compromised by substantial uptake heterogeneity. We hereby proposed a hybrid standardized uptake value (SUV) thresholding algorithm to extract volumetric parameters from somatostatin receptor (SSTR) PET/CT imaging and investigate their prognostic performance in patients with 68Ga-DOTATATE-avid stage IV NENs.</p><p><strong>Methods: </strong>For 38 retrospectively enrolled patients, we used either fixed SUV thresholding of normal liver parenchyma (method A), 41% of the SUVmax for each lesion (method B), or a hybrid method (method A for liver metastases; fixed SUV threshold of normal bone for bone metastases; method B for primary tumors and other metastases) to quantify the whole-body SSTR-expressing tumor volume (SRETVwb) and total lesion SSTR expression (TLSREwb). Patient survival was also recorded and analyzed.</p><p><strong>Results: </strong>PET/CT images revealed heterogeneous uptake of 68Ga-DOTATATE at primary and metastatic sites. Progression-free survival (PFS) and overall survival (OS) were negatively correlated with the extent of liver or bone metastases (p &lt; 0.05), but not significantly correlated with tumor grade or 18F-FDG PET/CT positivity. By the hybrid method, PFS was significantly shorter in patients with high SRETVwb, and OS was significantly shorter in those with high SRETVwb and TLSREwb (p &lt; 0.05). However, when derived from method A or method B, neither SRETVwb nor TLSREwb could predict patient outcomes.</p><p><strong>Conclusion: </strong>Compared with other methods used in 68Ga-DOTATATE-avid stage IV NENs, our hybrid SUV thresholding method demonstrated robustness, with greater precision, reliability, and prognostic power.</p>","PeriodicalId":19117,"journal":{"name":"Neuroendocrinology","volume":" ","pages":"805-815"},"PeriodicalIF":2.8000,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Neuroendocrinology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1159/000530771","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2023/4/21 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"ENDOCRINOLOGY & METABOLISM","Score":null,"Total":0}
引用次数: 0

Abstract

Introduction: The ability of PET/CT imaging to delineate neuroendocrine neoplasms (NENs) and predict prognosis in affected patients is often compromised by substantial uptake heterogeneity. We hereby proposed a hybrid standardized uptake value (SUV) thresholding algorithm to extract volumetric parameters from somatostatin receptor (SSTR) PET/CT imaging and investigate their prognostic performance in patients with 68Ga-DOTATATE-avid stage IV NENs.

Methods: For 38 retrospectively enrolled patients, we used either fixed SUV thresholding of normal liver parenchyma (method A), 41% of the SUVmax for each lesion (method B), or a hybrid method (method A for liver metastases; fixed SUV threshold of normal bone for bone metastases; method B for primary tumors and other metastases) to quantify the whole-body SSTR-expressing tumor volume (SRETVwb) and total lesion SSTR expression (TLSREwb). Patient survival was also recorded and analyzed.

Results: PET/CT images revealed heterogeneous uptake of 68Ga-DOTATATE at primary and metastatic sites. Progression-free survival (PFS) and overall survival (OS) were negatively correlated with the extent of liver or bone metastases (p < 0.05), but not significantly correlated with tumor grade or 18F-FDG PET/CT positivity. By the hybrid method, PFS was significantly shorter in patients with high SRETVwb, and OS was significantly shorter in those with high SRETVwb and TLSREwb (p < 0.05). However, when derived from method A or method B, neither SRETVwb nor TLSREwb could predict patient outcomes.

Conclusion: Compared with other methods used in 68Ga-DOTATATE-avid stage IV NENs, our hybrid SUV thresholding method demonstrated robustness, with greater precision, reliability, and prognostic power.

在 68Ga-DOTATATE-Avid IV 期神经内分泌肿瘤患者中,通过混合标准化摄取值阈值法得出的体生长激素受体体积参数的预后价值:初步研究。
简介:正电子发射计算机断层显像/计算机断层扫描成像(PET/CT)划分神经内分泌肿瘤(NENs)和预测受影响患者预后的能力往往受到大量摄取异质性的影响。在此,我们提出了一种混合标准化摄取值(SUV)阈值算法,用于从体泌素受体(SSTR)PET/CT成像中提取容积参数,并研究其在68Ga-DOTATATE-avid IV期NEN患者中的预后表现:对于38例回顾性入组患者,我们使用正常肝实质的固定SUV阈值(方法A)、每个病灶SUVmax的41%(方法B)或混合方法(方法A用于肝转移;方法B用于原发肿瘤和其他转移灶)来量化全身SSTR表达肿瘤体积(SRETVwb)和总病灶SSTR表达(TLSREwb)。此外,还记录并分析了患者的生存情况:结果:PET/CT图像显示,68Ga-DOTATATE在原发和转移部位均有不同程度的摄取。无进展生存期(PFS)和总生存期(OS)与肝转移或骨转移的程度呈负相关(p < 0.05),但与肿瘤分级或 18F-FDG PET/CT 阳性无明显相关性。根据混合方法,高 SRETVwb 患者的 PFS 明显较短,高 SRETVwb 和 TLSREwb 患者的 OS 明显较短(p < 0.05)。然而,从方法 A 或方法 B 得出的 SRETVwb 和 TLSREwb 都不能预测患者的预后:与其他用于68Ga-DOTATATE-avid IV期NEN的方法相比,我们的混合SUV阈值法表现出稳健性,具有更高的精确度、可靠性和预后能力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Neuroendocrinology
Neuroendocrinology 医学-内分泌学与代谢
CiteScore
8.30
自引率
2.40%
发文量
50
审稿时长
6-12 weeks
期刊介绍: ''Neuroendocrinology'' publishes papers reporting original research in basic and clinical neuroendocrinology. The journal explores the complex interactions between neuronal networks and endocrine glands (in some instances also immunecells) in both central and peripheral nervous systems. Original contributions cover all aspects of the field, from molecular and cellular neuroendocrinology, physiology, pharmacology, and the neuroanatomy of neuroendocrine systems to neuroendocrine correlates of behaviour, clinical neuroendocrinology and neuroendocrine cancers. Readers also benefit from reviews by noted experts, which highlight especially active areas of current research, and special focus editions of topical interest.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信