Positron Emission Tomography Molecular Imaging for Phenotyping and Management of Lymphoma.

IF 3.7 Q2 GENETICS & HEREDITY
Xiaohui Zhang, Han Jiang, Shuang Wu, Jing Wang, Rui Zhou, Xuexin He, Shufang Qian, Shuilin Zhao, Hong Zhang, Ali Cahid Civelek, Mei Tian
{"title":"Positron Emission Tomography Molecular Imaging for Phenotyping and Management of Lymphoma.","authors":"Xiaohui Zhang,&nbsp;Han Jiang,&nbsp;Shuang Wu,&nbsp;Jing Wang,&nbsp;Rui Zhou,&nbsp;Xuexin He,&nbsp;Shufang Qian,&nbsp;Shuilin Zhao,&nbsp;Hong Zhang,&nbsp;Ali Cahid Civelek,&nbsp;Mei Tian","doi":"10.1007/s43657-021-00042-x","DOIUrl":null,"url":null,"abstract":"<p><p>Positron emission tomography (PET) represents molecular imaging for non-invasive phenotyping of physiological and biochemical processes in various oncological diseases. PET imaging with <sup>18</sup>F-fluorodeoxyglucose (<sup>18</sup>F-FDG) for glucose metabolism evaluation is the standard imaging modality for the clinical management of lymphoma. One of the <sup>18</sup>F-FDG PET applications is the detection and pre-treatment staging of lymphoma, which is highly sensitive. <sup>18</sup>F-FDG PET is also applied during treatment to evaluate the individual chemo-sensitivity and accordingly guide the response-adapted therapy. At the end of the therapy regiment, a negative PET scan is indicative of a good prognosis in patients with advanced Hodgkin's lymphoma and diffuse large B-cell lymphoma. Thus, adjuvant radiotherapy may be alleviated. Future PET studies using non-<sup>18</sup>F-FDG radiotracers, such as <sup>68</sup>Ga-labeled pentixafor (a cyclic pentapeptide that enables sensitive and high-contrast imaging of C-X-C motif chemokine receptor 4), <sup>68</sup>Ga-labeled fibroblast activation protein inhibitor (FAPI) that reflects the tumor microenvironment, and <sup>89</sup>Zr-labeled atezolizumab that targets the programmed cell death-ligand 1 (PD-L1), may complement <sup>18</sup>F-FDG and offer essential tools to decode lymphoma phenotypes further and identify the mechanisms of lymphoma therapy.</p>","PeriodicalId":74435,"journal":{"name":"Phenomics (Cham, Switzerland)","volume":"2 2","pages":"102-118"},"PeriodicalIF":3.7000,"publicationDate":"2022-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9590515/pdf/43657_2021_Article_42.pdf","citationCount":"6","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Phenomics (Cham, Switzerland)","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1007/s43657-021-00042-x","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"GENETICS & HEREDITY","Score":null,"Total":0}
引用次数: 6

Abstract

Positron emission tomography (PET) represents molecular imaging for non-invasive phenotyping of physiological and biochemical processes in various oncological diseases. PET imaging with 18F-fluorodeoxyglucose (18F-FDG) for glucose metabolism evaluation is the standard imaging modality for the clinical management of lymphoma. One of the 18F-FDG PET applications is the detection and pre-treatment staging of lymphoma, which is highly sensitive. 18F-FDG PET is also applied during treatment to evaluate the individual chemo-sensitivity and accordingly guide the response-adapted therapy. At the end of the therapy regiment, a negative PET scan is indicative of a good prognosis in patients with advanced Hodgkin's lymphoma and diffuse large B-cell lymphoma. Thus, adjuvant radiotherapy may be alleviated. Future PET studies using non-18F-FDG radiotracers, such as 68Ga-labeled pentixafor (a cyclic pentapeptide that enables sensitive and high-contrast imaging of C-X-C motif chemokine receptor 4), 68Ga-labeled fibroblast activation protein inhibitor (FAPI) that reflects the tumor microenvironment, and 89Zr-labeled atezolizumab that targets the programmed cell death-ligand 1 (PD-L1), may complement 18F-FDG and offer essential tools to decode lymphoma phenotypes further and identify the mechanisms of lymphoma therapy.

Abstract Image

Abstract Image

正电子发射断层扫描分子成像在淋巴瘤表型和治疗中的应用。
正电子发射断层扫描(PET)代表了各种肿瘤疾病生理生化过程的非侵入性分子成像。用18f -氟脱氧葡萄糖(18F-FDG)进行糖代谢评价的PET成像是淋巴瘤临床治疗的标准成像方式。18F-FDG PET的应用之一是淋巴瘤的检测和治疗前分期,这是高度敏感的。在治疗期间也应用18F-FDG PET来评估个体化疗敏感性,并相应地指导反应适应治疗。在治疗团结束时,PET扫描阴性表明晚期霍奇金淋巴瘤和弥漫性大b细胞淋巴瘤患者预后良好。因此,可以减轻辅助放疗。未来的PET研究使用非18f - fdg放射性示踪剂,如68ga标记的pentxafor(一种能够对C-X-C基序趋化因子受体4进行敏感和高对比度成像的环状五肽),68ga标记的反映肿瘤微环境的成纤维细胞激活蛋白抑制剂(FAPI),以及89zr标记的靶向程序性细胞死亡配体1 (PD-L1)的atezolizumab。可以补充18F-FDG,并为进一步解码淋巴瘤表型和确定淋巴瘤治疗机制提供必要的工具。
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
自引率
0.00%
发文量
0
×
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:481959085
Book学术官方微信