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, Han Jiang, Shuang Wu, Jing Wang, Rui Zhou, Xuexin He, Shufang Qian, Shuilin Zhao, Hong Zhang, Ali Cahid Civelek, 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.