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。

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
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引用次数: 6

摘要

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。

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

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

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

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.

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