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肿瘤学中 CXCR4 靶向治疗学。

CXCR4-targeted theranostics in oncology.

机构信息

Department of Nuclear Medicine, University Hospital Würzburg, Oberdürrbacher Str. 6, 97080, Wurzburg, Germany.

Division of Endocrinology and Diabetes, Department of Medicine I, University Hospital, University of Würzburg, Wurzburg, Germany.

出版信息

Eur J Nucl Med Mol Imaging. 2022 Oct;49(12):4133-4144. doi: 10.1007/s00259-022-05849-y. Epub 2022 Jun 8.

DOI:10.1007/s00259-022-05849-y
PMID:35674738
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9525349/
Abstract

A growing body of literature reports on the upregulation of C-X-C motif chemokine receptor 4 (CXCR4) in a variety of cancer entities, rendering this receptor as suitable target for molecular imaging and endoradiotherapy in a theranostic setting. For instance, the CXCR4-targeting positron emission tomography (PET) agent [ Ga]PentixaFor has been proven useful for a comprehensive assessment of the current status quo of solid tumors, including adrenocortical carcinoma or small-cell lung cancer. In addition, [ Ga]PentixaFor has also provided an excellent readout for hematological malignancies, such as multiple myeloma, marginal zone lymphoma, or mantle cell lymphoma. PET-based quantification of the CXCR4 capacities in vivo allows for selecting candidates that would be suitable for treatment using the theranostic equivalent [Lu]/[Y]PentixaTher. This CXCR4-directed theranostic concept has been used as a conditioning regimen prior to hematopoietic stem cell transplantation and to achieve sufficient anti-lymphoma/-tumor activity in particular for malignant tissues that are highly sensitive to radiation, such as the hematological system. Increasing the safety margin, pretherapeutic dosimetry is routinely performed to determine the optimal activity to enhance therapeutic efficacy and to reduce off-target adverse events. The present review will provide an overview of current applications for CXCR4-directed molecular imaging and will introduce the CXCR4-targeted theranostic concept for advanced hematological malignancies.

摘要

越来越多的文献报道了 C-X-C 基序趋化因子受体 4(CXCR4)在多种癌症实体中的上调,使该受体成为治疗诊断学中分子成像和内放射治疗的合适靶点。例如,CXCR4 靶向正电子发射断层扫描(PET)剂[Ga]PentixaFor 已被证明可用于全面评估包括肾上腺皮质癌或小细胞肺癌在内的实体瘤的现状。此外,[Ga]PentixaFor 还为血液恶性肿瘤提供了出色的读数,如多发性骨髓瘤、边缘区淋巴瘤或套细胞淋巴瘤。基于 PET 的体内 CXCR4 容量定量可用于选择适合使用治疗性等效物[Lu]/[Y]PentixaTher 治疗的候选者。这种 CXCR4 导向的治疗学概念已被用作造血干细胞移植前的预处理方案,以在某些对辐射高度敏感的恶性组织中获得足够的抗淋巴瘤/肿瘤活性,如血液系统。为了提高安全性,常规进行治疗前剂量学以确定最佳活性以增强治疗效果并减少脱靶不良事件。本综述将概述 CXCR4 导向的分子成像的当前应用,并将介绍用于先进血液恶性肿瘤的 CXCR4 靶向治疗学概念。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0de1/9525349/dfc1efd2a42d/259_2022_5849_Fig7_HTML.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0de1/9525349/dfc1efd2a42d/259_2022_5849_Fig7_HTML.jpg
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