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五聚素蛋白 PET/CT 用于食管癌趋化因子受体 4 表达成像——首次临床探索。

Pentixafor PET/CT for imaging of chemokine receptor 4 expression in esophageal cancer - a first clinical approach.

机构信息

Department of Radiation Oncology, University Hospital of Cologne, University of Cologne, Kerpener St 62, 50937, Cologne, Germany.

Department of Pathology, University Hospital of Cologne, University of Cologne, Cologne, Germany.

出版信息

Cancer Imaging. 2021 Feb 12;21(1):22. doi: 10.1186/s40644-021-00391-w.

Abstract

BACKGROUND

Expression of CXCR4, a chemokine (C-X-C motif) receptor that plays a central role in tumor growth and metastasis of circulating tumor cells, has been described in a variety of solid tumors. A high expression of CXCR4 has a prognostic significance with regard to overall and progression-free survival and offers a starting point for targeted therapies. In this context, [68]Ga-Pentixafor-Positron Emission Tomography/Computer Tomography (PET/CT) offers promising possibility of imaging the CXCR4 expression profile. We set out to compare a [18F] fluorodeoxyglucose (FDG)-PET/CT and a [68Ga]Pentixafor-PET/CT in (re-)staging and radiation planning of patients with localized esophageal cancer.

MATERIALS AND METHODS

In this retrospective analysis, ten patients, with adeno- or squamous cell carcinoma of the esophagus (n = 3 and n = 7, respectively), which were scheduled for radio (chemo) therapy, were imaged using both Pentixafor and FDG PET/CT examinations. All lesions were visually rated as Pentixafor and FDG positive or negative. For both tracers, SUVmax was measured all lesions and compared to background. Additionally, immunohistochemistry of CXCR4 was obtained in patients undergoing surgery.

RESULTS

FDG-positive tumor-suspicious lesions were detected in all patients and a total of 26 lesions were counted. The lesion-based analysis brought equal status in 14 lesions which were positive for both tracers while five lesions were FDG positive and Pentixafor negative and seven lesions were FDG negative, but Pentixafor positive. Histopathologic correlation was available in seven patients. The CXCR4 expression of four non-pretreated tumour lesion samples was confirmed immunohistochemically.

CONCLUSION

Our data shows that additional PET/CT imaging with Pentixafor for imaging the CXCR4 chemokine receptor is feasible but heterogeneous in both newly diagnosed and pretreated recurrent esophageal cancer. In addition, the Pentixafor PET/CT may serve as complementary tool for radiation field expansion in radiooncology.

摘要

背景

趋化因子(C-X-C 基序)受体 CXCR4 的表达在循环肿瘤细胞的肿瘤生长和转移中起着核心作用,已在多种实体瘤中得到描述。CXCR4 的高表达与总生存和无进展生存具有预后意义,并为靶向治疗提供了起点。在这种情况下,[68]Ga-五肽基-tetraxin 正电子发射断层扫描/计算机断层扫描(PET/CT)为成像 CXCR4 表达谱提供了有前途的可能性。我们旨在比较氟脱氧葡萄糖(FDG)-PET/CT 和[68Ga]五肽基-tetraxin-PET/CT 在局部食管癌患者的(再)分期和放射计划中的应用。

材料和方法

在这项回顾性分析中,十名患有食管腺癌或鳞状细胞癌的患者(分别为 3 名和 7 名),计划接受放射(化疗)治疗,分别进行了五肽基-tetraxin 和 FDG PET/CT 检查。所有病变均通过视觉评分判断为五肽基-tetraxin 和 FDG 阳性或阴性。对于两种示踪剂,均测量了所有病变的 SUVmax,并与背景进行了比较。此外,对接受手术的患者进行了 CXCR4 的免疫组织化学检查。

结果

所有患者均检测到 FDG 阳性的肿瘤可疑病变,共发现 26 处病变。基于病变的分析在 14 处同时对两种示踪剂均为阳性的病变中得出相同的结果,而 5 处病变 FDG 阳性而五肽基-tetraxin 阴性,7 处病变 FDG 阴性但五肽基-tetraxin 阳性。在 7 名患者中获得了组织病理学相关性。免疫组织化学证实了 4 例未经预处理的肿瘤病变样本的 CXCR4 表达。

结论

我们的数据表明,对于新诊断和复发性食管癌,使用五肽基-tetraxin 进行 CXCR4 趋化因子受体的额外 PET/CT 成像可行,但结果存在异质性。此外,五肽基-tetraxin PET/CT 可能作为放射肿瘤学中放射野扩展的补充工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fbf5/7881561/989dfe3f6374/40644_2021_391_Fig1_HTML.jpg

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