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使用 C-X-C 趋化因子受体 4 放射性配体靶向治疗难治性套细胞淋巴瘤的影像学和治疗。

Targeting Refractory Mantle Cell Lymphoma for Imaging and Therapy Using C-X-C Chemokine Receptor Type 4 Radioligands.

机构信息

Molecular Oncology, British Columbia Cancer, Vancouver, British Columbia, Canada.

Centre for Lymphoid Cancer, British Columbia Cancer, Vancouver, British Columbia, Canada.

出版信息

Clin Cancer Res. 2022 Apr 14;28(8):1628-1639. doi: 10.1158/1078-0432.CCR-21-3284.

Abstract

PURPOSE

Mantle cell lymphoma (MCL) is associated with poor survival. The purpose of this study was to assess whether the C-X-C chemokine receptor type 4 (CXCR4) is a useful target for imaging and radioligand therapy of MCL, using a novel pair of radioligands, [68Ga]Ga and [177Lu]Lu-BL02.

EXPERIMENTAL DESIGN

We performed a retrospective analysis of 146 patients with MCL to evaluate CXCR4 expression and its correlation with outcomes. Guided by in silico methods, we designed BL02, a new radioligand labelled with 68Ga or 177Lu for PET imaging and therapy, respectively. We performed imaging and biodistribution studies in xenograft models with varying CXCR4 expression. We evaluated [177Lu]Lu-BL02 in MCL models, and evaluated its potential for therapy in Z138 MCL xenografts.

RESULTS

Phosphorylated and nonphosphorylated CXCR4 expression were correlated with poor survival in patients with MCL and characterized by unique underlying molecular signatures. [68Ga]Ga-BL02 uptake correlated with CXCR4 expression, and localized lesions in a metastatic xenograft model. [177Lu]Lu-BL02 showed high uptake in MCL xenografts. Therapy studies with a single dose in the Z138 model showed tumor regression and improved survival compared with a control group. Upon regrowth, the treated mice experienced concurrent metastasis alongside localized xenograft regrowth, and recurrent lesions showed enhanced CXCR4 signaling.

CONCLUSIONS

CXCR4 is an independent factor of poor prognosis for MCL and a promising target for imaging and radioligand therapy. [68Ga]Ga-BL02 showed high contrast to visualize CXCR4-expressing xenografts for PET imaging and [177Lu]Lu-BL02 induced rapid tumor regression in a preclinical model of MCL.

摘要

目的

套细胞淋巴瘤(MCL)与预后不良相关。本研究旨在评估新型放射性配体[68Ga]Ga 和 [177Lu]Lu-BL02 对 MCL 成像和放射性配体治疗是否具有潜在价值,使用一种新的放射性配体,C-X-C 趋化因子受体 4(CXCR4)。

实验设计

我们对 146 例 MCL 患者进行了回顾性分析,以评估 CXCR4 表达及其与预后的相关性。根据计算机模拟方法,我们设计了 BL02,一种分别用 68Ga 或 177Lu 标记的新型放射性配体,用于 PET 成像和治疗。我们在表达不同 CXCR4 的异种移植模型中进行了成像和生物分布研究。我们评估了 MCL 模型中的 [177Lu]Lu-BL02,并评估了其在 Z138 MCL 异种移植瘤中的治疗潜力。

结果

磷酸化和非磷酸化 CXCR4 的表达与 MCL 患者的不良预后相关,并具有独特的潜在分子特征。[68Ga]Ga-BL02 的摄取与 CXCR4 的表达相关,并在转移性异种移植模型中定位病变。[177Lu]Lu-BL02 在 MCL 异种移植瘤中摄取量高。在 Z138 模型中单次剂量治疗研究显示与对照组相比,肿瘤消退和生存时间延长。在复发时,治疗小鼠同时伴有局部异种移植瘤复发和转移,且复发病变显示出增强的 CXCR4 信号。

结论

CXCR4 是 MCL 预后不良的独立因素,是成像和放射性配体治疗的有前途的靶点。[68Ga]Ga-BL02 显示出高对比度,可用于 PET 成像以可视化表达 CXCR4 的异种移植瘤,[177Lu]Lu-BL02 在 MCL 的临床前模型中诱导快速肿瘤消退。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73e2/9365342/e25820b3f318/1628fig1.jpg

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