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基于 5-甲基四氢叶酸的放射性缀合物的临床前评估——叶酸受体靶向放射性核素治疗的新视角。

Preclinical evaluation of 5-methyltetrahydrofolate-based radioconjugates-new perspectives for folate receptor-targeted radionuclide therapy.

机构信息

Center for Radiopharmaceutical Sciences ETH-PSI-USZ, Paul Scherrer Institute - PSI, 5232, Villigen-PSI, Switzerland.

Department of Chemistry and Applied Biosciences, ETH Zurich, 8093, Zurich, Switzerland.

出版信息

Eur J Nucl Med Mol Imaging. 2021 Apr;48(4):972-983. doi: 10.1007/s00259-020-04980-y. Epub 2020 Oct 15.

Abstract

PURPOSE

The folate receptor (FR) is frequently overexpressed in a variety of tumor types and, hence, an interesting target for radionuclide therapy. The aim of this study was to evaluate a new class of albumin-binding radioconjugates comprising 5-methyltetrahydrofolate (5-MTHF) as a targeting agent and to compare their properties with those of the previously established folic acid-based [Lu]Lu-OxFol-1.

METHODS

[Lu]Lu-6R-RedFol-1 and [Lu]Lu-6S-RedFol-1 were investigated in vitro using FR-positive KB tumor cells. Biodistribution studies were performed in KB tumor-bearing mice, and the areas under the curve (AUC) were determined for the uptake in tumors and kidneys. [Lu]Lu-6R-RedFol-1 was compared with [Lu]Lu-OxFol-1 in a therapy study over 8 weeks using KB tumor-bearing mice.

RESULTS

Both radioconjugates demonstrated similar in vitro properties as [Lu]Lu-OxFol-1; however, the tumor uptake of [Lu]Lu-6R-RedFol-1 and [Lu]Lu-6S-RedFol-1 was significantly increased in comparison with [Lu]Lu-OxFol-1. In the case of [Lu]Lu-6S-RedFol-1, also the kidney uptake was increased; however, renal retention of [Lu]Lu-6R-RedFol-1 was similar to that of [Lu]Lu-OxFol-1. This led to an almost 4-fold increased tumor-to-kidney AUC ratio of [Lu]Lu-6R-RedFol-1 as compared with [Lu]Lu-6S-RedFol-1 and [Lu]Lu-OxFol-1. At equal activity, the therapeutic effect of [Lu]Lu-6R-RedFol-1 was better than that of [Lu]Lu-OxFol-1, reflected by a slower tumor growth and, consequently, an increased median survival time (49 days vs. 34 days).

CONCLUSION

This study demonstrated the promising potential of 5-MTHF-based radioconjugates for FR-targeting. Application of [Lu]Lu-6R-RedFol-1 resulted in unprecedentedly high tumor-to-kidney ratios and, as a consequence, a superior therapeutic effect as compared with [Lu]Lu-OxFol-1. These findings, together with the absence of early side effects, make [Lu]Lu-6R-RedFol-1 attractive in view of a future clinical translation.

摘要

目的

叶酸受体(FR)在多种肿瘤类型中过度表达,因此是放射性核素治疗的一个有趣靶点。本研究的目的是评估一类新的白蛋白结合放射性缀合物,其包含 5-甲基四氢叶酸(5-MTHF)作为靶向剂,并将其性质与先前建立的叶酸基[Lu]Lu-OxFol-1 进行比较。

方法

使用 FR 阳性 KB 肿瘤细胞在体外研究[Lu]Lu-6R-RedFol-1 和 [Lu]Lu-6S-RedFol-1。在 KB 肿瘤荷瘤小鼠中进行了生物分布研究,并确定了肿瘤和肾脏摄取的曲线下面积(AUC)。在使用 KB 肿瘤荷瘤小鼠的 8 周治疗研究中,将 [Lu]Lu-6R-RedFol-1 与 [Lu]Lu-OxFol-1 进行了比较。

结果

两种放射性缀合物在体外均表现出与 [Lu]Lu-OxFol-1 相似的性质;然而,与 [Lu]Lu-OxFol-1 相比,[Lu]Lu-6R-RedFol-1 和 [Lu]Lu-6S-RedFol-1 的肿瘤摄取明显增加。对于 [Lu]Lu-6S-RedFol-1,肾脏摄取也增加;然而,[Lu]Lu-6R-RedFol-1 的肾脏保留与 [Lu]Lu-OxFol-1 相似。这导致与 [Lu]Lu-6S-RedFol-1 和 [Lu]Lu-OxFol-1 相比,[Lu]Lu-6R-RedFol-1 的肿瘤-肾脏 AUC 比值几乎增加了 4 倍。在相等的活性下,[Lu]Lu-6R-RedFol-1 的治疗效果优于 [Lu]Lu-OxFol-1,这反映在肿瘤生长较慢,因此中位生存时间延长(49 天比 34 天)。

结论

本研究证明了基于 5-MTHF 的放射性缀合物用于 FR 靶向的有前途的潜力。应用 [Lu]Lu-6R-RedFol-1 导致前所未有的肿瘤-肾脏比值,并因此与 [Lu]Lu-OxFol-1 相比具有更好的治疗效果。这些发现,以及没有早期副作用,使得 [Lu]Lu-6R-RedFol-1 具有未来临床转化的吸引力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/08b4/8041685/49538d370b1b/259_2020_4980_Fig1_HTML.jpg

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