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111In-贝伐单抗成像检测肾细胞癌及血管内皮生长因子受体抑制剂索拉非尼新辅助治疗的评估。

111In-bevacizumab imaging of renal cell cancer and evaluation of neoadjuvant treatment with the vascular endothelial growth factor receptor inhibitor sorafenib.

机构信息

Department of Medical Oncology, Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands.

出版信息

J Nucl Med. 2010 Nov;51(11):1707-15. doi: 10.2967/jnumed.110.078030. Epub 2010 Oct 18.

Abstract

UNLABELLED

Clear cell renal cell cancer (ccRCC) prominently expresses vascular endothelial growth factor-A (VEGF-A), and new treatment strategies for renal cell cancer (RCC) aim at the inhibition of VEGF-VEGF receptor signaling. This study explores the ability of (111)In-bevacizumab scintigraphy to depict RCC and to evaluate response to neoadjuvant treatment with sorafenib, a VEGF receptor inhibitor.

METHODS

The ability to depict RCC with (111)In-bevacizumab scintigraphy was tested in 14 patients scheduled to undergo a tumor nephrectomy; of these, 9 RCC patients were treated in a neoadjuvant setting with sorafenib (400 mg orally twice a day). In the latter group, baseline and posttreatment (111)In-bevacizumab scans were compared. The intratumoral distribution of (111)In-bevacizumab was determined scintigraphically ex vivo in a 1-cm lamella of the resected tumorous kidney. Expression of VEGF-A, glucose transporter-1, carbonic anhydrase IX, α-smooth-muscle actin, and Ki67 was determined by immunohistochemistry and compared with the local concentration of (111)In-bevacizumab. Additionally, the VEGF-A content in tumor samples was determined quantitatively by enzyme-linked immunosorbent assay.

RESULTS

In all 5 non-neoadjuvant-treated patients, preferential accumulation of (111)In-bevacizumab was observed in the tumors. All ccRCC lesions with enhanced (111)In-bevacizumab targeting expressed high levels of VEGF-A. Treatment with sorafenib resulted in a significant decrease of (111)In-bevacizumab uptake in the tumor in the patients with ccRCC (mean change, -60.5%; range, +1.5% to -90.1%). The decrease in uptake was due to destruction of the tumor neovasculature, whereas the VEGF-A expression remained intact. In the patient with papillary RCC, limited uptake without change after sorafenib was observed.

CONCLUSION

RCC lesions were clearly delineated with (111)In-bevacizumab scintigraphy. Neoadjuvant treatment with sorafenib resulted in a significant decrease of (111)In-bevacizumab uptake in RCC. (111)In-bevacizumab scintigraphy can be an attractive biomarker for response and needs further study.

摘要

目的

探索放射性核素标记贝伐单抗(111In-bevacizumab)闪烁显像探测肾细胞癌(RCC)的能力,并评估其在索拉非尼(一种血管内皮生长因子受体抑制剂)新辅助治疗中的作用。

方法

14 例行肿瘤肾切除术的患者纳入本研究;其中 9 例 RCC 患者接受索拉非尼(400 mg,每日口服 2 次)新辅助治疗。比较后者的基线和治疗后(111)In-bevacizumab 扫描结果。通过切除肾脏肿瘤的 1 cm 切片进行离体闪烁显像,确定肿瘤内 111In-bevacizumab 的分布。通过免疫组织化学方法检测血管内皮生长因子-A(VEGF-A)、葡萄糖转运蛋白-1、碳酸酐酶 IX、α-平滑肌肌动蛋白和 Ki67 的表达,并与局部 111In-bevacizumab 浓度进行比较。此外,通过酶联免疫吸附试验定量检测肿瘤样本中的 VEGF-A 含量。

结果

在所有 5 例未接受新辅助治疗的患者中,(111)In-bevacizumab 均优先在肿瘤中聚集。所有表达增强的(111)In-bevacizumab 靶向的 ccRCC 病变均表达高水平的 VEGF-A。在 ccRCC 患者中,索拉非尼治疗导致(111)In-bevacizumab 摄取显著下降(平均变化,-60.5%;范围,+1.5%至-90.1%)。摄取减少归因于肿瘤新生血管的破坏,而 VEGF-A 的表达仍然完整。在乳头状 RCC 患者中,观察到摄取有限且索拉非尼治疗后无变化。

结论

放射性核素标记贝伐单抗闪烁显像能清晰描绘 RCC 病变。索拉非尼新辅助治疗可显著降低 RCC 中 111In-bevacizumab 的摄取。(111)In-bevacizumab 闪烁显像可能是一种有吸引力的反应生物标志物,需要进一步研究。

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