Department of Medical Oncology, Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands.
J Nucl Med. 2010 Nov;51(11):1707-15. doi: 10.2967/jnumed.110.078030. Epub 2010 Oct 18.
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.
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.
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.
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.
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。
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。
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。
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。