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

49Citations
Citations of this article
56Readers
Mendeley users who have this article in their library.

Abstract

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 111In-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 111In-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 111In-bevacizumab scans were compared. The intratumoral distribution of 111In-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 111In-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 111In-bevacizumab was observed in the tumors. All ccRCC lesions with enhanced 111In-bevacizumab targeting expressed high levels of VEGF-A. Treatment with sorafenib resulted in a significant decrease of 111In-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 111Inbevacizumab scintigraphy. Neoadjuvant treatment with sorafenib resulted in a significant decrease of 111In-bevacizumab uptake in RCC. 111In-bevacizumab scintigraphy can be an attractive biomarker for response and needs further study. Copyright © 2010 by the Society of Nuclear Medicine, Inc.

Cite

CITATION STYLE

APA

Desar, I. M. E., Stillebroer, A. B., Oosterwijk, E., Leenders, W. P. J., Van Herpen, C. M. L., Van Der Graaf, W. T. A., … Oyen, W. J. G. (2010). 111In-bevacizumab imaging of renal cell cancer and evaluation of neoadjuvant treatment with the vascular endothelial growth factor receptor inhibitor sorafenib. Journal of Nuclear Medicine, 51(11), 1707–1715. https://doi.org/10.2967/jnumed.110.078030

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free