MRI Assessment of Changes in Tumor Vascularization during Neoadjuvant Anti-Angiogenic Treatment in Locally Advanced Breast Cancer Patients

Author:

Mo Torgeir12ORCID,Brandal Siri Helene Bertelsen13ORCID,Geier Oliver Marcel4ORCID,Engebråten Olav156,Nilsen Line Brennhaug7,Kristensen Vessela N.18,Hole Knut Håkon19,Hompland Tord10,Fleischer Thomas2ORCID,Seierstad Therese11ORCID

Affiliation:

1. Faculty of Clinical Medicine, University of Oslo, 0316 Oslo, Norway

2. Department of Cancer Genetics, Institute for Cancer Research, Oslo University Hospital, 4950 Oslo, Norway

3. Department of Breast Diagnostic, Oslo University Hospital, 0379 Oslo, Norway

4. Department of Diagnostic Physics, Oslo University Hospital, 0379 Oslo, Norway

5. Department of Oncology, Oslo University Hospital, 0379 Oslo, Norway

6. Department of Tumor Biology, Institute for Cancer Research, Oslo University Hospital, 4950 Oslo, Norway

7. Department of Medical Physics, Oslo University Hospital, 0379 Oslo, Norway

8. Department of Medical Genetics, Oslo University Hospital, 0450 Oslo, Norway

9. Department of Oncologic Radiology, Division of Radiology and Nuclear Medicine, Oslo University Hospital, 0379 Oslo, Norway

10. Department of Radiation Biology, Oslo University Hospital, 4950 Oslo, Norway

11. Department of Research and Development, Division for Radiology and Nuclear Medicine, Oslo University Hospital, 0379 Oslo, Norway

Abstract

Anti-VEGF (vascular endothelial growth factor) treatment improves response rates, but not progression-free or overall survival in advanced breast cancer. It has been suggested that subgroups of patients may benefit from this treatment; however, the effects of adding anti-VEGF treatment to a standard chemotherapy regimen in breast cancer patients are not well studied. Understanding the effects of the anti-vascular treatment on tumor vasculature may provide a selection of patients that can benefit. The aim of this study was to study the vascular effect of bevacizumab using clinical dynamic contrast-enhanced MRI (DCE-MRI). A total of 70 women were randomized to receive either chemotherapy alone or chemotherapy with bevacizumab for 25 weeks. DCE-MRI was performed at baseline and at 12 and 25 weeks, and in addition 25 of 70 patients agreed to participate in an early MRI after one week. Voxel-wise pharmacokinetic analysis was performed using semi-quantitative methods and the extended Tofts model. Vascular architecture was assessed by calculating the fractal dimension of the contrast-enhanced images. Changes during treatment were compared with baseline and between the treatment groups. There was no significant difference in tumor volume at any point; however, DCE-MRI parameters revealed differences in vascular function and vessel architecture. Adding bevacizumab to chemotherapy led to a pronounced reduction in vascular DCE-MRI parameters, indicating decreased vascularity. At 12 and 25 weeks, the difference between the treatment groups is severely reduced.

Funder

convergence environment grant PerCaThe

Publisher

MDPI AG

Subject

Cancer Research,Oncology

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