Low-level whole-brain radiation enhances theranostic potential of single-domain antibody fragments for human epidermal growth factor receptor type 2 (HER2)-positive brain metastases

Daniele Procissi; Stephen A Jannetti; Markella Zannikou; Zhengyuan Zhou; Darryl McDougald; Deepak Kanojia; Hui Zhang; Kirsten Burdett; Ganesan Vaidyanathan; Michael R Zalutsky; Irina V Balyasnikova

doi:10.1093/noajnl/vdac135

Low-level whole-brain radiation enhances theranostic potential of single-domain antibody fragments for human epidermal growth factor receptor type 2 (HER2)-positive brain metastases

Neurooncol Adv. 2022 Aug 23;4(1):vdac135. doi: 10.1093/noajnl/vdac135. eCollection 2022 Jan-Dec.

Affiliations

¹ Department of Neurological Surgery, Northwestern University, Chicago, Illinois, USA.
² Department of Radiology, Duke University Medical Center, Durham, North Carolina, USA.
³ Department of Preventive Medicine, Northwestern University, Chicago, Illinois, USA.

Abstract

Background: Single-domain antibody fragments (aka V_HH, ~ 13 kDa) are promising delivery systems for brain tumor theranostics; however, achieving efficient delivery of V_HH to intracranial lesions remains challenging due to the tumor-brain barrier. Here, we evaluate low-dose whole-brain irradiation as a strategy to increase the delivery of an anti- human epidermal growth factor receptor type 2 (HER2) V_HH to breast cancer-derived intracranial tumors in mice.

Methods: Mice with intracranial HER2-positive BT474BrM3 tumors received 10-Gy fractionated cranial irradiation and were evaluated by noninvasive imaging. Anti-HER2 V_HH 5F7 was labeled with ¹⁸F, administered intravenously to irradiated mice and controls, and PET/CT imaging was conducted periodically after irradiation. Tumor uptake of ¹⁸F-labeled 5F7 in irradiated and control mice was compared by PET/CT image analysis and correlated with tumor volumes. In addition, longitudinal dynamic contrast-enhanced MRI (DCE-MRI) was conducted to visualize and quantify the potential effects of radiation on tumor perfusion and permeability.

Results: Increased ¹⁸F-labeled 5F7 intracranial tumor uptake was observed with PET in mice receiving cranial irradiation, with maximum tumor accumulation seen approximately 12 days post initial radiation treatment. No radiation-induced changes in HER2 expression were detected by Western blot, flow cytometry, or on tissue sections. DCE-MRI imaging demonstrated transiently increased tumor perfusion and permeability after irradiation, consistent with the higher tumor uptake of ¹⁸F-labeled anti-HER2 5F7 in irradiated mice.

Conclusion: Low-level brain irradiation induces dynamic changes in tumor vasculature that increase the intracranial tumor delivery of an anti-HER2 V_HH, which could facilitate the use of radiolabeled V_HH to detect, monitor, and treat HER2-expressing brain metastases.

Keywords: HER2; PET; VHH; breast cancer brain metastases; single-domain antibody fragment.