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.

dc.contributor.author

Procissi, Daniele

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Jannetti, Stephen A

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Zannikou, Markella

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Zhou, Zhengyuan

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McDougald, Darryl

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Kanojia, Deepak

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Zhang, Hui

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Burdett, Kirsten

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Vaidyanathan, Ganesan

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Zalutsky, Michael R

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Balyasnikova, Irina V

dc.date.accessioned

2022-10-01T15:27:56Z

dc.date.available

2022-10-01T15:27:56Z

dc.date.issued

2022-01

dc.date.updated

2022-10-01T15:27:41Z

dc.description.abstract

Background

Single-domain antibody fragments (aka VHH, ~ 13 kDa) are promising delivery systems for brain tumor theranostics; however, achieving efficient delivery of VHH 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) VHH 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 VHH 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 VHH, which could facilitate the use of radiolabeled VHH to detect, monitor, and treat HER2-expressing brain metastases.
dc.identifier

vdac135

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2632-2498

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2632-2498

dc.identifier.uri

https://hdl.handle.net/10161/25980

dc.language

eng

dc.publisher

Oxford University Press (OUP)

dc.relation.ispartof

Neuro-oncology advances

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10.1093/noajnl/vdac135

dc.subject

HER2

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PET

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VHH

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breast cancer brain metastases

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single-domain antibody fragment

dc.title

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.

dc.type

Journal article

duke.contributor.orcid

Vaidyanathan, Ganesan|0000-0003-3041-8275

duke.contributor.orcid

Zalutsky, Michael R|0000-0002-5456-0324

pubs.begin-page

vdac135

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1

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Duke

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School of Medicine

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Clinical Science Departments

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Institutes and Centers

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Pathology

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Radiation Oncology

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Radiology

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Duke Cancer Institute

pubs.publication-status

Published

pubs.volume

4

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