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Otto C. Boerman

Researcher at Radboud University Nijmegen

Publications -  358
Citations -  17532

Otto C. Boerman is an academic researcher from Radboud University Nijmegen. The author has contributed to research in topics: Radioimmunotherapy & In vivo. The author has an hindex of 66, co-authored 355 publications receiving 15882 citations. Previous affiliations of Otto C. Boerman include Radboud University Nijmegen Medical Centre.

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Imaging of Human Epidermal Growth Factor Receptor Type 2 Expression with 18F-Labeled Affibody Molecule ZHER2:2395 in a Mouse Model for Ovarian Cancer

TL;DR: 18F-NOTA-ZHER2:2395 is a promising new imaging agent for HER2 expression in tumors, and further research is needed to determine whether this technique can be used for patient selection for Her2-targeted therapy.
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Pretargeting of renal cell carcinoma: improved tumor targeting with a bivalent chelate.

TL;DR: Two studies indicate that the use of bivalent chelates can very effectively optimize two-step targeting of tumors with bsmAbs and indicate that this approach could optimize radioimmunotherapy.
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Early identification of antigen-specific immune responses in vivo by [18F]-labeled 3'-fluoro-3'-deoxy-thymidine ([18F]FLT) PET imaging.

TL;DR: [18F]FLT PET offers a sensitive tool to study the kinetics, localization, and involvement of lymphocyte subsets in response to vaccination and allows for early discrimination of responding from nonresponding patients in anti-cancer vaccination and aid physicians in individualized decisionmaking.
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Comparative immunohistochemical study of four monoclonal antibodies directed against ovarian carcinoma-associated antigens

TL;DR: The monoclonal antibodies OC 125, OV-TL 3, MOv 18, and Ov-TL 23, which are directed against distinct ovarian carcinoma-associated antigens, are assessed in the present study for their diagnostic value.
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Innovations in Radiotherapy Planning of Head and Neck Cancers: Role of PET

TL;DR: The current role of PET and perspectives on its future use for selection and delineation of radiotherapy target volumes and for biologic characterization of this tumor entity are described.