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First In-Human Medical Imaging with a PASylated (89)Zr-Labeled Anti-HER2 Fab-Fragment in a Patient with Metastatic Breast Cancer
PURPOSE: PASylation® offers the ability to systematically tune and optimize the pharmacokinetics of protein tracers for molecular imaging. Here we report the first clinical translation of a PASylated Fab fragment ((89)Zr∙Df-HER2-Fab-PAS(200)) for the molecular imaging of tumor-related HER2 expressio...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Singapore
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7198682/ https://www.ncbi.nlm.nih.gov/pubmed/32377263 http://dx.doi.org/10.1007/s13139-020-00638-7 |
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author | Richter, Antonia Knorr, Karina Schlapschy, Martin Robu, Stephanie Morath, Volker Mendler, Claudia Yen, Hsi-Yu Steiger, Katja Kiechle, Marion Weber, Wolfgang Skerra, Arne Schwaiger, Markus |
author_facet | Richter, Antonia Knorr, Karina Schlapschy, Martin Robu, Stephanie Morath, Volker Mendler, Claudia Yen, Hsi-Yu Steiger, Katja Kiechle, Marion Weber, Wolfgang Skerra, Arne Schwaiger, Markus |
author_sort | Richter, Antonia |
collection | PubMed |
description | PURPOSE: PASylation® offers the ability to systematically tune and optimize the pharmacokinetics of protein tracers for molecular imaging. Here we report the first clinical translation of a PASylated Fab fragment ((89)Zr∙Df-HER2-Fab-PAS(200)) for the molecular imaging of tumor-related HER2 expression. METHODS: A patient with HER2-positive metastatic breast cancer received 37 MBq of (89)Zr∙Df-HER2-Fab-PAS(200) at a total mass dose of 70 μg. PET/CT was carried out 6, 24, and 45 h after injection, followed by image analysis of biodistribution, normal organ uptake, and lesion targeting. RESULTS: Images show a biodistribution typical for protein tracers, characterized by a prominent blood pool 6 h p.i., which decreased over time. Lesions were detectable as early as 24 h p.i. (89)Zr∙Df-HER2-Fab-PAS(200) was tolerated well. CONCLUSION: This study demonstrates that a PASylated Fab tracer shows appropriate blood clearance to allow sensitive visualization of small tumor lesions in a clinical setting. |
format | Online Article Text |
id | pubmed-7198682 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Springer Singapore |
record_format | MEDLINE/PubMed |
spelling | pubmed-71986822020-05-06 First In-Human Medical Imaging with a PASylated (89)Zr-Labeled Anti-HER2 Fab-Fragment in a Patient with Metastatic Breast Cancer Richter, Antonia Knorr, Karina Schlapschy, Martin Robu, Stephanie Morath, Volker Mendler, Claudia Yen, Hsi-Yu Steiger, Katja Kiechle, Marion Weber, Wolfgang Skerra, Arne Schwaiger, Markus Nucl Med Mol Imaging Original Article PURPOSE: PASylation® offers the ability to systematically tune and optimize the pharmacokinetics of protein tracers for molecular imaging. Here we report the first clinical translation of a PASylated Fab fragment ((89)Zr∙Df-HER2-Fab-PAS(200)) for the molecular imaging of tumor-related HER2 expression. METHODS: A patient with HER2-positive metastatic breast cancer received 37 MBq of (89)Zr∙Df-HER2-Fab-PAS(200) at a total mass dose of 70 μg. PET/CT was carried out 6, 24, and 45 h after injection, followed by image analysis of biodistribution, normal organ uptake, and lesion targeting. RESULTS: Images show a biodistribution typical for protein tracers, characterized by a prominent blood pool 6 h p.i., which decreased over time. Lesions were detectable as early as 24 h p.i. (89)Zr∙Df-HER2-Fab-PAS(200) was tolerated well. CONCLUSION: This study demonstrates that a PASylated Fab tracer shows appropriate blood clearance to allow sensitive visualization of small tumor lesions in a clinical setting. Springer Singapore 2020-04-20 2020-04 /pmc/articles/PMC7198682/ /pubmed/32377263 http://dx.doi.org/10.1007/s13139-020-00638-7 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Original Article Richter, Antonia Knorr, Karina Schlapschy, Martin Robu, Stephanie Morath, Volker Mendler, Claudia Yen, Hsi-Yu Steiger, Katja Kiechle, Marion Weber, Wolfgang Skerra, Arne Schwaiger, Markus First In-Human Medical Imaging with a PASylated (89)Zr-Labeled Anti-HER2 Fab-Fragment in a Patient with Metastatic Breast Cancer |
title | First In-Human Medical Imaging with a PASylated (89)Zr-Labeled Anti-HER2 Fab-Fragment in a Patient with Metastatic Breast Cancer |
title_full | First In-Human Medical Imaging with a PASylated (89)Zr-Labeled Anti-HER2 Fab-Fragment in a Patient with Metastatic Breast Cancer |
title_fullStr | First In-Human Medical Imaging with a PASylated (89)Zr-Labeled Anti-HER2 Fab-Fragment in a Patient with Metastatic Breast Cancer |
title_full_unstemmed | First In-Human Medical Imaging with a PASylated (89)Zr-Labeled Anti-HER2 Fab-Fragment in a Patient with Metastatic Breast Cancer |
title_short | First In-Human Medical Imaging with a PASylated (89)Zr-Labeled Anti-HER2 Fab-Fragment in a Patient with Metastatic Breast Cancer |
title_sort | first in-human medical imaging with a pasylated (89)zr-labeled anti-her2 fab-fragment in a patient with metastatic breast cancer |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7198682/ https://www.ncbi.nlm.nih.gov/pubmed/32377263 http://dx.doi.org/10.1007/s13139-020-00638-7 |
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