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Comparative biodistribution analysis across four different 89 Zr-monoclonal antibody tracers-The first step towards an imaging warehouse.

Authors :
Bensch F
Smeenk MM
van Es SC
de Jong JR
Schröder CP
Oosting SF
Lub-de Hooge MN
Menke-van der Houven van Oordt CW
Brouwers AH
Boellaard R
de Vries EGE
Source :
Theranostics [Theranostics] 2018 Jul 30; Vol. 8 (16), pp. 4295-4304. Date of Electronic Publication: 2018 Jul 30 (Print Publication: 2018).
Publication Year :
2018

Abstract

Rationale: Knowledge on monoclonal antibody biodistribution in healthy tissues in humans can support clinical drug development. Molecular imaging with positron emission tomography (PET) can yield information in this setting. However, recent imaging studies have analyzed the behavior of single antibodies only, neglecting comparison across different antibodies. Methods: We compared the distribution of four <superscript>89</superscript> Zr-labeled antibodies in healthy tissue in a retrospective analysis based on the recently published harmonization protocol for <superscript>89</superscript> Zr-tracers and our delineation protocol. Results: The biodistribution patterns of <superscript>89</superscript> Zr-lumretuzumab, <superscript>89</superscript> Zr-MMOT0530A, <superscript>89</superscript> Zr-bevacizumab and <superscript>89</superscript> Zr-trastuzumab on day 4 after tracer injection were largely similar. The highest tracer concentration was seen in healthy liver, spleen, kidney and intestines. About one-third of the injected tracer dose was found in the circulation, up to 15% in the liver and only 4% in the spleen and kidney. Lower tracer concentration was seen in bone marrow, lung, compact bone, muscle, fat and the brain. Despite low tracer accumulation per gram of tissue, large-volume tissues, especially fat, can influence overall distribution: On average, 5-7% of the injected tracer dose accumulated in fat, with a peak of 19% in a patient with morbid obesity. Conclusion: The similar biodistribution of the four antibodies is probably based on their similar molecular structure, binding characteristics and similar metabolic pathways. These data provide a basis for a prospectively growing, online accessible warehouse of molecular imaging data, which enables researchers to increase and exchange knowledge on whole body drug distribution and potentially supports drug development decisions.<br />Competing Interests: Competing Interests: The UMCG received grants form Roche and Genentech for conduct of the imaging trials. All other authors declare no competing interests.

Details

Language :
English
ISSN :
1838-7640
Volume :
8
Issue :
16
Database :
MEDLINE
Journal :
Theranostics
Publication Type :
Academic Journal
Accession number :
30214621
Full Text :
https://doi.org/10.7150/thno.26370