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Immuno-PET Imaging and Radioimmunotherapy of Lymphomas

Authors
Lee, K.-H.[Lee, K.-H.]Jung, K.-H.[Jung, K.-H.]Lee, J.H.[Lee, J.H.]
Issue Date
31-Aug-2022
Publisher
American Chemical Society
Keywords
89Zr; antibody; immuno-PET; lymphoma; radioimmunotherapy
Citation
Molecular Pharmaceutics, v.19, no.10, pp.3484 - 3491
Indexed
SCIE
SCOPUS
Journal Title
Molecular Pharmaceutics
Volume
19
Number
10
Start Page
3484
End Page
3491
URI
https://scholarworks.bwise.kr/skku/handle/2021.sw.skku/100911
DOI
10.1021/acs.molpharmaceut.2c00563
ISSN
1543-8384
Abstract
Monoclonal antibodies (Ab) have revolutionized the management of lymphomas, the most common hematologic malignancy in adults. Indeed, incorporation of rituximab into the regimen for indolent non-Hodgkin's lymphomas (NHLs) has dramatically improved treatment response and disease outcome. Yet, newer Ab therapeutics against promising antigen targets need to be developed to treat refractory or relapsed patients. Treatment efficacy can be further enhanced by conjugating toxic molecules to the Abs. Radioimmunotherapy (RIT) harnesses Abs as vehicles for targeted delivery of therapeutic radionuclide payloads for direct killing of targeted tumor cells. Positron emission tomography (PET) with radiolabeled Abs (called immuno-PET) can facilitate the development of new Ab therapeutics and RIT by providing pharmacokinetic and pharmacodynamic information and by quantifying tumor antigen level relevant for treatment decision. Immuno-PET has recently gravitated toward labeling Abs with 89Zr, a radiometal with a 3.3 day half-life that is trapped following Ab internalization and thus provides high-resolution PET images with excellent contrast. Immuno-PET methods against major lymphoma antigens including CD20 and other promising targets are currently under development. With continued improvements, immuno-PET has the potential to be used in lymphoma management as an imaging biomarker for patient selection and assessment of treatment response. © 2022 American Chemical Society.
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