Title
<tex>$^{18}F-FDG$</tex> and <tex>$^{18}F-FLT$</tex> uptake early after cyclophosphamide and mTOR inhibition in an experimental lymphoma model <tex>$^{18}F-FDG$</tex> and <tex>$^{18}F-FLT$</tex> uptake early after cyclophosphamide and mTOR inhibition in an experimental lymphoma model
Author
Faculty/Department
Faculty of Medicine and Health Sciences
Publication type
article
Publication
New York ,
Subject
Human medicine
Source (journal)
The Journal of nuclear medicine. - New York
Volume/pages
50(2009) :7 , p. 1102-1109
ISSN
0161-5505
Carrier
E
Target language
English (eng)
Full text (Publishers DOI)
Abstract
To be a reliable predictor of response, tracer uptake should reflect changes in the amount of active tumor cells. However, uptake of 18F-FDG, the most commonly used PET tracer, is disturbed by the inflammatory cells that appear early after cytotoxic therapy. The first aim of this study was to investigate whether 3′-18F-fluoro-3′-deoxy-l-thymidine (18F-FLT), a marker of cellular proliferation, is a better tracer for response assessment early after cytotoxic therapy. A second objective of this study was to investigate whether 18F-FDG and 18F-FLT responses were comparable early after mammalian target of rapamycin (mTOR) inhibition, as an example of proliferation-targeting therapies. Methods: Severe combined immunodeficient mice were subcutaneously inoculated with Granta-519 cells, a human cell line derived from a leukemic mantle cell lymphoma. Half the mice were treated with cyclophosphamide and the other half with mTOR inhibition. 18F-FDG and 18F-FLT uptake was evaluated by small-animal PET on day 0 (D0; before treatment), D+1, D+2, D+4, D+7, D+9, D+11, and D+14. At each time point, 2 mice of each treatment condition were sacrificed, and tumors were excised for histopathology. Results: After cyclophosphamide, 18F-FDG and 18F-FLT uptake decreased, with a maximum reduction of −29% for 18F-FDG and −25% for 18F-FLT uptake at D+2, compared with baseline. Although 18F-FDG uptake increased from D+4 on, with a maximum on D+7, 18F-FLT uptake remained virtually stable. Histology showed an increase in apoptotic or necrotic tumor fraction, followed by an influx of inflammatory cells. In mTOR-inhibited mice, 18F-FDG uptake dropped until D+2 after therapy (−43%) but increased at D+4 (−27%) to form a plateau on D+7 and D+9 (−14% and −16%, respectively). Concurrently, 18F-FLT uptake decreased to −31% on D+2, followed by an increase with a peak value of +12% on D+7, after which 18F-FLT uptake decreased again. Cyclin D1 expression dropped from D+1 until D+4 and returned to baseline at D+7. Conclusion: Because 18F-FLT uptake is not significantly influenced by the temporary rise in inflammatory cells early after cyclophosphamide, it more accurately reflects tumor response. However, a formerly unknown temporary rise in 18F-FLT uptake a few days after the administration of mTOR inhibition was defined, which makes it clear that drug-specific responses have to be considered when using PET for early treatment monitoring.
E-info
https://repository.uantwerpen.be/docman/iruaauth/c55d3c/3ab56eb07c3.pdf