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FLT-PET for early response evaluation of colorectal cancer patients with liver metastases: a prospective study

BACKGROUND: Fluoro-L-thymidine (FLT) is a positron emission tomography/computed tomography (PET/CT) tracer which reflects proliferative activity in a cancer lesion. The main objective of this prospective explorative study was to evaluate whether FLT-PET can be used for the early evaluation of treatm...

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Autores principales: Mogensen, Marie Benzon, Loft, Annika, Aznar, Marianne, Axelsen, Thomas, Vainer, Ben, Osterlind, Kell, Kjaer, Andreas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5503853/
https://www.ncbi.nlm.nih.gov/pubmed/28695424
http://dx.doi.org/10.1186/s13550-017-0302-3
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author Mogensen, Marie Benzon
Loft, Annika
Aznar, Marianne
Axelsen, Thomas
Vainer, Ben
Osterlind, Kell
Kjaer, Andreas
author_facet Mogensen, Marie Benzon
Loft, Annika
Aznar, Marianne
Axelsen, Thomas
Vainer, Ben
Osterlind, Kell
Kjaer, Andreas
author_sort Mogensen, Marie Benzon
collection PubMed
description BACKGROUND: Fluoro-L-thymidine (FLT) is a positron emission tomography/computed tomography (PET/CT) tracer which reflects proliferative activity in a cancer lesion. The main objective of this prospective explorative study was to evaluate whether FLT-PET can be used for the early evaluation of treatment response in colorectal cancer patients (CRC) with liver metastases. Patients with metastatic CRC having at least one measurable (>1 cm) liver metastasis receiving first-line chemotherapy were included. A FLT-PET/CT scan was performed at baseline and after the first treatment. The maximum and mean standardised uptake values (SUV(max), SUV(mean)) were measured. After three cycles of chemotherapy, treatment response was assessed by CT scan based on RECIST 1.1. RESULTS: Thirty-nine consecutive patients were included of which 27 were evaluable. Dropout was mainly due to disease complications. Nineteen patients (70%) had a partial response, seven (26%) had stable disease and one (4%) had progressive disease. A total of 23 patients (85%) had a decrease in FLT uptake following the first treatment. The patient with progressive disease had the highest increase in FLT uptake in SUV(max). There was no correlation between the response according to RECIST and the early changes in FLT uptake measured as SUV(max) (p = 0.24). CONCLUSIONS: No correlation was found between early changes in FLT uptake after the first cycle of treatment and the response evaluated from subsequent CT scans. It seems unlikely that FLT-PET can be used on its own for the early response evaluation of metastatic CRC.
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spelling pubmed-55038532017-07-25 FLT-PET for early response evaluation of colorectal cancer patients with liver metastases: a prospective study Mogensen, Marie Benzon Loft, Annika Aznar, Marianne Axelsen, Thomas Vainer, Ben Osterlind, Kell Kjaer, Andreas EJNMMI Res Original Research BACKGROUND: Fluoro-L-thymidine (FLT) is a positron emission tomography/computed tomography (PET/CT) tracer which reflects proliferative activity in a cancer lesion. The main objective of this prospective explorative study was to evaluate whether FLT-PET can be used for the early evaluation of treatment response in colorectal cancer patients (CRC) with liver metastases. Patients with metastatic CRC having at least one measurable (>1 cm) liver metastasis receiving first-line chemotherapy were included. A FLT-PET/CT scan was performed at baseline and after the first treatment. The maximum and mean standardised uptake values (SUV(max), SUV(mean)) were measured. After three cycles of chemotherapy, treatment response was assessed by CT scan based on RECIST 1.1. RESULTS: Thirty-nine consecutive patients were included of which 27 were evaluable. Dropout was mainly due to disease complications. Nineteen patients (70%) had a partial response, seven (26%) had stable disease and one (4%) had progressive disease. A total of 23 patients (85%) had a decrease in FLT uptake following the first treatment. The patient with progressive disease had the highest increase in FLT uptake in SUV(max). There was no correlation between the response according to RECIST and the early changes in FLT uptake measured as SUV(max) (p = 0.24). CONCLUSIONS: No correlation was found between early changes in FLT uptake after the first cycle of treatment and the response evaluated from subsequent CT scans. It seems unlikely that FLT-PET can be used on its own for the early response evaluation of metastatic CRC. Springer Berlin Heidelberg 2017-07-10 /pmc/articles/PMC5503853/ /pubmed/28695424 http://dx.doi.org/10.1186/s13550-017-0302-3 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Original Research
Mogensen, Marie Benzon
Loft, Annika
Aznar, Marianne
Axelsen, Thomas
Vainer, Ben
Osterlind, Kell
Kjaer, Andreas
FLT-PET for early response evaluation of colorectal cancer patients with liver metastases: a prospective study
title FLT-PET for early response evaluation of colorectal cancer patients with liver metastases: a prospective study
title_full FLT-PET for early response evaluation of colorectal cancer patients with liver metastases: a prospective study
title_fullStr FLT-PET for early response evaluation of colorectal cancer patients with liver metastases: a prospective study
title_full_unstemmed FLT-PET for early response evaluation of colorectal cancer patients with liver metastases: a prospective study
title_short FLT-PET for early response evaluation of colorectal cancer patients with liver metastases: a prospective study
title_sort flt-pet for early response evaluation of colorectal cancer patients with liver metastases: a prospective study
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5503853/
https://www.ncbi.nlm.nih.gov/pubmed/28695424
http://dx.doi.org/10.1186/s13550-017-0302-3
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