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Treatment outcome after radiochemotherapy in anal cancer patients staged with (18)F-FDG-PET-CT

BACKGROUND: Anal cancer (AC) is a malignancy with increasing incidence and commonly treated with radiochemotherapy. Positron-emission tomography-computed tomography (PET/CT) has been shown to improve treatment outcome in various oncological diseases, however, for AC long-term outcome data is sparse....

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Autores principales: Braun, L.H., Reinert, C.P., Zips, D., Nikolaou, K., Pfannenberg, C., Gani, C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7334798/
https://www.ncbi.nlm.nih.gov/pubmed/32642564
http://dx.doi.org/10.1016/j.ctro.2020.06.008
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author Braun, L.H.
Reinert, C.P.
Zips, D.
Nikolaou, K.
Pfannenberg, C.
Gani, C.
author_facet Braun, L.H.
Reinert, C.P.
Zips, D.
Nikolaou, K.
Pfannenberg, C.
Gani, C.
author_sort Braun, L.H.
collection PubMed
description BACKGROUND: Anal cancer (AC) is a malignancy with increasing incidence and commonly treated with radiochemotherapy. Positron-emission tomography-computed tomography (PET/CT) has been shown to improve treatment outcome in various oncological diseases, however, for AC long-term outcome data is sparse. The aim of the present study is therefore to report outcomes in our cohort of PET/CT staged AC patients treated with radiochemotherapy. METHODS: Patients with AC who were treated with radiochemotherapy in curative intent were included in this retrospective study if a PET/CT scan was performed pre-therapeutically. Information from PET/CT was considered for nodal and primary target volume definition. Radiotherapy dose to the primary tumor was 50–66 Gy and concomitant chemotherapy included 5-fluorouracil and mitomycin-C. The uptake of (18)F-fluorodeoxyglucose (FDG) was quantified using 50%-isocontour volumes of interests (VOIs) and measuring the standardized uptake value (SUV) and the metabolic tumor volume (MTV).(18)F-FDG uptake was correlated with baseline clinical parameters and long-term oncological outcome. Survival estimates were determined according to Kaplan-Meier. RESULTS: A total of 60 patients were included in this study. Estimates for three-year overall survival (OS) and disease free survival (DFS) were 94.5% and 80%. Five patients developed local (n = 2) or locoregional and local (n = 3) failure. Baseline PET/CT related parameters correlated with primary tumor stage, nodal stage and tumor grading. DFS was independent of T-stage, N-stage and baseline (18)F-FDG-uptake. CONCLUSION: In this cohort of PET/CT staged AC patients, excellent outcomes for DFS were seen. PET-based markers of tumor burden correlate with local stage of AC, however, are not of prognostic relevance for disease-free survival.
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spelling pubmed-73347982020-07-07 Treatment outcome after radiochemotherapy in anal cancer patients staged with (18)F-FDG-PET-CT Braun, L.H. Reinert, C.P. Zips, D. Nikolaou, K. Pfannenberg, C. Gani, C. Clin Transl Radiat Oncol Article BACKGROUND: Anal cancer (AC) is a malignancy with increasing incidence and commonly treated with radiochemotherapy. Positron-emission tomography-computed tomography (PET/CT) has been shown to improve treatment outcome in various oncological diseases, however, for AC long-term outcome data is sparse. The aim of the present study is therefore to report outcomes in our cohort of PET/CT staged AC patients treated with radiochemotherapy. METHODS: Patients with AC who were treated with radiochemotherapy in curative intent were included in this retrospective study if a PET/CT scan was performed pre-therapeutically. Information from PET/CT was considered for nodal and primary target volume definition. Radiotherapy dose to the primary tumor was 50–66 Gy and concomitant chemotherapy included 5-fluorouracil and mitomycin-C. The uptake of (18)F-fluorodeoxyglucose (FDG) was quantified using 50%-isocontour volumes of interests (VOIs) and measuring the standardized uptake value (SUV) and the metabolic tumor volume (MTV).(18)F-FDG uptake was correlated with baseline clinical parameters and long-term oncological outcome. Survival estimates were determined according to Kaplan-Meier. RESULTS: A total of 60 patients were included in this study. Estimates for three-year overall survival (OS) and disease free survival (DFS) were 94.5% and 80%. Five patients developed local (n = 2) or locoregional and local (n = 3) failure. Baseline PET/CT related parameters correlated with primary tumor stage, nodal stage and tumor grading. DFS was independent of T-stage, N-stage and baseline (18)F-FDG-uptake. CONCLUSION: In this cohort of PET/CT staged AC patients, excellent outcomes for DFS were seen. PET-based markers of tumor burden correlate with local stage of AC, however, are not of prognostic relevance for disease-free survival. Elsevier 2020-06-18 /pmc/articles/PMC7334798/ /pubmed/32642564 http://dx.doi.org/10.1016/j.ctro.2020.06.008 Text en © 2020 Published by Elsevier B.V. on behalf of European Society for Radiotherapy and Oncology. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Braun, L.H.
Reinert, C.P.
Zips, D.
Nikolaou, K.
Pfannenberg, C.
Gani, C.
Treatment outcome after radiochemotherapy in anal cancer patients staged with (18)F-FDG-PET-CT
title Treatment outcome after radiochemotherapy in anal cancer patients staged with (18)F-FDG-PET-CT
title_full Treatment outcome after radiochemotherapy in anal cancer patients staged with (18)F-FDG-PET-CT
title_fullStr Treatment outcome after radiochemotherapy in anal cancer patients staged with (18)F-FDG-PET-CT
title_full_unstemmed Treatment outcome after radiochemotherapy in anal cancer patients staged with (18)F-FDG-PET-CT
title_short Treatment outcome after radiochemotherapy in anal cancer patients staged with (18)F-FDG-PET-CT
title_sort treatment outcome after radiochemotherapy in anal cancer patients staged with (18)f-fdg-pet-ct
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7334798/
https://www.ncbi.nlm.nih.gov/pubmed/32642564
http://dx.doi.org/10.1016/j.ctro.2020.06.008
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