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FDG-PET parameters predict for recurrence in anal cancer – results from a prospective, multicentre clinical trial

BACKGROUND: To investigate the prognostic significance of positron emission tomography (PET) parameters from F-18 fluorodeoxyglucose (FDG) PET scans performed pre- and post- chemo-radiotherapy (CRT) for squamous cell carcinoma of the anal canal (AC). METHODS: From January 2013 to January 2017, 19 pa...

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Autores principales: Jones, Michael Peter, Hruby, George, Metser, Ur, Sridharan, Swetha, Capp, Anne, Kumar, Mahesh, Gallagher, Sarah, Rutherford, Natalie, Holder, Carl, Oldmeadow, Christopher, Martin, Jarad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6685144/
https://www.ncbi.nlm.nih.gov/pubmed/31387597
http://dx.doi.org/10.1186/s13014-019-1342-9
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author Jones, Michael Peter
Hruby, George
Metser, Ur
Sridharan, Swetha
Capp, Anne
Kumar, Mahesh
Gallagher, Sarah
Rutherford, Natalie
Holder, Carl
Oldmeadow, Christopher
Martin, Jarad
author_facet Jones, Michael Peter
Hruby, George
Metser, Ur
Sridharan, Swetha
Capp, Anne
Kumar, Mahesh
Gallagher, Sarah
Rutherford, Natalie
Holder, Carl
Oldmeadow, Christopher
Martin, Jarad
author_sort Jones, Michael Peter
collection PubMed
description BACKGROUND: To investigate the prognostic significance of positron emission tomography (PET) parameters from F-18 fluorodeoxyglucose (FDG) PET scans performed pre- and post- chemo-radiotherapy (CRT) for squamous cell carcinoma of the anal canal (AC). METHODS: From January 2013 to January 2017, 19 patients with non-metastatic AC enrolled on a prospective trial underwent FDG-PET/CT imaging before and 12 weeks following CRT. A computer-generated volume of interest (VOI) was snapped around the primary tumour using six different standard uptake value (SUV) thresholds and the following parameters were extracted: SUV max, mean, median, standard deviation and peak as well as metabolic tumour volume (MTV) and total lesion glycolysis. Exact logistic regression and ROC AUC analyses were performed for each metric at each timepoint. RESULTS: With a median follow up of 15.8 months, 3/19 patients had a local recurrence and 5/19 had any recurrence. On post-CRT PET, the median SUV within a VOI bounded by an SUV of 3 correlated with local recurrence (p < 0.01) and demonstrated excellent discrimination (ROC AUC 1.00, perfect separation was achieved at a median SUV of 3.38). The mean SUV at this threshold did not quite reach significance for prediction of local recurrence (p = 0.06) but demonstrated excellent discrimination (ROC AUC 0.91). The MTV bounded by a threshold of 41% SUVmax on the pre-CRT PET predicted for any recurrence (p = 0.03) and showed excellent discrimination (ROC AUC 0.89). CONCLUSIONS: FDG-PET parameters are predictive of recurrence in AC. FDG-PET may represent a valuable tool for prognostication and response assessment in AC. TRIAL REGISTRATION: ANZCTR, ACTRN12614001219673. Registered 19 November 2014 - Retrospectively registered.
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spelling pubmed-66851442019-08-12 FDG-PET parameters predict for recurrence in anal cancer – results from a prospective, multicentre clinical trial Jones, Michael Peter Hruby, George Metser, Ur Sridharan, Swetha Capp, Anne Kumar, Mahesh Gallagher, Sarah Rutherford, Natalie Holder, Carl Oldmeadow, Christopher Martin, Jarad Radiat Oncol Research BACKGROUND: To investigate the prognostic significance of positron emission tomography (PET) parameters from F-18 fluorodeoxyglucose (FDG) PET scans performed pre- and post- chemo-radiotherapy (CRT) for squamous cell carcinoma of the anal canal (AC). METHODS: From January 2013 to January 2017, 19 patients with non-metastatic AC enrolled on a prospective trial underwent FDG-PET/CT imaging before and 12 weeks following CRT. A computer-generated volume of interest (VOI) was snapped around the primary tumour using six different standard uptake value (SUV) thresholds and the following parameters were extracted: SUV max, mean, median, standard deviation and peak as well as metabolic tumour volume (MTV) and total lesion glycolysis. Exact logistic regression and ROC AUC analyses were performed for each metric at each timepoint. RESULTS: With a median follow up of 15.8 months, 3/19 patients had a local recurrence and 5/19 had any recurrence. On post-CRT PET, the median SUV within a VOI bounded by an SUV of 3 correlated with local recurrence (p < 0.01) and demonstrated excellent discrimination (ROC AUC 1.00, perfect separation was achieved at a median SUV of 3.38). The mean SUV at this threshold did not quite reach significance for prediction of local recurrence (p = 0.06) but demonstrated excellent discrimination (ROC AUC 0.91). The MTV bounded by a threshold of 41% SUVmax on the pre-CRT PET predicted for any recurrence (p = 0.03) and showed excellent discrimination (ROC AUC 0.89). CONCLUSIONS: FDG-PET parameters are predictive of recurrence in AC. FDG-PET may represent a valuable tool for prognostication and response assessment in AC. TRIAL REGISTRATION: ANZCTR, ACTRN12614001219673. Registered 19 November 2014 - Retrospectively registered. BioMed Central 2019-08-06 /pmc/articles/PMC6685144/ /pubmed/31387597 http://dx.doi.org/10.1186/s13014-019-1342-9 Text en © The Author(s). 2019 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. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Jones, Michael Peter
Hruby, George
Metser, Ur
Sridharan, Swetha
Capp, Anne
Kumar, Mahesh
Gallagher, Sarah
Rutherford, Natalie
Holder, Carl
Oldmeadow, Christopher
Martin, Jarad
FDG-PET parameters predict for recurrence in anal cancer – results from a prospective, multicentre clinical trial
title FDG-PET parameters predict for recurrence in anal cancer – results from a prospective, multicentre clinical trial
title_full FDG-PET parameters predict for recurrence in anal cancer – results from a prospective, multicentre clinical trial
title_fullStr FDG-PET parameters predict for recurrence in anal cancer – results from a prospective, multicentre clinical trial
title_full_unstemmed FDG-PET parameters predict for recurrence in anal cancer – results from a prospective, multicentre clinical trial
title_short FDG-PET parameters predict for recurrence in anal cancer – results from a prospective, multicentre clinical trial
title_sort fdg-pet parameters predict for recurrence in anal cancer – results from a prospective, multicentre clinical trial
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6685144/
https://www.ncbi.nlm.nih.gov/pubmed/31387597
http://dx.doi.org/10.1186/s13014-019-1342-9
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