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


Journal

Radiation oncology (London, England)
ISSN: 1748-717X
Titre abrégé: Radiat Oncol
Pays: England
ID NLM: 101265111

Informations de publication

Date de publication:
06 Aug 2019
Historique:
received: 15 05 2019
accepted: 18 07 2019
entrez: 8 8 2019
pubmed: 8 8 2019
medline: 8 2 2020
Statut: epublish

Résumé

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). 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. 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). FDG-PET parameters are predictive of recurrence in AC. FDG-PET may represent a valuable tool for prognostication and response assessment in AC. ANZCTR, ACTRN12614001219673 . Registered 19 November 2014 - Retrospectively registered.

Sections du résumé

BACKGROUND 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 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 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 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 BACKGROUND
ANZCTR, ACTRN12614001219673 . Registered 19 November 2014 - Retrospectively registered.

Identifiants

pubmed: 31387597
doi: 10.1186/s13014-019-1342-9
pii: 10.1186/s13014-019-1342-9
pmc: PMC6685144
doi:

Substances chimiques

Radiopharmaceuticals 0
Fluorodeoxyglucose F18 0Z5B2CJX4D

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

140

Subventions

Organisme : The Royal Australian and New Zealand College of Radiologists
ID : 2014/RANZCR/006
Organisme : Hunter Translational Cancer Research Grant
ID : NA

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Auteurs

Michael Peter Jones (MP)

WP Holman Clinic, Royal Hobart Hospital, Hobart, Tasmania, Australia. Michael.Jones@ths.tas.gov.au.
The University of Newcastle, Callaghan, New South Wales, Australia. Michael.Jones@ths.tas.gov.au.

George Hruby (G)

Department of Radiation Oncology, Royal North Shore Hospital, St Leonards, New South Wales, Australia.

Ur Metser (U)

Department of Medical Imaging, Princess Margaret Cancer Centre, Toronto, Ontario, Canada.

Swetha Sridharan (S)

Department of Radiation Oncology, Calvary Mater Newcastle, Waratah, New South Wales, Australia.

Anne Capp (A)

Department of Radiation Oncology, Calvary Mater Newcastle, Waratah, New South Wales, Australia.

Mahesh Kumar (M)

Department of Radiation Oncology, Calvary Mater Newcastle, Waratah, New South Wales, Australia.

Sarah Gallagher (S)

Department of Radiation Oncology, Calvary Mater Newcastle, Waratah, New South Wales, Australia.

Natalie Rutherford (N)

Department of Nuclear Medicine, Calvary Mater Newcastle, Waratah, New South Wales, Australia.

Carl Holder (C)

Hunter Medical Research Institute, New Lambton Heights, New South Wales, Australia.

Christopher Oldmeadow (C)

Hunter Medical Research Institute, New Lambton Heights, New South Wales, Australia.

Jarad Martin (J)

The University of Newcastle, Callaghan, New South Wales, Australia.
Department of Radiation Oncology, Calvary Mater Newcastle, Waratah, New South Wales, Australia.

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Classifications MeSH