Cancers (Jun 2020)

Prognostic Impact of Pretherapeutic FDG-PET in Localized Anal Cancer

  • Maelle Le Thiec,
  • Aude Testard,
  • Ludovic Ferrer,
  • Camille Guillerminet,
  • Olivier Morel,
  • Bruno Maucherat,
  • Daniela Rusu,
  • Sylvie Girault,
  • Marie Lacombe,
  • Hadji Hamidou,
  • Véronique Guérin Meyer,
  • Emmanuel Rio,
  • Sandrine Hiret,
  • Françoise Kraeber-Bodéré,
  • Loïc Campion,
  • Caroline Rousseau

DOI
https://doi.org/10.3390/cancers12061512
Journal volume & issue
Vol. 12, no. 6
p. 1512

Abstract

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Due to the heterogeneity of tumour mass segmentation methods and lack of consensus, our study evaluated the prognostic value of pretherapeutic positron emission tomography with fluorodeoxyglucose (FDG-PET) metabolic parameters using different segmentation methods in patients with localized anal squamous cell carcinoma (SCC). Eighty-one patients with FDG-PET before radiochemotherapy were retrospectively analyzed. Semiquantitative data were measured with three fixed thresholds (35%, 41% and 50% of Maximum Standardized Uptake Value (SUVmax)) and four segmentation methods based on iterative approaches (Black, Adaptive, Nestle and Fitting). Metabolic volumes of primary anal tumour (P-MTV) and total tumour load (T-MTV: P-MTV+ lymph node MTV) were calculated. The primary endpoint was event-free survival (EFS). Seven multivariate models were created to compare FDG-PET tumour volumes prognostic impact. For all segmentation thresholds, PET metabolic volume parameters were independent prognostic factor and T-MTV variable was consistently better associated with EFS than P-MTV. Patient’s sex was an independent variable and significantly correlated with EFS. With fixed threshold segmentation methods, 35% of SUVmax threshold seemed better correlated with EFS and the best cut-off for discrimination between a low and high risk of event occurrence was 40 cm3. Determination of T-MTV by FDG-PET using fixed threshold segmentation is useful for predicting EFS for primary anal SCC. If these data are confirmed in larger studies, FDG-PET could contribute to individualized patient therapies.

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