Deep-Learning F-FDG Uptake Classification Enables Total Metabolic Tumor Volume Estimation in Diffuse Large B-Cell Lymphoma.

Journal: Journal of nuclear medicine : official publication, Society of Nuclear Medicine
PMID:

Abstract

Total metabolic tumor volume (TMTV), calculated from F-FDG PET/CT baseline studies, is a prognostic factor in diffuse large B-cell lymphoma (DLBCL) whose measurement requires the segmentation of all malignant foci throughout the body. No consensus currently exists regarding the most accurate approach for such segmentation. Further, all methods still require extensive manual input from an experienced reader. We examined whether an artificial intelligence-based method could estimate TMTV with a comparable prognostic value to TMTV measured by experts. Baseline F-FDG PET/CT scans of 301 DLBCL patients from the REMARC trial (NCT01122472) were retrospectively analyzed using a prototype software (PET Assisted Reporting System [PARS]). An automated whole-body high-uptake segmentation algorithm identified all 3-dimensional regions of interest (ROIs) with increased tracer uptake. The resulting ROIs were processed using a convolutional neural network trained on an independent cohort and classified as nonsuspicious or suspicious uptake. The PARS-based TMTV (TMTV) was estimated as the sum of the volumes of ROIs classified as suspicious uptake. The reference TMTV (TMTV) was measured by 2 experienced readers using independent semiautomatic software. The TMTV was compared with the TMTV in terms of prognostic value for progression-free survival (PFS) and overall survival (OS). TMTV was significantly correlated with the TMTV (ρ = 0.76; < 0.001). Using PARS, an average of 24 regions per subject with increased tracer uptake was identified, and an average of 20 regions per subject was correctly identified as nonsuspicious or suspicious, yielding 85% classification accuracy, 80% sensitivity, and 88% specificity, compared with the TMTV region. Both TMTV results were predictive of PFS (hazard ratio, 2.3 and 2.6 for TMTV and TMTV, respectively; < 0.001) and OS (hazard ratio, 2.8 and 3.7 for TMTV and TMTV, respectively; < 0.001). TMTV was consistent with that obtained by experts and displayed a significant prognostic value for PFS and OS in DLBCL patients. Classification of high-uptake regions using deep learning for rapidly discarding physiologic uptake may considerably simplify TMTV estimation, reduce observer variability, and facilitate the use of TMTV as a predictive factor in DLBCL patients.

Authors

  • Nicolò Capobianco
    Siemens Healthcare GmbH, Erlangen, Germany nicolo.capobianco@siemens-healthineers.com.
  • Michel Meignan
    Lysa Imaging, Henri Mondor University Hospitals, APHP, University Paris East, Créteil, France.
  • Anne-Ségolène Cottereau
    Department of Nuclear Medicine, Cochin Hospital, AP-HP, Paris, France.
  • Laetitia Vercellino
    Department of Nuclear Medicine, Saint-Louis Hospital, AP-HP, Paris, France.
  • Ludovic Sibille
    Siemens Medical Solutions USA, Inc., Knoxville, Tennessee.
  • Bruce Spottiswoode
    Siemens Medical Solutions USA, Inc., Knoxville, Tennessee.
  • Sven Zuehlsdorff
    Siemens Medical Solutions USA, Inc., Knoxville, Tennessee.
  • Olivier Casasnovas
    Department of Hematology, University Hospital of Dijon, Dijon, France.
  • Catherine Thieblemont
    Department of Hematology, Saint Louis Hospital, APHP, Paris, France; and.
  • Irène Buvat
    Imagerie Moléculaire In Vivo, CEA, Inserm, Univ Paris Sud, CNRS, Université Paris Saclay, Orsay, France.