Fully automatic segmentation of diffuse large B cell lymphoma lesions on 3D FDG-PET/CT for total metabolic tumour volume prediction using a convolutional neural network.

Purpose: Lymphoma lesion detection and segmentation on whole-body FDG-PET/CT are a challenging task because of the diversity of involved nodes, organs or physiological uptakes. We sought to investigate the performances of a three-dimensional (3D) convolutional neural network (CNN) to automatically s...

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Publicado en:European Journal of Nuclear Medicine & Molecular Imaging Vol. 48; no. 5; pp. 1362 - 1371
Autores principales: Blanc-Durand, Paul, Jégou, Simon, Kanoun, Salim, Berriolo-Riedinger, Alina, Bodet-Milin, Caroline, Kraeber-Bodéré, Françoise, Carlier, Thomas, Le Gouill, Steven, Casasnovas, René-Olivier, Meignan, Michel, Itti, Emmanuel
Formato: Journal Article
Publicado: Springer Nature May2021
Acceso en línea:Ver este registro en EBSCOhost
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      dt: May2021
      vid: 48
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      pub: Springer Nature
      place: New York, New York
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        146692175
        10.1007/s00259-020-05080-7
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        atl: Fully automatic segmentation of diffuse large B cell lymphoma lesions on 3D FDG-PET/CT for total metabolic tumour volume prediction using a convolutional neural network.
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        au:
          Blanc-Durand, Paul
          Jégou, Simon
          Kanoun, Salim
          Berriolo-Riedinger, Alina
          Bodet-Milin, Caroline
          Kraeber-Bodéré, Françoise
          Carlier, Thomas
          Le Gouill, Steven
          Casasnovas, René-Olivier
          Meignan, Michel
          Itti, Emmanuel
        affil: Department of Nuclear Medicine, CHU H. Mondor, AP-HP, F-94010, Créteil, France
      sug:
      ab: Purpose: Lymphoma lesion detection and segmentation on whole-body FDG-PET/CT are a challenging task because of the diversity of involved nodes, organs or physiological uptakes. We sought to investigate the performances of a three-dimensional (3D) convolutional neural network (CNN) to automatically segment total metabolic tumour volume (TMTV) in large datasets of patients with diffuse large B cell lymphoma (DLBCL). Methods: The dataset contained pre-therapy FDG-PET/CT from 733 DLBCL patients of 2 prospective LYmphoma Study Association (LYSA) trials. The first cohort (n = 639) was used for training using a 5-fold cross validation scheme. The second cohort (n = 94) was used for external validation of TMTV predictions. Ground truth masks were manually obtained after a 41% SUVmax adaptive thresholding of lymphoma lesions. A 3D U-net architecture with 2 input channels for PET and CT was trained on patches randomly sampled within PET/CTs with a summed cross entropy and Dice similarity coefficient (DSC) loss. Segmentation performance was assessed by the DSC and Jaccard coefficients. Finally, TMTV predictions were validated on the second independent cohort. Results: Mean DSC and Jaccard coefficients (± standard deviation) in the validations set were 0.73 ± 0.20 and 0.68 ± 0.21, respectively. An underestimation of mean TMTV by − 12 mL (2.8%) ± 263 was found in the validation sets of the first cohort (P = 0.27). In the second cohort, an underestimation of mean TMTV by − 116 mL (20.8%) ± 425 was statistically significant (P = 0.01). Conclusion: Our CNN is a promising tool for automatic detection and segmentation of lymphoma lesions, despite slight underestimation of TMTV. The fully automatic and open-source features of this CNN will allow to increase both dissemination in routine practice and reproducibility of TMTV assessment in lymphoma patients.
      pubtype: Academic Journal
      doctype: Journal Article
      ougenre: Article
    language: English
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