Hamza Chegraoui
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Research Interests
Hamza Chegraoui has a total of 8 co-authors. Here are the top co-authors by number of shared publications:
- Antoine Grigis
Université Paris-Saclay, CEA, CNRS, BAOBAB
1 shared publication - Cathy Philippe
UNATI, Neurospin, Institut Joliot, CEA, Universite Paris-Saclay, Gif-sur-Yvette 91191, France
1 shared publication - Frédérique Frouin
Inserm/CEA/Université Paris Sud/CNRS, CEA/I2BM/SHFJ, Laboratoire IMIV, Orsay, France
1 shared publication - Jacques Grill
Gustave Roussy, Villejuif, France
1 shared publication - Nathalie Boddaert
Université Paris Cité, Inserm, Institut Imagine, Paris, France (P.C., V.D.-R., N.B., C.-J.R.).
1 shared publication - Raphael Calmon
Pediatric Radiology Department, Hôpital Necker Enfants Malades, APHP, IMAGINE Institute, Inserm, Université de Paris, 75015 Paris, France
1 shared publication
Latest Publications
- Open Access
Object Detection Improves Tumour Segmentation in MR Images of Rare Brain Tumours
Tumour lesion segmentation is a key step to study and characterise cancer from MR neuroradiological images. Presently, numerous deep learning segmentation architectures have been shown to perform well on the specific tumour type they are trained on (e.g., glioblastoma in brain hemispheres). However, a high performing network heavily trained on a given tumour type may perform poorly on a rare tumour type for which no labelled cases allows training or transfer learning. Yet, because some visual similarities exist nevertheless between common and rare tumours, in the lesion and around it, one may split the problem into two steps: object detection and segmentation. For each step, trained networks on common lesions could be used on rare ones following a domain adaptation scheme without extra fine-tuning. This work proposes a resilient tumour lesion delineation strategy, based on the combination of established elementary networks that achieve detection and segmentation. Our strategy allowed us to achieve robust segmentation inference on a rare tumour located in an unseen tumour context region during training. As an example of a rare tumour, Diffuse Intrinsic Pontine Glioma (DIPG), we achieve an average dice score of 0.62 without further training or network architecture adaptation.
Open AccessObject Detection Improves Tumour Segmentation in MR Images of Rare Brain Tumours
Tumour lesion segmentation is a key step to study and characterise cancer from MR neuroradiological images. Presently, numerous deep learning segmentation architectures have been shown to perform well on the specific tumour type they are trained on (e.g., glioblastoma in brain hemispheres). However, a high performing network heavily trained on a given tumour type may perform poorly on a rare tumour type for which no labelled cases allows training or transfer learning. Yet, because some visual similarities exist nevertheless between common and rare tumours, in the lesion and around it, one may split the problem into two steps: object detection and segmentation. For each step, trained networks on common lesions could be used on rare ones following a domain adaptation scheme without extra fine-tuning. This work proposes a resilient tumour lesion delineation strategy, based on the combination of established elementary networks that achieve detection and segmentation. Our strategy allowed us to achieve robust segmentation inference on a rare tumour located in an unseen tumour context region during training. As an example of a rare tumour, Diffuse Intrinsic Pontine Glioma (DIPG), we achieve an average dice score of 0.62 without further training or network architecture adaptation.