Radiomics modelling in rectal cancer to predict disease-free survival: evaluation of different approaches.


Journal

The British journal of surgery
ISSN: 1365-2168
Titre abrégé: Br J Surg
Pays: England
ID NLM: 0372553

Informations de publication

Date de publication:
23 10 2021
Historique:
received: 16 11 2020
accepted: 11 04 2021
pubmed: 24 8 2021
medline: 15 12 2021
entrez: 23 8 2021
Statut: ppublish

Résumé

Radiomics may be useful in rectal cancer management. The aim of this study was to assess and compare different radiomics approaches over qualitative evaluation to predict disease-free survival (DFS) in patients with locally advanced rectal cancer treated with neoadjuvant therapy. Patients from a phase II, multicentre, randomized study (GRECCAR4; NCT01333709) were included retrospectively as a training set. An independent cohort of patients comprised the independent test set. For both time points and both sets, radiomic features were extracted from two-dimensional manual segmentation (MS), three-dimensional (3D) MS, and from bounding boxes. Radiomics predictive models of DFS were built using a hyperparameters-tuned random forests classifier. Additionally, radiomics models were compared with qualitative parameters, including sphincter invasion, extramural vascular invasion as determined by MRI (mrEMVI) at baseline, and tumour regression grade evaluated by MRI (mrTRG) after chemoradiotherapy (CRT). In the training cohort of 98 patients, all three models showed good performance with mean(s.d.) area under the curve (AUC) values ranging from 0.77(0.09) to 0.89(0.09) for prediction of DFS. The 3D radiomics model outperformed qualitative analysis based on mrEMVI and sphincter invasion at baseline (P = 0.038 and P = 0.027 respectively), and mrTRG after CRT (P = 0.017). In the independent test cohort of 48 patients, at baseline and after CRT the AUC ranged from 0.67(0.09) to 0.76(0.06). All three models showed no difference compared with qualitative analysis in the independent set. Radiomics models can predict DFS in patients with locally advanced rectal cancer.

Sections du résumé

BACKGROUND
Radiomics may be useful in rectal cancer management. The aim of this study was to assess and compare different radiomics approaches over qualitative evaluation to predict disease-free survival (DFS) in patients with locally advanced rectal cancer treated with neoadjuvant therapy.
METHODS
Patients from a phase II, multicentre, randomized study (GRECCAR4; NCT01333709) were included retrospectively as a training set. An independent cohort of patients comprised the independent test set. For both time points and both sets, radiomic features were extracted from two-dimensional manual segmentation (MS), three-dimensional (3D) MS, and from bounding boxes. Radiomics predictive models of DFS were built using a hyperparameters-tuned random forests classifier. Additionally, radiomics models were compared with qualitative parameters, including sphincter invasion, extramural vascular invasion as determined by MRI (mrEMVI) at baseline, and tumour regression grade evaluated by MRI (mrTRG) after chemoradiotherapy (CRT).
RESULTS
In the training cohort of 98 patients, all three models showed good performance with mean(s.d.) area under the curve (AUC) values ranging from 0.77(0.09) to 0.89(0.09) for prediction of DFS. The 3D radiomics model outperformed qualitative analysis based on mrEMVI and sphincter invasion at baseline (P = 0.038 and P = 0.027 respectively), and mrTRG after CRT (P = 0.017). In the independent test cohort of 48 patients, at baseline and after CRT the AUC ranged from 0.67(0.09) to 0.76(0.06). All three models showed no difference compared with qualitative analysis in the independent set.
CONCLUSION
Radiomics models can predict DFS in patients with locally advanced rectal cancer.

Identifiants

pubmed: 34423347
pii: 6356254
doi: 10.1093/bjs/znab191
doi:

Types de publication

Clinical Trial, Phase II Journal Article Multicenter Study Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1243-1250

Investigateurs

E Rullier (E)
B Lelong (B)
P Maingon (P)
J-J Tuech (JJ)
D Pezet (D)
M Rivoire (M)
B Meunier (B)
J Loriau (J)
A Valverde (A)
J-M Fabre (JM)
M Prudhomme (M)
E Cotte (E)
G Portier (G)
L Quero (L)
B Gallix (B)
C Lemanski (C)
M Ychou (M)
F Bibeau (F)

Informations de copyright

© The Author(s) 2021. Published by Oxford University Press on behalf of BJS Society Ltd. All rights reserved. For permissions, please email: journals.permissions@oup.com.

Auteurs

H Tibermacine (H)

Radiology Department, Institut du Cancer de Montpellier, University of Montpellier, Montpellier, France.
Institut de Recherche en Cancérologie de Montpellier, INSERM, U1194, Montpellier, France.

P Rouanet (P)

Surgical Oncology Department, Institut du Cancer de Montpellier, University of Montpellier, Montpellier, France.

M Sbarra (M)

Departmental Faculty of Medicine and Surgery, Unit of Diagnostic Imaging and Interventional Radiology, Università Campus Bio-Medico di Roma, 00128 Rome, Italy.

R Forghani (R)

Augmented Intelligence and Precision Health Laboratory (AIPHL), Department of Radiology and the Research Institute of the McGill University Health Centre, Montreal, Quebec, Canada.

C Reinhold (C)

Augmented Intelligence and Precision Health Laboratory (AIPHL), Department of Radiology and the Research Institute of the McGill University Health Centre, Montreal, Quebec, Canada.

S Nougaret (S)

Radiology Department, Institut du Cancer de Montpellier, University of Montpellier, Montpellier, France.
Institut de Recherche en Cancérologie de Montpellier, INSERM, U1194, Montpellier, France.

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