Branch duct-intraductal papillary mucinous neoplasms (BD-IPMNs): an MRI-based radiomic model to determine the malignant degeneration potential.


Journal

La Radiologia medica
ISSN: 1826-6983
Titre abrégé: Radiol Med
Pays: Italy
ID NLM: 0177625

Informations de publication

Date de publication:
Apr 2023
Historique:
received: 06 01 2023
accepted: 05 02 2023
medline: 24 4 2023
pubmed: 25 2 2023
entrez: 24 2 2023
Statut: ppublish

Résumé

Branch duct-intraductal papillary mucinous neoplasms (BD-IPMNs) are the most common pancreatic cystic tumors and have a low risk of malignant transformation. Features able to early identify high-risk BD-IPMNs are lacking, and guidelines currently rely on the occurrence of worrisome features (WF) and high-risk stigmata (HRS). In our study, we aimed to use a magnetic resonance imaging (MRI) radiomic model to identify features linked to a higher risk of malignant degeneration, and whether these appear before the occurrence of WF and HRS. We retrospectively evaluated adult patients with a known BD-IPMN who had had at least two contrast-enhanced MRI studies at our center and a 24-month minimum follow-up time. MRI acquisition protocol for the two examinations included pre- and post-contrast phases and diffusion-weighted imaging (DWI)/apparent diffusion coefficient (ADC) map. Patients were divided into two groups according to the development of WF or HRS at the end of the follow-up (Group 0 = no WF or HRS; Group 1 = WF or HRS). We segmented the MRI images and quantitative features were extracted and compared between the two groups. Features that showed significant differences (SF) were then included in a LASSO regression method to build a radiomic-based predictive model. We included 50 patients: 31 in Group 0 and 19 in Group 1. No patients in this cohort developed HRS. At baseline, 47, 67, 38, and 68 SF were identified for pre-contrast T1-weighted (T1-W) sequence, post-contrast T1-W sequence, T2-weighted (T2- W) sequence, and ADC map, respectively. At the end of follow-up, we found 69, 78, 53, and 91 SF, respectively. The radiomic-based predictive model identified 16 SF: more particularly, 5 SF for pre-contrast T1-W sequence, 6 for post-contrast T1-W sequence, 3 for T2-W sequence, and 2 for ADC. We identified radiomic features that correlate significantly with WF in patients with BD-IPMNs undergoing contrast-enhanced MRI. Our MRI-based radiomic model can predict the occurrence of WF.

Sections du résumé

BACKGROUND BACKGROUND
Branch duct-intraductal papillary mucinous neoplasms (BD-IPMNs) are the most common pancreatic cystic tumors and have a low risk of malignant transformation. Features able to early identify high-risk BD-IPMNs are lacking, and guidelines currently rely on the occurrence of worrisome features (WF) and high-risk stigmata (HRS).
AIM OBJECTIVE
In our study, we aimed to use a magnetic resonance imaging (MRI) radiomic model to identify features linked to a higher risk of malignant degeneration, and whether these appear before the occurrence of WF and HRS.
METHODS METHODS
We retrospectively evaluated adult patients with a known BD-IPMN who had had at least two contrast-enhanced MRI studies at our center and a 24-month minimum follow-up time. MRI acquisition protocol for the two examinations included pre- and post-contrast phases and diffusion-weighted imaging (DWI)/apparent diffusion coefficient (ADC) map. Patients were divided into two groups according to the development of WF or HRS at the end of the follow-up (Group 0 = no WF or HRS; Group 1 = WF or HRS). We segmented the MRI images and quantitative features were extracted and compared between the two groups. Features that showed significant differences (SF) were then included in a LASSO regression method to build a radiomic-based predictive model.
RESULTS RESULTS
We included 50 patients: 31 in Group 0 and 19 in Group 1. No patients in this cohort developed HRS. At baseline, 47, 67, 38, and 68 SF were identified for pre-contrast T1-weighted (T1-W) sequence, post-contrast T1-W sequence, T2-weighted (T2- W) sequence, and ADC map, respectively. At the end of follow-up, we found 69, 78, 53, and 91 SF, respectively. The radiomic-based predictive model identified 16 SF: more particularly, 5 SF for pre-contrast T1-W sequence, 6 for post-contrast T1-W sequence, 3 for T2-W sequence, and 2 for ADC.
CONCLUSION CONCLUSIONS
We identified radiomic features that correlate significantly with WF in patients with BD-IPMNs undergoing contrast-enhanced MRI. Our MRI-based radiomic model can predict the occurrence of WF.

Identifiants

pubmed: 36826452
doi: 10.1007/s11547-023-01609-6
pii: 10.1007/s11547-023-01609-6
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

383-392

Informations de copyright

© 2023. Italian Society of Medical Radiology.

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Auteurs

Federica Flammia (F)

Department of Radiology, Careggi University Hospital, Largo Brambilla 3, 50134, Florence, Italy.

Tommaso Innocenti (T)

Department of Experimental and Clinical Biomedical Sciences "Mario Serio", University of Florence, Viale G.B. Morgagni 50, 50134, Florence, Italy.
Clinical Gastroenterology Unit, Careggi University Hospital, Largo Brambilla 3, 50134, Florence, Italy.

Antonio Galluzzo (A)

Department of Radiology, Careggi University Hospital, Largo Brambilla 3, 50134, Florence, Italy.

Ginevra Danti (G)

Department of Radiology, Careggi University Hospital, Largo Brambilla 3, 50134, Florence, Italy. ginevra.danti@gmail.com.

Giuditta Chiti (G)

Department of Radiology, Careggi University Hospital, Largo Brambilla 3, 50134, Florence, Italy.

Giulia Grazzini (G)

Department of Radiology, Careggi University Hospital, Largo Brambilla 3, 50134, Florence, Italy.

Silvia Bettarini (S)

Department of Health Physics, Careggi University Hospital, Largo Brambilla 3, 50134, Florence, Italy.

Paolo Tortoli (P)

Department of Health Physics, Careggi University Hospital, Largo Brambilla 3, 50134, Florence, Italy.

Simone Busoni (S)

Department of Health Physics, Careggi University Hospital, Largo Brambilla 3, 50134, Florence, Italy.

Gabriele Dragoni (G)

Department of Experimental and Clinical Biomedical Sciences "Mario Serio", University of Florence, Viale G.B. Morgagni 50, 50134, Florence, Italy.
Clinical Gastroenterology Unit, Careggi University Hospital, Largo Brambilla 3, 50134, Florence, Italy.

Matteo Gottin (M)

Department of Experimental and Clinical Biomedical Sciences "Mario Serio", University of Florence, Viale G.B. Morgagni 50, 50134, Florence, Italy.
Clinical Gastroenterology Unit, Careggi University Hospital, Largo Brambilla 3, 50134, Florence, Italy.

Andrea Galli (A)

Department of Experimental and Clinical Biomedical Sciences "Mario Serio", University of Florence, Viale G.B. Morgagni 50, 50134, Florence, Italy.
Clinical Gastroenterology Unit, Careggi University Hospital, Largo Brambilla 3, 50134, Florence, Italy.

Vittorio Miele (V)

Department of Radiology, Careggi University Hospital, Largo Brambilla 3, 50134, Florence, Italy.

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