Incremental retraining, clinical implementation, and acceptance rate of deep learning auto-segmentation for male pelvis in a multiuser environment.


Journal

Medical physics
ISSN: 2473-4209
Titre abrégé: Med Phys
Pays: United States
ID NLM: 0425746

Informations de publication

Date de publication:
Jul 2023
Historique:
revised: 02 05 2023
received: 07 03 2023
accepted: 23 05 2023
medline: 11 7 2023
pubmed: 8 6 2023
entrez: 8 6 2023
Statut: ppublish

Résumé

Deep learning auto-segmentation (DLAS) models have been adopted in the clinic; however, they suffer from performance deterioration owing to the clinical practice variability. Some commercial DLAS software provide an incremental retraining function that enables users to train a custom model using their institutional data to account for clinical practice variability. This study was performed to evaluate and implement the commercial DLAS software with the incremental retraining function for definitive treatment of patients with prostate cancer in a multi-user environment. CT-based target organs and organs-at-risk (OAR) delineation of 215 prostate cancer patients were utilized. The performance of three commercial DLAS software built-in models was validated with 20 patients. A retrained custom model was developed using 100 patients and evaluated on the remaining data (n = 115). Dice similarity coefficient (DSC), Hausdorff distance (HD), mean surface distance (MSD), and surface DSC (SDSC) were utilized for quantitative evaluation. A multi-rater qualitative evaluation was blindly performed with a five-level scale. Visual inspection was performed in consensus and non-consensus unacceptable cases to identify the failure modes. Three commercial DLAS vendor built-in models achieved sub-optimal performance in 20 patients. The retrained custom model had a mean DSC of 0.82 for prostate, 0.48 for seminal vesicles (SV), and 0.92 for rectum, respectively. This represents a significant improvement over the built-in model with DSC of 0.73, 0.37, and 0.81 for the corresponding structures. Compared to the acceptance rate of 96.5% and consensus unacceptable rate (i.e., both reviewers rated as unacceptable) of 3.5% achieved by manual contours, the custom model achieved a 91.3% acceptance rate and 8.7% consensus unacceptable rate. The failure modes of retrained custom model were attributed to the following: cystogram (n = 2), hip prosthesis (n = 2), low dose rate brachytherapy seeds (n = 2), air in endorectal balloon(n = 1), non-iodinated spacer (n = 2), and giant bladder(n = 1). The commercial DLAS software with the incremental retraining function was validated and clinically adopted for prostate patients in a multi-user environment. AI-based auto-delineation of the prostate and OARs is shown to achieve improved physician acceptance, overall clinical utility, and accuracy.

Sections du résumé

BACKGROUND BACKGROUND
Deep learning auto-segmentation (DLAS) models have been adopted in the clinic; however, they suffer from performance deterioration owing to the clinical practice variability. Some commercial DLAS software provide an incremental retraining function that enables users to train a custom model using their institutional data to account for clinical practice variability.
PURPOSE OBJECTIVE
This study was performed to evaluate and implement the commercial DLAS software with the incremental retraining function for definitive treatment of patients with prostate cancer in a multi-user environment.
METHODS METHODS
CT-based target organs and organs-at-risk (OAR) delineation of 215 prostate cancer patients were utilized. The performance of three commercial DLAS software built-in models was validated with 20 patients. A retrained custom model was developed using 100 patients and evaluated on the remaining data (n = 115). Dice similarity coefficient (DSC), Hausdorff distance (HD), mean surface distance (MSD), and surface DSC (SDSC) were utilized for quantitative evaluation. A multi-rater qualitative evaluation was blindly performed with a five-level scale. Visual inspection was performed in consensus and non-consensus unacceptable cases to identify the failure modes.
RESULTS RESULTS
Three commercial DLAS vendor built-in models achieved sub-optimal performance in 20 patients. The retrained custom model had a mean DSC of 0.82 for prostate, 0.48 for seminal vesicles (SV), and 0.92 for rectum, respectively. This represents a significant improvement over the built-in model with DSC of 0.73, 0.37, and 0.81 for the corresponding structures. Compared to the acceptance rate of 96.5% and consensus unacceptable rate (i.e., both reviewers rated as unacceptable) of 3.5% achieved by manual contours, the custom model achieved a 91.3% acceptance rate and 8.7% consensus unacceptable rate. The failure modes of retrained custom model were attributed to the following: cystogram (n = 2), hip prosthesis (n = 2), low dose rate brachytherapy seeds (n = 2), air in endorectal balloon(n = 1), non-iodinated spacer (n = 2), and giant bladder(n = 1).
CONCLUSION CONCLUSIONS
The commercial DLAS software with the incremental retraining function was validated and clinically adopted for prostate patients in a multi-user environment. AI-based auto-delineation of the prostate and OARs is shown to achieve improved physician acceptance, overall clinical utility, and accuracy.

Identifiants

pubmed: 37287322
doi: 10.1002/mp.16537
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

4079-4091

Subventions

Organisme : NCI NIH HHS
ID : 75N91020C00048
Pays : United States
Organisme : NCI NIH HHS
ID : 75N91020C00048
Pays : United States

Informations de copyright

© 2023 American Association of Physicists in Medicine.

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Auteurs

Jingwei Duan (J)

Department of Radiation Oncology, Mayo Clinic Arizona, Phoenix, Arizona, USA.
Department of Radiation Oncology, University of Kentucky, Lexington, Kentucky, USA.

Carlos E Vargas (CE)

Department of Radiation Oncology, Mayo Clinic Arizona, Phoenix, Arizona, USA.

Nathan Y Yu (NY)

Department of Radiation Oncology, Mayo Clinic Arizona, Phoenix, Arizona, USA.

Brady S Laughlin (BS)

Department of Radiation Oncology, Mayo Clinic Arizona, Phoenix, Arizona, USA.

Diego Santos Toesca (DS)

Department of Radiation Oncology, Mayo Clinic Arizona, Phoenix, Arizona, USA.

Sameer Keole (S)

Department of Radiation Oncology, Mayo Clinic Arizona, Phoenix, Arizona, USA.

Jean Claude M Rwigema (JCM)

Department of Radiation Oncology, Mayo Clinic Arizona, Phoenix, Arizona, USA.

William W Wong (WW)

Department of Radiation Oncology, Mayo Clinic Arizona, Phoenix, Arizona, USA.

Steven E Schild (SE)

Department of Radiation Oncology, Mayo Clinic Arizona, Phoenix, Arizona, USA.

Xue Feng (X)

Carina Medical LLC, Lexington, Kentucky, USA.

Quan Chen (Q)

Department of Radiation Oncology, City of Hope Comprehensive Cancer Center, Duarte, California, USA.

Yi Rong (Y)

Department of Radiation Oncology, Mayo Clinic Arizona, Phoenix, Arizona, USA.

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