Proton range uncertainty caused by synthetic computed tomography generated with deep learning from pelvic magnetic resonance imaging.


Journal

Acta oncologica (Stockholm, Sweden)
ISSN: 1651-226X
Titre abrégé: Acta Oncol
Pays: England
ID NLM: 8709065

Informations de publication

Date de publication:
Nov 2023
Historique:
medline: 8 11 2023
pubmed: 13 9 2023
entrez: 13 9 2023
Statut: ppublish

Résumé

In proton therapy, it is disputed whether synthetic computed tomography (sCT), derived from magnetic resonance imaging (MRI), permits accurate dose calculations. On the one hand, an MRI-only workflow could eliminate errors caused by, e.g., MRI-CT registration. On the other hand, the extra error would be induced due to an sCT generation model. This work investigated the systematic and random model error induced by sCT generation of a widely discussed deep learning model, pix2pix. An open-source image dataset of 19 patients with cancer in the pelvis was employed and split into 10, 5, and 4 for training, testing, and validation of the model, respectively. Proton pencil beams (200 MeV) were simulated on the real CT and generated sCT using the tool for particle simulation (TOPAS). Monte Carlo (MC) dropout was used for error estimation (50 random sCT samples). Systematic and random model errors were investigated for sCT generation and dose calculation on sCT. For sCT generation, random model error near the edge of the body (∼200 HU) was higher than that within the body (∼100 HU near the bone edge and <10 HU in soft tissue). The mean absolute error (MAE) was 49 ± 5, 191 ± 23, and 503 ± 70 HU for the whole body, bone, and air in the patient, respectively. Random model errors of the proton range were small (<0.2 mm) for all spots and evenly distributed throughout the proton fields. Systematic errors of the proton range were -1.0(±2.2) mm and 0.4(±0.9)%, respectively, and were unevenly distributed within the proton fields. For 4.5% of the spots, large errors (>5 mm) were found, which may relate to MRI-CT mismatch due to, e.g., registration, MRI distortion anatomical changes, etc. The sCT model was shown to be robust, i.e., had a low random model error. However, further investigation to reduce and even predict and manage systematic error is still needed for future MRI-only proton therapy.

Sections du résumé

BACKGROUND UNASSIGNED
In proton therapy, it is disputed whether synthetic computed tomography (sCT), derived from magnetic resonance imaging (MRI), permits accurate dose calculations. On the one hand, an MRI-only workflow could eliminate errors caused by, e.g., MRI-CT registration. On the other hand, the extra error would be induced due to an sCT generation model. This work investigated the systematic and random model error induced by sCT generation of a widely discussed deep learning model, pix2pix.
MATERIAL AND METHODS UNASSIGNED
An open-source image dataset of 19 patients with cancer in the pelvis was employed and split into 10, 5, and 4 for training, testing, and validation of the model, respectively. Proton pencil beams (200 MeV) were simulated on the real CT and generated sCT using the tool for particle simulation (TOPAS). Monte Carlo (MC) dropout was used for error estimation (50 random sCT samples). Systematic and random model errors were investigated for sCT generation and dose calculation on sCT.
RESULTS UNASSIGNED
For sCT generation, random model error near the edge of the body (∼200 HU) was higher than that within the body (∼100 HU near the bone edge and <10 HU in soft tissue). The mean absolute error (MAE) was 49 ± 5, 191 ± 23, and 503 ± 70 HU for the whole body, bone, and air in the patient, respectively. Random model errors of the proton range were small (<0.2 mm) for all spots and evenly distributed throughout the proton fields. Systematic errors of the proton range were -1.0(±2.2) mm and 0.4(±0.9)%, respectively, and were unevenly distributed within the proton fields. For 4.5% of the spots, large errors (>5 mm) were found, which may relate to MRI-CT mismatch due to, e.g., registration, MRI distortion anatomical changes, etc.
CONCLUSION UNASSIGNED
The sCT model was shown to be robust, i.e., had a low random model error. However, further investigation to reduce and even predict and manage systematic error is still needed for future MRI-only proton therapy.

Identifiants

pubmed: 37703314
doi: 10.1080/0284186X.2023.2256967
doi:

Substances chimiques

Protons 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1461-1469

Auteurs

Liheng Tian (L)

Department of Physics, TU Dortmund University, Dortmund, Germany.

Armin Lühr (A)

Department of Physics, TU Dortmund University, Dortmund, Germany.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH