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Effect of synthetic CT on dose-derived toxicity predictors for MR-only prostate radiotherapy.
Thomas, Christopher; Dregely, Isabel; Oksuz, Ilkay; Guerrero Urbano, Teresa; Greener, Tony; King, Andrew P; Barrington, Sally F.
Afiliação
  • Thomas C; School of Biomedical Engineering & Imaging Sciences, King's College London, SE17EH London, United Kingdom.
  • Dregely I; Medical Physics Department, Guy's and St Thomas' Hospital NHS Foundation Trust, SE17EH London, United Kingdom.
  • Oksuz I; School of Biomedical Engineering & Imaging Sciences, King's College London, SE17EH London, United Kingdom.
  • Guerrero Urbano T; Computer Science, UAS Technikum Wien, 1200 Vienna, Austria.
  • Greener T; School of Biomedical Engineering & Imaging Sciences, King's College London, SE17EH London, United Kingdom.
  • King AP; Computer Engineering Department, Istanbul Technical University, 34485 Istanbul, Turkey.
  • Barrington SF; Clinical Oncology, Guy's and St Thomas' Hospital NHS Foundation Trust, SE17EH London, United Kingdom.
BJR Open ; 6(1): tzae014, 2024 Jan.
Article em En | MEDLINE | ID: mdl-38948455
ABSTRACT

Objectives:

Toxicity-driven adaptive radiotherapy (RT) is enhanced by the superior soft tissue contrast of magnetic resonance (MR) imaging compared with conventional computed tomography (CT). However, in an MR-only RT pathway synthetic CTs (sCT) are required for dose calculation. This study evaluates 3 sCT approaches for accurate rectal toxicity prediction in prostate RT.

Methods:

Thirty-six patients had MR (T2-weighted acquisition optimized for anatomical delineation, and T1-Dixon) with same day standard-of-care planning CT for prostate RT. Multiple sCT were created per patient using bulk density (BD), tissue stratification (TS, from T1-Dixon) and deep-learning (DL) artificial intelligence (AI) (from T2-weighted) approaches for dose distribution calculation and creation of rectal dose volume histograms (DVH) and dose surface maps (DSM) to assess grade-2 (G2) rectal bleeding risk.

Results:

Maximum absolute errors using sCT for DVH-based G2 rectal bleeding risk (risk range 1.6% to 6.1%) were 0.6% (BD), 0.3% (TS) and 0.1% (DL). DSM-derived risk prediction errors followed a similar pattern. DL sCT has voxel-wise density generated from T2-weighted MR and improved accuracy for both risk-prediction methods.

Conclusions:

DL improves dosimetric and predicted risk calculation accuracy. Both TS and DL methods are clinically suitable for sCT generation in toxicity-guided RT, however, DL offers increased accuracy and offers efficiencies by removing the need for T1-Dixon MR. Advances in knowledge This study demonstrates novel insights regarding the effect of sCT on predictive toxicity metrics, demonstrating clear accuracy improvement with increased sCT resolution. Accuracy of toxicity calculation in MR-only RT should be assessed for all treatment sites where dose to critical structures will guide adaptive-RT strategies. Clinical trial registration number Patient data were taken from an ethically approved (UK Health Research Authority) clinical trial run at Guy's and St Thomas' NHS Foundation Trust. Study Name MR-simulation in Radiotherapy for Prostate Cancer. ClinicalTrials.gov Identifier NCT03238170.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article