4.7 Article

Performance of an integrated multimodality image guidance and dose-planning system supporting tumor-targeted HDR brachytherapy for prostate cancer

Journal

RADIOTHERAPY AND ONCOLOGY
Volume 166, Issue -, Pages 154-161

Publisher

ELSEVIER IRELAND LTD
DOI: 10.1016/j.radonc.2021.11.026

Keywords

Prostate cancer; Brachytherapy; Image registration; Electromagnetic tracking; Navigation system

Funding

  1. Varian Medical systems and NSERC/CIHR
  2. Canada First Research Excellence Fund through the TransMedTech Institute

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This study reports on the accuracy and workflow performance of a prototype system in supporting tumor-targeted procedures. The system integrates multimodal image registration and electromagnetic tracking technologies, improving accuracy in navigation and targeting while allowing the use of partially visible catheters. However, image registration errors should be carefully considered.
Background and purpose: Advances in high-dose-rate brachytherapy to treat prostate cancer hinge on improved accuracy in navigation and targeting while optimizing a streamlined workflow. Multimodal image registration and electromagnetic (EM) tracking are two technologies integrated into a prototype system in the early phase of clinical evaluation. We aim to report on the system's accuracy and workflow performance in support of tumor-targeted procedures. Materials and methods: In a prospective study, we evaluated the system in 43 consecutive procedures after clinical deployment. We measured workflow efficiency and EM catheter reconstruction accuracy. We also evaluated the system's MRI-TRUS registration accuracy with/without deformation, and with/without y-axis rotation for urethral alignment at initialization. Results: The cohort included 32 focal brachytherapy and 11 integrated boost whole-gland implants. Mean procedure time excluding dose delivery was 38 min (range: 21-83) for focal, and 56 min (range: 38-89) for whole-gland implants; stable over time. EM catheter reconstructions achieved a mean difference between computed and measured free-length of 0.8 mm (SD 0.8, no corrections performed), and mean axial manual corrections 1.3 mm (SD 0.7). EM also enabled the clinical use of a non or partially visible catheter in 21% of procedures. Registration accuracy improved with y-axis rotation for urethral alignment at initialization and with the elastic registration (mTRE 3.42 mm, SD 1.49). Conclusion: The system supported tumor-targeting and was implemented with no demonstrable learning curve. EM reconstruction errors were small, correctable, and improved with calibration and control of external distortion sources; increasing confidence in the use of partially visible catheters. Image registration errors remained despite rotational alignment and deformation, and should be carefully considered. (C) 2021 Elsevier B.V. All rights reserved.

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