Copenhagen, Denmark
Onsite/Online

ESTRO 2022

Session Item

Implementation of new technology and techniques
7002
Poster (digital)
Physics
Fully automated rigid image registration versus human registration in postoperative spine SBRT
Yutaro Koide, Japan
PO-1681

Abstract

Fully automated rigid image registration versus human registration in postoperative spine SBRT
Authors:

Yutaro Koide1, Hidetoshi Shimizu1, Risei Miyauchi1, Shouichi Haimoto2, Hiroshi Tanaka3, Yui Watanabe4, Sou Adachi5, Daiki Kato6, Takahiro Aoyama1, Tomoki Kitagawa1, Hiroyuki Tachibana1, Takeshi Kodaira1

1Aichi Cancer Center, Radiation Oncology, Nagoya, Japan; 2Aichi Cancer Center, Neurosurgery, Nagoya, Japan; 3Shiokawa Hospital Gamma Knife Center, Radiation Oncology, Suzuka, Japan; 4Yachiyo Hospital Radiation Therapy Center, Radiation Oncology, Anjo, Japan; 5Aichi Medical University Hospital, Radiology, Nagakute, Japan; 6Daiyukai General Hospital, Radiology, Ichinomiya, Japan

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Purpose or Objective

Spine stereotactic body radiation therapy (SBRT) planning requires accurate image registration of MRI/CT-myelogram to the planning CT for spinal cord delineation. To confirm the fully automated rigid image registration (A-RIR) accuracy in postoperative spine SBRT, we conducted a multicenter non-inferiority study compared to the human registration (H-RIR).

Material and Methods

Twenty-eight metastatic cancer patients who underwent postoperative spine SBRT are enrolled. All patients underwent planning CT scans in the immobilized supine position under the following conditions: field of view = 550 mm, slice thickness = 1 mm, the spatial resolution = 1.074 mm/pixel. CT-myelogram was obtained for spinal cord delineation through an intrathecal injection of iohexol contrast, followed by CT simulation. The adopted A-RIR workflow is a contour-focused algorithm performing a rigid registration by maximizing normalized mutual information (NMI) restricted to the data contained within the automatically extracted contour. The A-RIR and H-RIR were performed after an NMI-based RIR on the whole image as the baseline. Three radiation oncologists from multicenter were prompted to review two blinded registrations and choose one for clinical use. Indistinguishable cases were allowed to vote equivalent, counted A-RIR side. A-RIR is considered non-inferior to H-RIR if the lower limit of the 95% confidence interval (CI) of A-RIR preferable/equivalent is greater than 0.45. We also evaluated the NMI improvement from the baseline and the translational/rotational errors between A-RIR and H-RIR.

Results

The A-RIR preferable/equivalent was selected in twenty-one patients (0.75, 95% CI: 0.55–0.89), demonstrating non-inferiority to H-RIR. The NMI improvement of A-RIR was greater than that of H-RIR in twenty-four patients: the mean value ± SD was 0.225 ± 0.115 in A-RIR and 0.196 ± 0.114 in H-RIR (P <0.001). The absolute translational error was 0.38 ± 0.31 mm. The rotational error was 0.03 ± 0.20, 0.05 ± 0.19, 0.04 ± 0.20 degrees in axial, coronal, and sagittal planes (range: 0.66–0.52).

Conclusion

A-RIR shows non-inferior to H-RIR in CT and CT-myelogram registration for postoperative spine SBRT planning.