SU‐E‐J‐151: Evaluation of a Real Time Tumour Autocontouring Algorithm Using In‐Vivo Lung MR Images with Various Contrast to Noise Ratios

Purpose: To quantitatively evaluate a lung tumour autocontouring algorithm using in‐vivo lung cancer patient MR images with varying contrast to noise ratios (CNR) simulating images acquired at various MR field strengths. Methods: A non small cell lung cancer patient with posterior lung tumour is ima...

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Veröffentlicht in:Medical Physics 2012-06, Vol.39 (6), p.3687-3687
Hauptverfasser: Yip, E, Yun, J, Gabos, Z, Wachowicz, K, Rathee, S, Fallone, B
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container_end_page 3687
container_issue 6
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container_title Medical Physics
container_volume 39
creator Yip, E
Yun, J
Gabos, Z
Wachowicz, K
Rathee, S
Fallone, B
description Purpose: To quantitatively evaluate a lung tumour autocontouring algorithm using in‐vivo lung cancer patient MR images with varying contrast to noise ratios (CNR) simulating images acquired at various MR field strengths. Methods: A non small cell lung cancer patient with posterior lung tumour is imaged (sagittal plane) in a 3T MRI using a dynamic bSSFP sequence (FOV: 40×40cm2, voxel size: 3.1×3.1x20mm3, TE = 1.1ms. TR = 2.2ms, 275ms per image) under free breathing for approximately 3 minutes (650 images). Gaussian random noise is added to the 3T images to approximately simulate the equivalent CNR in images acquired at 1.5T, 1.0T, 0.5T, 0.3T and 0.2T. The moving tumour in all 3T images is contoured by a physician for reference. The first 20 of these manual contours are used for the parameters optimization of auto‐contouring algorithm. The automatic contours from the remaining images are quantitatively compared with the physician's contours using the centroid's displacement and the Dice's coefficient (DC). Results: The oncologist's contours of the 3T images show a maximum S‐I motion of 26mm. Compared to the oncologist's contours, automatic contours have an average centroid displacement of 1.37mm, and an average DC of 0.881. The autocontouring algorithm's performance with images in the range of 1.5T to 0.5T equivalent CNRs is similar to that of the 3T data. However, for the lowest CNR datasets (0.2, 0.3T) an increase in centroid displacement and decrease in DC is observed, with mean displacements of 1.56mm, 1.71mm and DCs of 0.870, 0.836 for the 0.3T and 0.2T dataset, respectivelyConclusions: With in‐vivo MR images, the autocontouring algorithm generated lung tumour contours similar to ones drawn by a physician (DC 〉 0.83). In this patient, additional CNR from 〉0.5T MRIs does not provide statistically significant improvement in the accuracy of our autocontouring software. E.Yip is supported by the Canadian Institutes of Health Research as well as Alberta Innovates ‐ Health Solutions
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Methods: A non small cell lung cancer patient with posterior lung tumour is imaged (sagittal plane) in a 3T MRI using a dynamic bSSFP sequence (FOV: 40×40cm2, voxel size: 3.1×3.1x20mm3, TE = 1.1ms. TR = 2.2ms, 275ms per image) under free breathing for approximately 3 minutes (650 images). Gaussian random noise is added to the 3T images to approximately simulate the equivalent CNR in images acquired at 1.5T, 1.0T, 0.5T, 0.3T and 0.2T. The moving tumour in all 3T images is contoured by a physician for reference. The first 20 of these manual contours are used for the parameters optimization of auto‐contouring algorithm. The automatic contours from the remaining images are quantitatively compared with the physician's contours using the centroid's displacement and the Dice's coefficient (DC). Results: The oncologist's contours of the 3T images show a maximum S‐I motion of 26mm. Compared to the oncologist's contours, automatic contours have an average centroid displacement of 1.37mm, and an average DC of 0.881. The autocontouring algorithm's performance with images in the range of 1.5T to 0.5T equivalent CNRs is similar to that of the 3T data. However, for the lowest CNR datasets (0.2, 0.3T) an increase in centroid displacement and decrease in DC is observed, with mean displacements of 1.56mm, 1.71mm and DCs of 0.870, 0.836 for the 0.3T and 0.2T dataset, respectivelyConclusions: With in‐vivo MR images, the autocontouring algorithm generated lung tumour contours similar to ones drawn by a physician (DC 〉 0.83). In this patient, additional CNR from 〉0.5T MRIs does not provide statistically significant improvement in the accuracy of our autocontouring software. 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Methods: A non small cell lung cancer patient with posterior lung tumour is imaged (sagittal plane) in a 3T MRI using a dynamic bSSFP sequence (FOV: 40×40cm2, voxel size: 3.1×3.1x20mm3, TE = 1.1ms. TR = 2.2ms, 275ms per image) under free breathing for approximately 3 minutes (650 images). Gaussian random noise is added to the 3T images to approximately simulate the equivalent CNR in images acquired at 1.5T, 1.0T, 0.5T, 0.3T and 0.2T. The moving tumour in all 3T images is contoured by a physician for reference. The first 20 of these manual contours are used for the parameters optimization of auto‐contouring algorithm. The automatic contours from the remaining images are quantitatively compared with the physician's contours using the centroid's displacement and the Dice's coefficient (DC). Results: The oncologist's contours of the 3T images show a maximum S‐I motion of 26mm. Compared to the oncologist's contours, automatic contours have an average centroid displacement of 1.37mm, and an average DC of 0.881. The autocontouring algorithm's performance with images in the range of 1.5T to 0.5T equivalent CNRs is similar to that of the 3T data. However, for the lowest CNR datasets (0.2, 0.3T) an increase in centroid displacement and decrease in DC is observed, with mean displacements of 1.56mm, 1.71mm and DCs of 0.870, 0.836 for the 0.3T and 0.2T dataset, respectivelyConclusions: With in‐vivo MR images, the autocontouring algorithm generated lung tumour contours similar to ones drawn by a physician (DC 〉 0.83). In this patient, additional CNR from 〉0.5T MRIs does not provide statistically significant improvement in the accuracy of our autocontouring software. 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Methods: A non small cell lung cancer patient with posterior lung tumour is imaged (sagittal plane) in a 3T MRI using a dynamic bSSFP sequence (FOV: 40×40cm2, voxel size: 3.1×3.1x20mm3, TE = 1.1ms. TR = 2.2ms, 275ms per image) under free breathing for approximately 3 minutes (650 images). Gaussian random noise is added to the 3T images to approximately simulate the equivalent CNR in images acquired at 1.5T, 1.0T, 0.5T, 0.3T and 0.2T. The moving tumour in all 3T images is contoured by a physician for reference. The first 20 of these manual contours are used for the parameters optimization of auto‐contouring algorithm. The automatic contours from the remaining images are quantitatively compared with the physician's contours using the centroid's displacement and the Dice's coefficient (DC). Results: The oncologist's contours of the 3T images show a maximum S‐I motion of 26mm. Compared to the oncologist's contours, automatic contours have an average centroid displacement of 1.37mm, and an average DC of 0.881. The autocontouring algorithm's performance with images in the range of 1.5T to 0.5T equivalent CNRs is similar to that of the 3T data. However, for the lowest CNR datasets (0.2, 0.3T) an increase in centroid displacement and decrease in DC is observed, with mean displacements of 1.56mm, 1.71mm and DCs of 0.870, 0.836 for the 0.3T and 0.2T dataset, respectivelyConclusions: With in‐vivo MR images, the autocontouring algorithm generated lung tumour contours similar to ones drawn by a physician (DC 〉 0.83). In this patient, additional CNR from 〉0.5T MRIs does not provide statistically significant improvement in the accuracy of our autocontouring software. 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subjects Cancer
Computer software
Lungs
Magnetic resonance imaging
Medical image noise
Medical imaging
Medical magnetic resonance imaging
Random noise
title SU‐E‐J‐151: Evaluation of a Real Time Tumour Autocontouring Algorithm Using In‐Vivo Lung MR Images with Various Contrast to Noise Ratios
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