Jue Jiang, Chloe Min Seo Choi, Maria Thor, Joseph O. Deasy, Harini Veeraraghavan
{"title":"肺癌计算机断层扫描患者间可变形图像配准的肿瘤感知复发。","authors":"Jue Jiang, Chloe Min Seo Choi, Maria Thor, Joseph O. Deasy, Harini Veeraraghavan","doi":"10.1002/mp.17536","DOIUrl":null,"url":null,"abstract":"<div>\n \n \n <section>\n \n <h3> Background</h3>\n \n <p>Voxel-based analysis (VBA) for population level radiotherapy (RT) outcomes modeling requires topology preserving inter-patient deformable image registration (DIR) that preserves tumors on moving images while avoiding unrealistic deformations due to tumors occurring on fixed images.</p>\n </section>\n \n <section>\n \n <h3> Purpose</h3>\n \n <p>We developed a <span>t</span>umo<span>r</span>-<span>a</span>ware re<span>c</span>urr<span>e</span>nt <span>r</span>egistration (TRACER) deep learning (DL) method and evaluated its suitability for VBA.</p>\n </section>\n \n <section>\n \n <h3> Methods</h3>\n \n <p>TRACER consists of encoder layers implemented with stacked 3D convolutional long short term memory network (3D-CLSTM) followed by decoder and spatial transform layers to compute dense deformation vector field (DVF). Multiple CLSTM steps are used to compute a progressive sequence of deformations. Input conditioning was applied by including tumor segmentations with 3D image pairs as input channels. Bidirectional tumor rigidity, image similarity, and deformation smoothness losses were used to optimize the network in an unsupervised manner. TRACER and multiple DL methods were trained with 204 3D computed tomography (CT) image pairs from patients with lung cancers (LC) and evaluated using (a) Dataset I (<i>N</i> = 308 pairs) with DL segmented LCs, (b) Dataset II (<i>N</i> = 765 pairs) with manually delineated LCs, and (c) Dataset III with 42 LC patients treated with RT.</p>\n </section>\n \n <section>\n \n <h3> Results</h3>\n \n <p>TRACER accurately aligned normal tissues. It best preserved tumors, indicated by the smallest tumor volume difference of 0.24%, 0.40%, and 0.13 % and mean square error in CT intensities of 0.005, 0.005, 0.004, computed between original and resampled moving image tumors, for Datasets I, II, and III, respectively. It resulted in the smallest planned RT tumor dose difference computed between original and resampled moving images of 0.01 and 0.013 Gy when using a female and a male reference.</p>\n </section>\n \n <section>\n \n <h3> Conclusions</h3>\n \n <p>TRACER is a suitable method for inter-patient registration involving LC occurring in both fixed and moving images and applicable to voxel-based analysis methods.</p>\n </section>\n </div>","PeriodicalId":18384,"journal":{"name":"Medical physics","volume":"52 2","pages":"938-950"},"PeriodicalIF":3.2000,"publicationDate":"2024-11-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Tumor aware recurrent inter-patient deformable image registration of computed tomography scans with lung cancer\",\"authors\":\"Jue Jiang, Chloe Min Seo Choi, Maria Thor, Joseph O. 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Multiple CLSTM steps are used to compute a progressive sequence of deformations. Input conditioning was applied by including tumor segmentations with 3D image pairs as input channels. Bidirectional tumor rigidity, image similarity, and deformation smoothness losses were used to optimize the network in an unsupervised manner. TRACER and multiple DL methods were trained with 204 3D computed tomography (CT) image pairs from patients with lung cancers (LC) and evaluated using (a) Dataset I (<i>N</i> = 308 pairs) with DL segmented LCs, (b) Dataset II (<i>N</i> = 765 pairs) with manually delineated LCs, and (c) Dataset III with 42 LC patients treated with RT.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Results</h3>\\n \\n <p>TRACER accurately aligned normal tissues. 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Tumor aware recurrent inter-patient deformable image registration of computed tomography scans with lung cancer
Background
Voxel-based analysis (VBA) for population level radiotherapy (RT) outcomes modeling requires topology preserving inter-patient deformable image registration (DIR) that preserves tumors on moving images while avoiding unrealistic deformations due to tumors occurring on fixed images.
Purpose
We developed a tumor-aware recurrent registration (TRACER) deep learning (DL) method and evaluated its suitability for VBA.
Methods
TRACER consists of encoder layers implemented with stacked 3D convolutional long short term memory network (3D-CLSTM) followed by decoder and spatial transform layers to compute dense deformation vector field (DVF). Multiple CLSTM steps are used to compute a progressive sequence of deformations. Input conditioning was applied by including tumor segmentations with 3D image pairs as input channels. Bidirectional tumor rigidity, image similarity, and deformation smoothness losses were used to optimize the network in an unsupervised manner. TRACER and multiple DL methods were trained with 204 3D computed tomography (CT) image pairs from patients with lung cancers (LC) and evaluated using (a) Dataset I (N = 308 pairs) with DL segmented LCs, (b) Dataset II (N = 765 pairs) with manually delineated LCs, and (c) Dataset III with 42 LC patients treated with RT.
Results
TRACER accurately aligned normal tissues. It best preserved tumors, indicated by the smallest tumor volume difference of 0.24%, 0.40%, and 0.13 % and mean square error in CT intensities of 0.005, 0.005, 0.004, computed between original and resampled moving image tumors, for Datasets I, II, and III, respectively. It resulted in the smallest planned RT tumor dose difference computed between original and resampled moving images of 0.01 and 0.013 Gy when using a female and a male reference.
Conclusions
TRACER is a suitable method for inter-patient registration involving LC occurring in both fixed and moving images and applicable to voxel-based analysis methods.
期刊介绍:
Medical Physics publishes original, high impact physics, imaging science, and engineering research that advances patient diagnosis and therapy through contributions in 1) Basic science developments with high potential for clinical translation 2) Clinical applications of cutting edge engineering and physics innovations 3) Broadly applicable and innovative clinical physics developments
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