Xueyan Tang, Hok Wan Chan Tseung, Mark D. Pepin, Jed E. Johnson, Doug J. Moseley, David M. Routman, Jing Qian
{"title":"带变压器的质子剂量计算:将点图转换为剂量。","authors":"Xueyan Tang, Hok Wan Chan Tseung, Mark D. Pepin, Jed E. Johnson, Doug J. Moseley, David M. Routman, Jing Qian","doi":"10.1002/mp.17794","DOIUrl":null,"url":null,"abstract":"<div>\n \n \n <section>\n \n <h3> Background</h3>\n \n <p>Conventional proton dose calculation methods are either time- and resource-intensive, like Monte Carlo (MC) simulations, or they sacrifice accuracy, as seen with analytical methods. This trade-off between computational efficiency and accuracy highlights the need for improved dose calculation approaches in clinical settings.</p>\n </section>\n \n <section>\n \n <h3> Purpose</h3>\n \n <p>This study aims to develop a deep-learning-based model that calculates dose-to-water (<i>D</i><sub>W</sub>) and dose-to-medium (<i>D</i><sub>M</sub>) using patient anatomy and proton spot map (PSM), achieving approaching MC-level accuracy with significantly reduced computation time. Additionally, the study seeks to generalize the model to different treatment sites using transfer learning.</p>\n </section>\n \n <section>\n \n <h3> Methods</h3>\n \n <p>A SwinUNetr model was developed using 259 four-field prostate proton stereotactic body radiation therapy (SBRT) plans to calculate patient-specific <i>D</i><sub>W</sub> and <i>D</i><sub>M</sub> distributions from CT and projected PSM (PPSM). The PPSM was created by projecting PSM into the CT scans using spot coordinates, stopping power ratio, beam divergence, and water-equivalent thickness. Fine-tuning was then performed for the central nervous system (CNS) site using 84 CNS plans. The model's accuracy was evaluated against MC simulation benchmarks using mean absolute error (MAE), gamma analysis (2% local dose difference, 2-mm distance-to-agreement, 10% low dose threshold), and relevant clinical indices on the test dataset.</p>\n </section>\n \n <section>\n \n <h3> Results</h3>\n \n <p>The trained model achieved a single-field dose calculation time of 0.07 s on a Nvidia-A100 GPU, over 100 times faster than MC simulators. For the prostate site, the best-performing model showed an average MAE of 0.26 ± 0.17 Gy and a gamma index of 92.2% ± 3.1% in dose regions above 10% of the maximum dose for <i>D</i><sub>W</sub> calculations, and an MAE of 0.30 ± 0.19 Gy with a gamma index of 89.7% ± 3.9% for <i>D</i><sub>M</sub> calculations. After transfer learning for CNS plans, the model achieved an MAE of 0.49 ± 0.24 Gy and a gamma index of 90.1% ± 2.7% for <i>D</i><sub>W</sub> computations, and an MAE of 0.47 ± 0.25 Gy with a gamma index of 85.4% ± 7.1% for <i>D</i><sub>M</sub> computations.</p>\n </section>\n \n <section>\n \n <h3> Conclusions</h3>\n \n <p>The SwinUNetr model provides an efficient and accurate method for computing dose distributions in proton therapy. It also opens the possibility of reverse-engineering PSM from <i>D</i><sub>W</sub>, potentially speeding up treatment planning while maintaining accuracy.</p>\n </section>\n </div>","PeriodicalId":18384,"journal":{"name":"Medical physics","volume":"52 6","pages":"4941-4952"},"PeriodicalIF":3.2000,"publicationDate":"2025-03-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Proton dose calculation with transformer: Transforming spot map to dose\",\"authors\":\"Xueyan Tang, Hok Wan Chan Tseung, Mark D. Pepin, Jed E. Johnson, Doug J. Moseley, David M. Routman, Jing Qian\",\"doi\":\"10.1002/mp.17794\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div>\\n \\n \\n <section>\\n \\n <h3> Background</h3>\\n \\n <p>Conventional proton dose calculation methods are either time- and resource-intensive, like Monte Carlo (MC) simulations, or they sacrifice accuracy, as seen with analytical methods. This trade-off between computational efficiency and accuracy highlights the need for improved dose calculation approaches in clinical settings.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Purpose</h3>\\n \\n <p>This study aims to develop a deep-learning-based model that calculates dose-to-water (<i>D</i><sub>W</sub>) and dose-to-medium (<i>D</i><sub>M</sub>) using patient anatomy and proton spot map (PSM), achieving approaching MC-level accuracy with significantly reduced computation time. Additionally, the study seeks to generalize the model to different treatment sites using transfer learning.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Methods</h3>\\n \\n <p>A SwinUNetr model was developed using 259 four-field prostate proton stereotactic body radiation therapy (SBRT) plans to calculate patient-specific <i>D</i><sub>W</sub> and <i>D</i><sub>M</sub> distributions from CT and projected PSM (PPSM). The PPSM was created by projecting PSM into the CT scans using spot coordinates, stopping power ratio, beam divergence, and water-equivalent thickness. Fine-tuning was then performed for the central nervous system (CNS) site using 84 CNS plans. The model's accuracy was evaluated against MC simulation benchmarks using mean absolute error (MAE), gamma analysis (2% local dose difference, 2-mm distance-to-agreement, 10% low dose threshold), and relevant clinical indices on the test dataset.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Results</h3>\\n \\n <p>The trained model achieved a single-field dose calculation time of 0.07 s on a Nvidia-A100 GPU, over 100 times faster than MC simulators. For the prostate site, the best-performing model showed an average MAE of 0.26 ± 0.17 Gy and a gamma index of 92.2% ± 3.1% in dose regions above 10% of the maximum dose for <i>D</i><sub>W</sub> calculations, and an MAE of 0.30 ± 0.19 Gy with a gamma index of 89.7% ± 3.9% for <i>D</i><sub>M</sub> calculations. After transfer learning for CNS plans, the model achieved an MAE of 0.49 ± 0.24 Gy and a gamma index of 90.1% ± 2.7% for <i>D</i><sub>W</sub> computations, and an MAE of 0.47 ± 0.25 Gy with a gamma index of 85.4% ± 7.1% for <i>D</i><sub>M</sub> computations.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Conclusions</h3>\\n \\n <p>The SwinUNetr model provides an efficient and accurate method for computing dose distributions in proton therapy. It also opens the possibility of reverse-engineering PSM from <i>D</i><sub>W</sub>, potentially speeding up treatment planning while maintaining accuracy.</p>\\n </section>\\n </div>\",\"PeriodicalId\":18384,\"journal\":{\"name\":\"Medical physics\",\"volume\":\"52 6\",\"pages\":\"4941-4952\"},\"PeriodicalIF\":3.2000,\"publicationDate\":\"2025-03-29\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Medical physics\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/mp.17794\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Medical physics","FirstCategoryId":"3","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/mp.17794","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING","Score":null,"Total":0}
Proton dose calculation with transformer: Transforming spot map to dose
Background
Conventional proton dose calculation methods are either time- and resource-intensive, like Monte Carlo (MC) simulations, or they sacrifice accuracy, as seen with analytical methods. This trade-off between computational efficiency and accuracy highlights the need for improved dose calculation approaches in clinical settings.
Purpose
This study aims to develop a deep-learning-based model that calculates dose-to-water (DW) and dose-to-medium (DM) using patient anatomy and proton spot map (PSM), achieving approaching MC-level accuracy with significantly reduced computation time. Additionally, the study seeks to generalize the model to different treatment sites using transfer learning.
Methods
A SwinUNetr model was developed using 259 four-field prostate proton stereotactic body radiation therapy (SBRT) plans to calculate patient-specific DW and DM distributions from CT and projected PSM (PPSM). The PPSM was created by projecting PSM into the CT scans using spot coordinates, stopping power ratio, beam divergence, and water-equivalent thickness. Fine-tuning was then performed for the central nervous system (CNS) site using 84 CNS plans. The model's accuracy was evaluated against MC simulation benchmarks using mean absolute error (MAE), gamma analysis (2% local dose difference, 2-mm distance-to-agreement, 10% low dose threshold), and relevant clinical indices on the test dataset.
Results
The trained model achieved a single-field dose calculation time of 0.07 s on a Nvidia-A100 GPU, over 100 times faster than MC simulators. For the prostate site, the best-performing model showed an average MAE of 0.26 ± 0.17 Gy and a gamma index of 92.2% ± 3.1% in dose regions above 10% of the maximum dose for DW calculations, and an MAE of 0.30 ± 0.19 Gy with a gamma index of 89.7% ± 3.9% for DM calculations. After transfer learning for CNS plans, the model achieved an MAE of 0.49 ± 0.24 Gy and a gamma index of 90.1% ± 2.7% for DW computations, and an MAE of 0.47 ± 0.25 Gy with a gamma index of 85.4% ± 7.1% for DM computations.
Conclusions
The SwinUNetr model provides an efficient and accurate method for computing dose distributions in proton therapy. It also opens the possibility of reverse-engineering PSM from DW, potentially speeding up treatment planning while maintaining accuracy.
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
Medical Physics is a journal of global scope and reach. By publishing in Medical Physics your research will reach an international, multidisciplinary audience including practicing medical physicists as well as physics- and engineering based translational scientists. We work closely with authors of promising articles to improve their quality.