Clinical Implementation of Lung SABR IMPT Using Two PBS Systems With Different Spot Sizes and Delivery Speeds

Stereotactic Ablative Body Therapy (SABR) is an effective treatment for early-stage lung cancer. Two different proton therapy delivery systems (Proteous-plus with universal nozzle called P+ and Proteus-one called P1) were employed to test the spot size difference, plan dosimetric quality, and delive...

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Published inInternational journal of radiation oncology, biology, physics Vol. 111; no. 3; pp. e549 - e550
Main Authors Su, Z., Hsi, W.C., Brooks, E.
Format Journal Article
LanguageEnglish
Published Elsevier Inc 01.11.2021
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Abstract Stereotactic Ablative Body Therapy (SABR) is an effective treatment for early-stage lung cancer. Two different proton therapy delivery systems (Proteous-plus with universal nozzle called P+ and Proteus-one called P1) were employed to test the spot size difference, plan dosimetric quality, and delivery time needed for practical and effective clinical treatment. Total of 9 lung patients with 10 tumors were selected for this study. Seven targets were prescribed 60 Gy in 10 fractions; three patients were 48 Gy in 4 fractions. A treatment planning system was used to generate treatment plans for each nozzle type with exact same optimization objectives. P1 plans used 4cm range-shifter placed at 45cm from isocenter to create large in-air beam spots to mimic P+ system. The spot sizes were compared to the P+ in-air spots without range shifter. P+ plans used 7cm range-shifter placed very close to patients, i.e., 4cm away, to minimize spot size degradation. Target coverage was optimized and normalized to prescription dose cover 100-percent of GTV and 90-percent covers PTV. Dose to the OARs were compared using QUANTEC metrics. Each plan was split into three subsets to perform volumetric dose-repainting to reduce interplay effect. The plan beam-on times of both systems were obtained to evaluate treatment delivery efficiency and impact of patient comfort. The in-air beam spots were comparable between the P+ without and P1 with range shifter. All PTVs were covered by 90-percent prescription dose. OAR doses were comparable and within the QUANTEC limits. The beam-on time of P+ plans are 3 to 6 time of those of P1 plans. When combined with patient setup and image guidance, patient discomfort could lead to higher uncertainty in P+ treatment. P1 system with 45cm away from isocenter can effectively simulate a large spot PBS system, P+. Lung SABR IMPT plan qualities between the two systems were dosimetrically comparable. Volumetric dose-repainting were applicable to both systems to reduce interplay effect. However, the plan beam-on and delivery time of P1 system were significantly shorter than that of P+. Therefore, potential less patient movement during treatment leads to less dose uncertainties to patients.
AbstractList Stereotactic Ablative Body Therapy (SABR) is an effective treatment for early-stage lung cancer. Two different proton therapy delivery systems (Proteous-plus with universal nozzle called P+ and Proteus-one called P1) were employed to test the spot size difference, plan dosimetric quality, and delivery time needed for practical and effective clinical treatment. Total of 9 lung patients with 10 tumors were selected for this study. Seven targets were prescribed 60 Gy in 10 fractions; three patients were 48 Gy in 4 fractions. A treatment planning system was used to generate treatment plans for each nozzle type with exact same optimization objectives. P1 plans used 4cm range-shifter placed at 45cm from isocenter to create large in-air beam spots to mimic P+ system. The spot sizes were compared to the P+ in-air spots without range shifter. P+ plans used 7cm range-shifter placed very close to patients, i.e., 4cm away, to minimize spot size degradation. Target coverage was optimized and normalized to prescription dose cover 100-percent of GTV and 90-percent covers PTV. Dose to the OARs were compared using QUANTEC metrics. Each plan was split into three subsets to perform volumetric dose-repainting to reduce interplay effect. The plan beam-on times of both systems were obtained to evaluate treatment delivery efficiency and impact of patient comfort. The in-air beam spots were comparable between the P+ without and P1 with range shifter. All PTVs were covered by 90-percent prescription dose. OAR doses were comparable and within the QUANTEC limits. The beam-on time of P+ plans are 3 to 6 time of those of P1 plans. When combined with patient setup and image guidance, patient discomfort could lead to higher uncertainty in P+ treatment. P1 system with 45cm away from isocenter can effectively simulate a large spot PBS system, P+. Lung SABR IMPT plan qualities between the two systems were dosimetrically comparable. Volumetric dose-repainting were applicable to both systems to reduce interplay effect. However, the plan beam-on and delivery time of P1 system were significantly shorter than that of P+. Therefore, potential less patient movement during treatment leads to less dose uncertainties to patients.
Author Hsi, W.C.
Su, Z.
Brooks, E.
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  organization: Department of Radiation Oncology, University of Florida College of Medicine, Jacksonville, FL
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