@MASTERSTHESIS\{IMM2012-06404, author = "S. C. Claessen", title = "Adaptive Radiotherapy - {CBCT} Based Dose Calculation", year = "2012", school = "Technical University of Denmark, {DTU} Informatics, {E-}mail: reception@imm.dtu.dk", address = "Asmussens Alle, Building 305, {DK-}2800 Kgs. Lyngby, Denmark", type = "", note = "Supervisors: Claus Behrens, David Sj{\"{o}}str{\"{o}}m, Eva Emma Maria Sj{\"{o}}lin, and Rasmus R. Poulsen, rrp@imm.dtu.dk, {DTU} Informatics", url = "http://www.imm.dtu.dk/English.aspx", abstract = "Background: The aim of this report is to evaluate, if {CBCT} can be used for dose calculation. The advantage in using {CBCT} for dose calculation, is to be able to predict and assess the dose delivered to the patient on a daily basis. Materials \& Methods: The study was subdivided into three parts. Part A: Various scan parameters and phantom con gurations were investigated for their impact on the Houns eld units (HUs) for Computed tomography (CT) and {CBCT}. For this investigation a {CIRS} water equivalent electron density phantom (DP) was used. The di fferent confi gurations of the {DP} were used to obtain HUrelative electron density calibration curves. The {CT} curve from the {CT} scan obtained with clinic standard parameters (CTS) was used as reference. Part B: The default and the obtained calibration curves from the different {CBCT} protocols were selected for the dose calculation on the {CBCT} images. Using the Alderson phantom it was investigated which protocol and calibration curve was the most appropriate for the {CBCT} based dose calculation. Part C: The results from the Alderson (ARP) study were evaluated in a clinical perspective on an head and neck patient (H\&N) treated with intensity-modulated radiotherapy. In order to investigate if a site-specifi c calibration curve for di fferent patient groups was needed di fferent calibration curves were used for the head and neck patient. The calibration curves obtained from the pelvis con figuration on {DP} were used to calculate the dose distribution on the pelvis patient treated with rapid arc. The intention was to investigate if {CBCT} can be used for dose calculation for this patient group. Results: Part A: Compared to {CT} it was found, that the HUs from {CBCT} were more easily a ffected when changing the scan parameters. Voltage, {DP} size and insert arrangements aff ect the HUs the most. Part B: The {ARP} study showed a maximum dose di fference of 0.6\% when comparing the use of the {CTS} and the default calibration curve. The most appropriate {CBCT} based dose calculation was achieved with the standard dose head protocol. A 0.3\% maximum dose di fference between {CBCT} and {CT} was found. It was found that further investigation is needed in order to evaluate whether the {CBCT} or the {CT} calibration curve achieves the most accurate {CBCT} based dose calculation. Part C: For the H\&N patient a 1.7\% maximum dose di fference between using the {CTS} and the default calibration curve was detected. A maximum dose di fference between {CT} and {CBCT} was found to be 0.3\%. As for the {ARP} study, a further investigation is needed in order to evaluate whether the {CBCT} or the {CT} calibration curve achieves the most accurate {CBCT} based dose calculation. The results for cervix showed that further investigation was needed to conclude whether {CBCT} can be used for dose calculation on cervix patients. Further it was found that using a site-specifi c calibration curve for di fferent patient groups achieved a {CBCT} based dose distribution most similar to the {CT} based dose distribution. Conclusion: It is concluded that {CBCT} can be used for dose calculation on H\&N patients, but that further investigation is needed for the cervix patient. The standard protocol for {CBCT} is shown the to achieve a dose calculation similar to that of {CT} for the H\&N patient. Also, it is concluded that the use of site-specifi c calibration curve is needed in order to calculate an accurate dose distribution on {CBCT}." }