C00-C97
Conditions
Interventions
Group 1: In the standard (control) group, target volume (GTV) and organs-at-risk (OAR) delineation during the initial treatment planning are performed using conventional manual contouring methods as p
Sponsors
LMU Klinikum
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Patients undergoing MR-guided radiotherapy for lesions in the thorax, abdomen or pelvis at the Department of Radiation Oncology of the LMU University Hospital and providing informed written consent will be included in this study.
Exclusion criteria
Exclusion criteria: None.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary outcome is the reduction in the time required to reach clinically acceptable delineations during treatment planning in MR-guided radiotherapy compared to standard manual methods. | — |
Secondary
| Measure | Time frame |
|---|---|
| Quantitative agreement between AI-assissted generated and final physician-approved OAR segmentations (Dice Similarity Coefficient (DSC), surface distances, surface DSC, normalized added path length), as well as user satisfaction assessed using the System Usability Scale (SUS). | — |
Countries
Germany
Contacts
Public ContactStefanie Corradini
LMU Klinikum
Outcome results
None listed