2110 - Clinical Experience with a CT-Free CBCT-Guided Online Adaptive Workflow for Palliative Radiotherapy
Presenter(s)
A. T. Jaglal1,2, K. J. Nelissen1,2, A. R. W. van Vlaenderen1,2, A. L. de la Fuente1,2, W. F. A. R. Verbakel1,3, F. L. Schneiders1,2, P. S. N. van Rossum1,2, J. Wiersma1,2, S. Senan1,2, E. Versteijne1,2, and J. Visser4,5; 1Amsterdam UMC location Vrije Universiteit Amsterdam, Department of Radiation Oncology, Amsterdam, Netherlands, 2Cancer Center Amsterdam, Amsterdam, Netherlands, 3Varian, a Siemens Healthineers Company, Palo Alto, CA, 4Cancer Center Amsterdam, Cancer Therapy, Treatment and quality of life, Amsterdam, Netherlands, 5Radiation Oncology, Amsterdam UMC location University of Amsterdam, Meibergdreef 9, Amsterdam, Netherlands
Purpose/Objective(s):
Online adaptive radiotherapy (oART) for palliative treatments was implemented at our department in 2022 through the FAST-METS study, using the diagnostic CT for initial planning. Introduction of upgraded software and hardware have enabled a CT-free workflow using on-couch contouring, dose calculation, and optimization on the CBCT. This study presents the first clinical experiences with this CT-free, CBCT-guided oART workflow for palliative radiotherapy.Materials/Methods:
In this study, we evaluated two different clinical CT-free oART workflows. In both workflows a cylindrical water phantom (40×80 cm, diameter × length) was used to meet software constraints requiring an initial plan with a predefined template and beam setup before CBCT-based adaptation. Workflow 1 incorporated pre-treatment imaging (diagnostic CT or MRI) for initial clinical target volume (CTV) contouring. The CTV was transferred to the phantom and rigidly mapped to the CBCT on-couch and serving as an intermediate step to Workflow 2, where the CTV was directly contoured on-couch on the CBCT. Both workflows utilized a standardized planning template for all treatment sites with a generic lateral 7-field or 9-field IMRT beam setup, depending on the target site. Organs-at-risk (OARs) were delineated using AI-based auto-contouring. Clinical dose coverage goals (V95%) for both CTV and planning target volume (PTV) were assessed for each patient, along with workflow efficiency, including the time spent in different stages of the treatment.Results:
Thirteen patients were included, with treated locations in the cervical (n=1), thoracic (n=5), lumbar (n=2), and pelvic (n=5) regions. For ten patients, diagnostic CT-based contours (n=9) or MRI-based contours (n=1) were transferred to the phantom (Workflow 1). Three patients received treatment without initial contouring (Workflow 2). Both oART workflows successfully achieved the defined clinical goals, with PTV V95% = 98.6%, and CTV V95% = 100%. The overall treatment time was similar to that with the previous FAST-METS workflow, with a median treatment time of 31 minutes (range: 24—43) from patient entry to exit. Detailed times for the treatment stages are summarized in Table 1.Conclusion:
This study demonstrates the clinical feasibility of fully CT-free workflows for palliative radiotherapy utilizing on-couch CBCT-based contouring and dose calculation. A CT-free workflow enabled efficient treatment delivery, requiring only a single departmental visit, and a median in-room time of 31 minutes. The use of a standardized planning template and CBCT-guided adaptation facilitated rapid and safe patient care, making this workflow attractive for emergency cases. Abstract 2110 - Table 1: Median and range of treatment stage times| Treatment stage | Median [range] (minutes:seconds) |
| Setup | 6:54 [4:41 —12:24] |
| Contouring | 5:07 [3:31 —18:50] |
| Calculation | 1:57 [1:39 —2:44] |
| Plan evaluation | 3:29 [2:44 —4:30] |
| Treatment delivery and patient exit | 8:18 [5:23 —10:03] |