Patterns of practice for adaptive and real-time radiation therapy (POP-ART RT) part II: Offline and online plan adaption for interfractional changes.
Jenny Bertholet, Gail Anastasi, David Noble...
https://pubmed.ncbi.nlm.nih.gov/32579998Actively Recruiting
Led by Universitaire Ziekenhuizen KU Leuven · Updated on 2025-12-02
30
Participants Needed
1
Research Sites
21 weeks
Total Duration
Locally advanced non-small cell lung cancer (LA-NSCLC) is a common and deadly form of lung cancer often treated with a combination of systemic therapy, radiotherapy, and immunotherapy. Researchers are studying adaptive radiotherapy (ART), which adjusts treatment plans during radiotherapy to account for tumor and anatomical changes, potentially improving survival. This trial focuses on improving the efficiency of ART by using modern AI tools and advanced imaging to reduce labor and patient burden. The study involves a prospective phase where 30 patients undergo mid-treatment plan adaptations using repeated four-dimensional CT scans and AI-assisted contouring and planning tools, such as Syngo.via® and RapidPlan®. A retrospective phase will then evaluate the feasibility of using cone-beam CT (CBCT) imaging, routinely used for position verification, as a replacement for repeated planning CTs. This approach aims to reduce additional radiation exposure and appointments by generating synthetic CTs from CBCT images for treatment adaptation. Participants will have repeated imaging and treatment plan adjustments during their radiotherapy course, which lasts up to seven weeks. Researchers will measure the time required for each step of the ART workflow, compare treatment plan quality using dose-volume histograms, and assess contour accuracy with similarity metrics. The study also includes quality checks by medical physicists and physicians. The retrospective phase will analyze the performance of the CBCT-based workflow up to six months after treatment completion.
CONDITIONS
Efficiency of Contemporary Off-line Adaptive Radiotherapy for Lung Cancer
You may qualify if you...
You will not qualify if you...
Complete this quick 3-step screening to check your eligibility
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Up to 7 weeks
Participants receive daily radiotherapy treatments over a period of up to seven weeks. Mid-treatment, participants undergo a repeated planning CT scan with updated contouring and treatment planning to adapt the radiotherapy plan according to anatomical changes.
Daily visits for radiotherapy with a mid-treatment repeated planning CT and adaptive planning session
Duration - Up to 6 months
After completing radiotherapy, participants are retrospectively evaluated for a CBCT-based adaptive radiotherapy workflow using imaging collected during treatment. This retrospective phase assesses the feasibility and efficiency of using CBCT imaging for adaptive planning.
No additional visits; retrospective analysis of imaging and planning data
Total: 1 location
1
UZ Leuven
Leuven, Vlaams-Brabant, Belgium, 3000
Actively Recruiting
W
Wouter Crijns, Prof. Dr.
M
Maarten Lambrecht, Prof. Dr.
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
TREATMENT
Number of Arms
1
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