Lung Neoplasm Clinical Trial
— VENTUREOfficial title:
Ventilation Using Radiographic Examination: Functional Lung Imaging Techniques for the Reduction of Toxicity in Functional Avoidance Radiation Therapy
The goal of this observational validation study is to determine the best implementation of fluoroscopic and CT ventilation imaging in patients having non-stereotactic ablative body radiotherapy (non-SABR) radiotherapy for stages II-IV lung cancer. The main questions it aims to answer are: - Assess the dosimetric variation in functional avoidance radiation therapy (RT) plans produced using these ventilation imaging techniques, - Establish a quality assurance procedure for functional lung avoidance radiation therapy, and - Evaluate the clinical acceptable thresholds for accuracy of the method. Participants will: Prior to radiation therapy treatment, patients will undergo: 1. A standard of care 4DCT scan for radiation therapy simulation, 2. Pulmonary Function Tests (PFT) 3. A 4D attenuation correction CT 4. Breath Hold Computed Tomography (BHCT) imaging where static end-inspiration and end-expiration BHCT scans will be acquired, 5. Nuclear medicine imaging where a Tc-99m MAA SPECT perfusion scan and a Galligas PET ventilation scan will be acquired, 6. Fluoroscopy where 1-breath cine-fluoroscope sequences will be acquired at five different angles across the chest, 7. A 4D Cone Beam Computed Tomography (4DCBCT) scan. 8. Scans in points 4 to 7 above will be repeated at the end of treatment. Individual participants provide their own internal control. Galligas PET ventilation images (control) are compared with ventilation images derived from additional scans (comparator) for each participant. Tc-99m MAA SPECT perfusion images (control) are compared with perfusion images derived from BHCT scans (comparator) for each patient. There will be no change to patient treatment and patients will be treated using a standard of care anatomical based treatment plan. The pre-treatment 4DCBCT scan is part of standard of care.
Status | Not yet recruiting |
Enrollment | 15 |
Est. completion date | September 1, 2026 |
Est. primary completion date | September 1, 2026 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - Aged 18 years or older. - Eastern Cooperative Oncology Group (ECOG) performance status 0-2. - Histologically proven Stage II-IV non-small cell lung cancer as determined using the IASLC International Association for the Study of Lung Cancer (IASLC) 8th edition lung cancer staging guidelines. - To be treated with curative intent (stage II-III) or palliative intent (stage IV) with non-SABR external beam radiotherapy (e.g. 60 Gy in 30 treatments for curative intent or 30 Gy in 5 treatments for palliative intent). - Pulmonary function tests within 8 weeks of registration. - 4DCT simulation for radiation therapy. - Willingness to give written informed consent. - Willingness and ability to comply with the study procedures and visit requirements. - Available for follow up for 1 year or until death, whichever occurs first. Exclusion Criteria: - Prior radiation therapy to the thorax. - Prior surgery for this cancer. - Prior chemotherapy for this cancer. - Interstitial lung disease. - Pregnant women. |
Country | Name | City | State |
---|---|---|---|
Australia | Royal North Shore Hospital | St Leonards | New South Wales |
Lead Sponsor | Collaborator |
---|---|
University of Sydney | National Health and Medical Research Council, Australia, Northern Sydney and Central Coast Area Health Service |
Australia,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Physiological accuracy of X-ray-based ventilation imaging (BHCT, fluoroscopy, 4DCBCT, 4DCT) | Voxel-based Spearman correlation between X-ray-based ventilation imaging and nuclear medicine ventilation images (Galligas PET) | 1 week | |
Secondary | Difference in mean dose to high functioning lung structures between avoidance treatment plans and standard of care anatomical based treatment plans. | Difference in mean dose delivered to high functioning lung structures | 1 week | |
Secondary | Difference in percentage volume of high functioning lung structures receiving 20 Gray (20Gy) or more between functional lung avoidance treatment plans and standard of care anatomical based treatment plans. | Difference in percentage volume of high functioning lung structures receiving 20Gy or more. | 1 week | |
Secondary | Reduction in predicted risk of grade 2+ radiation pneumonitis (CTCAE v5) in functional lung avoidance treatment plans compared to standard of care anatomical based treatment plans. | Reduction in grade 2+ radiation pneumonitis rates quantified using Normal Tissue Complication Probability (NTCP) models. | 1 week | |
Secondary | Increased burden in the radiotherapy workflow involved with creating functional lung avoidance treatment plans. | Time required to conduct the additional imaging, produce the ventilation image, and creating the functional treatment plan. | 2 weeks | |
Secondary | Change in ventilation from lung radiation therapy. | Voxel-based Spearman correlation. Pre- and post-treatment X-ray-based ventilation images will be compared to pre- and post-treatment Galligas PET ventilation scans. | 8 weeks | |
Secondary | Physiological accuracy of CT perfusion imaging | Voxel-based Spearman correlation between CT perfusion imaging and nuclear medicine perfusion images (Tc-99m MAA) | 1 week | |
Secondary | Improvement in 4D PET image reconstruction using 4D attenuation CT | Quantification of PET signal within the lung | 1 week |
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