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NCT06127654

PHASE3

Ventilation Imaging to Improve the Quality of Life for Patients With Lung Cancer Treated With Radiation Therapy

Sponsor: University of Sydney

View on ClinicalTrials.gov

Summary

This research project is testing a new treatment planning method for patients with lung cancer who will be treated with radiation therapy. This new method is called Computed Tomography (CT) ventilation imaging. It aims to help protect the healthiest parts of patient's lungs from being injured by the radiation therapy. The investigators will determine whether healthy lung sparing can improve the quality of life in these patients.

Official title: VITaL: A Randomised Controlled Trial Investigating Ventilation Imaging to Improve the Quality of Life for Patients With Lung Cancer Treated With Radiation Therapy

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

165

Start Date

2025-05

Completion Date

2028-12

Last Updated

2025-04-04

Healthy Volunteers

Conditions

Lung Cancer

Interventions

DEVICE

Healthy lung sparing treatment plan

CT Ventilation imaging will be used to create a healthy lung sparing treatment plan for patients who will receive radiation therapy treatment for their lung cancer.

Inclusion Criteria 1. Aged 18 years or older. 2. Eastern Cooperative Oncology Group (ECOG) performance status 0-2. 3. Histologically proven non-small cell lung cancer. 4. Stage 3 as determined using the IASLC (International Association for the Study of Lung Cancer) 8th edition lung cancer staging guidelines. 5. To be treated with curative intent external beam radiotherapy (60 Gy in 30 treatments or 55 Gy in 20 treatments) +/- concurrent chemotherapy and adjuvant PD1/PD-L1 inhibitors. 6. Whole body Positron Emission Tomography (PET) scan within 8 weeks of registration. 7. Pulmonary function tests within 8 weeks of registration. 8. Willingness to give written informed consent. 9. Willingness to comply with the study procedures and visit requirements. 10. Available for follow up for a minimum of 12 months and up to 3 years. Post-inclusion criteria includes the results of a Quality of Life (QoL) assessment and treatment plan assessment, neither of which are known prior to consent. The post-inclusion criteria for the VITaL trial are: 1. Functional Assessment of Cancer Therapy - Lung (FACT-L) Trial Outcome Index (TOI) score of ≥5, the clinically meaningful difference 2. The standard treatment plan shows that at least 16% of volume of the lungs (minus the Gross Tumour Volume (GTV)) will receive more than 20 Gy. This criterion is based on the difference in pneumonitis risk between patients receiving below (\~8%) and above (\~34%) this threshold. The QoL assessment is unlikely to eliminate any patients but is included for patients where no clinically meaningful difference will be possible. The treatment plan assessment may exclude 20% of otherwise eligible patients. Exclusion Criteria: 1. Serious medical comorbidities that may contraindicate curative radiotherapy. 2. Inability to attend full course of radiotherapy or follow-up visits. 3. A current or former diagnosis of interstitial lung disease. 4. Prior history of lung cancer within 5 years. 5. Prior thoracic radiotherapy at any time. 6. Prior surgery for this cancer within a year. 7. Prior chemotherapy for this cancer. 8. Pregnant or lactating women.

Locations (1)

Liverpool Hospital

Liverpool, New South Wales, Australia