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NCT07289646RecruitingPhase 3

Functional Lung Avoidance Planning Guided by Lung Perfusion PET/CT Versus Anatomical Planning for Lung Stereotactic Body Radiotherapy

Source: ClinicalTrials.gov · Last updated 15 Oct 2026

Brief summary (registry, in English)

Stereotactic body radiotherapy (SBRT) has an increasing role in the treatment of both primary and secondary lung tumors. However, lung SBRT remains associated with significant radiation induced lung injury (RILI). Indeed, the reported incidence of symptomatic radiation induced lung injury (grade≥2) in the published literature is up to 20%. A current challenge of lung SBRT is therefore to better preserve lung function and to reduce pulmonary toxicity. During standard lung SBRT planning, dose constraints are defined on the anatomical lung volume. This planning considers the lung as functionally uniform and does not take into account the variability of regional lung function distribution. Functional lung avoidance is an emerging concept in lung radiotherapy (RT). The technique aims at personalizing RT treatment planning to individuals' lung functional distribution, by sparing functional pulmonary areas while prioritizing delivery of high doses to non-functional regions. 68Ga-MAA lung perfusion PET/CT is a novel imaging modality for regional lung function assessment. As compared with conventional lung scintigraphy, lung perfusion PET/CT is inherently a vastly superior technology for image acquisition (higher sensitivity and spatial resolution, greater access to respiratory gated acquisition). A more accurate lung functional mapping improves the possibility of functional lung avoidance planning for SBRT. The hypothesis is that functional lung avoidance planning guided by 68Ga-MAA perfusion PET/CT, while delivering an optimal dose to the tumor, will reduce the frequency of RILI in patients treated with lung SBRT.

Status (registry)
Recruiting
Phase (registry)
Phase 3
Study type
Interventional
Enrollment
418 (estimated)
First submitted
2 Dec 2025
Start date
4 Sept 2026
Primary completion date
31 Jan 2030
Lead sponsor
University Hospital, Brest
Diseases
Lung cancer
NCT number
NCT07289646

What you commit to

  • Study type: Interventional · Phase 3
  • Planned participants: 418
  • From 4 Sept 2026 to the primary completion date, 31 Jan 2030
  • 2 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other

  • Inability to give informed consent
  • Patientsunder guardianship or curatorship
  • Pregnant or breastfeeding women.
  • Contraindications to the radiolabeled product infused for lung perfusion PET/CT.

Who the study is looking for

  • Patients aged \> 18 years planned to be treated in the radiotherapy department of the participating centers with SBRT for primary or secondary lung tumors will be eligible to participate into the study

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (2)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Chu Brest
Coordinator of this site? Confirm its status
BrestFranceRecruiting
Centre de Lutte Contre le Cancer Leon Bérard Lyon
Coordinator of this site? Confirm its status
LyonFranceNot yet recruiting

This page is information, not medical advice. Discuss any trial with your doctor.