Non-small Cell Lung Cancer
Conditions
Brief summary
The trial evaluates the utility of 18FDG-PET/CT scan in the target definition process when SBRT is planned for stage I NSCLC.
Detailed description
The trial aims to evaluate the utility of 18FDG-PET/CT in SBRT planning for NSCLC with particular emphasis on the definition of macroscopic and microscopic boundaries of malignant growth. Studies indicate that the definition of the gross tumor volume may gain in quality when CT and 18FDG-PET are combined. In about 30-60% of NSCLC patients considered for radiotherapy, alteration of CT-based treatment volumes is the consequence of a supplementary 18FDG-PET scan. Studies examining the effect of combined PET/CT scans on the delineation of the GTV generally show reduced intra- and inter-clinician variability. Whether this higher degree of consistency is an actual improvement remains to be proven. Pathological specimens from operated NSCLC patients may serve as a gold standard in this respect. To meet the need for tight margins, the clinical target volume in SBRT planning is generally presumed to correspond to the GTV. Whether this clinical practice rests on firm ground is also an issue that can be addressed in a PET-CT-pathology correlation study.
Interventions
PROCEDUREPET/CT scan
Sponsors
The Danish Medical Research Council
University of Aarhus
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Age 18 years or above * Histologically or cytologically verified NSCLC * Disease stage I (T1-2 N0 M0) * Referred from the multi-disciplinary lung cancer conference at Aarhus University Hospital for operation at Skejby Hospital, Aarhus University Hospital * Oral and written informed consent
Exclusion criteria
* Medically treated diabetes mellitus * Fasting blood-glucoses above 6,7 mM * Blood-creatinin above normal * Allergies to intravenous contrast * Detention according to the Danish laws on psychiatrics that does not comply with participation in a clinical trial * Employment at the Dept. of Oncology, Aarhus University Hospital * Pregnancy * Lactation
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Concordance indices between CT-based and PET/CT-based target definitions versus volumes of surgical specimens | 1 month |
Secondary
| Measure | Time frame |
|---|---|
| Intra- and inter-individual variability of target definition | 1 month |
Outcome results
None listed