Non Small Cell Lung Cancer (NSCLC)
Conditions
Keywords
Stereotactive Body Radiation Therapy (SBRT), Lung Fibrosis, FLT-PET, NSCLC
Brief summary
Stereotactic body radiotherapy (SBRT) has emerged as one of the leading curative method for early stage non-small cell lung cancer (NSCLC). However, assessing the status of the disease during post-SBRT follow up presents a challenge. Currently, chest Computed Tomography (CT) is the main technique to detect whether cancer has come back, but this method has demonstrated poor accuracy and reliability in determining if the observed post-operative lung changes are benign or malignant. Positron-emission tomography (PET) is an imaging technique that uses special radioactive tracers to cell growth. The use of PET scans with a tracer that target the pathways of DNA synthesis may be more accurate than CT for detecting if the cancer has come or not. The purpose of this study is to see if a PET radiotracer called 18F-FLT (3'-deoxy-3'-fluorothymidine) can identify cancer recurrences accurately compared to regular CT scans.
Detailed description
Stereotactic body radiotherapy (SBRT) has demonstrated an impressive 3-year control rate of higher than 90% for early stage NSCLC, leading to increased use of this technique as a curative method for lung cancer treatment. With growing clinical experience with this technique, post-SBRT follow up has received more attention. Follow up after SBRT is done primarily by thorax CT, which is affected by radiation-induced radiographic lung changes that can resemble or obscure local recurrence. FLT (3'-deoxy-3'-fluorothymidine) is a thymidine analogue which is non-toxic in tracer doses, and can be labeled with 18F. FLT-PET is a type of imaging (similar concept to the widely used 18-FDG PET-CT) that is based on integration of thymidine into DNA for assessment of proliferation. Conceptually, increased DNA synthesis is correlated to tumor aggressiveness and response to therapy, more so than glucose utilization - as in FDG-PET could be. The purpose of this study is therefore to see what added information the use of FTL-PET can provide in distinguishing between changes in the lung that occur as a result of treatment that are not cancerous and those that are due to recurrence or progressive disease.
Interventions
PROCEDUREFLT-PET
Positron emission tomography scan using the 18f-FLT (3'deoxy-3'-fluorothymidine) tracer
Sponsors
University Health Network, Toronto
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
1. Age ≥ 18 years 2. Must have been treated at or plan to be treated at Princess Margaret Cancer Centre with SBRT for an early-stage NSCLC (T1N0M0; T2N0M0; or T3N0M0 chest wall primary tumours only) and are either: 1. Prior to treatment with lung SBRT (for Cohort 1) 2. Have radiographic findings on that are felt to be related to fibrosis at any time point following lung SBRT 3. Have radiographic findings on CT that are suspicious for recurrence at any time point following lung SBRT 3. Ability to provide written informed consent to participate in the study
Exclusion criteria
1. Previous systemic therapy 2. Previous thoracic radiotherapy(excluding the index lung SBRT treatment) 3. Active malignancy other than lung cancer 4. Unable to remain supine for more than 30 minutes 5. If taking the drug Antabuse 6. Pregnancy
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To report the SUVmax for the three cohorts | 1 year |
Secondary
| Measure | Time frame |
|---|---|
| To compare FLT uptake in 4D (respiratory sorted) versus free breathing FLT-PET scans | 1 year |
Countries
Canada
Outcome results
None listed