Non Small Cell Lung Cancer
Conditions
Brief summary
This is a prospective observational pilot study to investigate levels of circulating tumour DNA (ctDNA) in plasma from patients with stage I to IIIB non-small cell lung cancer (NSCLC) who will undergo treatment with curative intent.
Detailed description
Taking as reference tumour-specific somatic genetic alterations identified within individual cancer biopsies from patients, recent advances in genomic and next generation sequencing technologies now provide the opportunity to investigate whether each patient's tumour-specific DNA can be reliably detected within their plasma. This offers the possibility to test a patient's response following treatment with curative intent. This technology has already been used to detect ctDNA in metastatic NSCLC, but not yet in early stage disease. The primary objective of this pilot study is to test the feasibility of detecting serial ctDNA levels in stage I to IIIB NSCLC patients who undergo treatment with curative intent. As secondary endpoints, this study aims to measure ctDNA levels and characteristics, and to correlate them with clinical features (such as burden of disease and treatment response) in order to test the value of ctDNA as a diagnostic, prognostic and predictive biomarker for patients with NSCLC. 100 patients planned for curative treatment (surgery or radical radiotherapy +/- chemotherapy) will be recruited.
Interventions
PROCEDUREBlood sampling
Blood samples will be obtained during routine clinical visits. Ideally, two 9mL blood samples (or equivalent volume) will be collected into EDTA or other appropriate blood collection tube at each time point except at baseline, where three EDTA 9mL tubes and one of 2.6mL (for study of whole blood) will be collected.
PROCEDURESurplus Tumour Tissue sample collection from surgery
In surgical patients, lung tumour samples and normal lung tissue will be obtained from surplus tissue removed at the time of surgery. No extra procedures (biopsies or surgeries) are requested for the study.
OTHERCollection or archival tumour tissue (If available)
Where available surplus tumour and normal tissue from archival tissue will be collected for analysis.
Sponsors
Cambridge University Hospitals NHS Foundation Trust
University of Cambridge
CCTU- Cancer Theme
Study design
Observational model
OTHER
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Age ≥ 18 years old at the time of consent * Male or Female * Patients with radiologically and histologically/cytologically confirmed stages I to IIIB NSCLC who are planning to undergo radical treatment (surgery or radical radiotherapy) with curative intent * ECOG Performance Status 0-2 * Able to give informed consent * Able to give blood
Exclusion criteria
* Unable to receive treatment with curative intent due to co-morbidity or personal choice Patients participating in other clinical studies are not precluded from entering the study; however they must meet all the eligibility criteria for this study.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| ctDNA detection rate in all patients | Baseline blood sample | The primary endpoint is the ctDNA detection rate in the baseline blood sample of early stage NSCLC patients undergoing treatment with curative intent. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| ctDNA levels, genetic alterations and other characteristics with clinical features in all patients | Blood samples will be taken at routine clinic visits through study completion, an average of 3 years. | To correlate ctDNA levels (fraction and/or absolute amplifiable copies), genetic alterations and other ctDNA characteristics with clinical features such as response to treatment, burden of disease (as evaluated by, e.g. radiology, pathology or performance status), disease relapse and future outcomes. |
| Comparison of ctDNA levels and mutation profile at relapse to that obtained at earlier time points | Blood samples will be taken at relapse through study completion, an average of 3 years. | To compare the ctDNA levels and mutation profile at relapse to that obtained at earlier time points |
| ctDNA baseline levels, genetic alterations and other features in all patients | Baseline blood sample | To quantify the baseline levels, genetic alterations and other features of ctDNA in patients with NSCLC undergoing treatment with curative intent |
| Test ctDNA levels, genetic alterations or other characteristics during and after treatment with radical radiotherapy | Blood samples will be taken every week of radiotherapy and at follow-up clinic visits, approximately every 3 months for 9 months after the end of treatment | To test ctDNA levels, genetic alterations or other characteristics, before, during and after treatment with radical radiotherapy (with or without chemotherapy) and to correlate them with clinical features, e.g. response to treatment and clinical outcomes |
| Establish a library of samples for future analysis | Blood samples will be taken at baseline, during treatment and at follow-up clinic visits, approximately every 3 months for 9 months after treatment | To establish a library of samples for future analysis using more advanced technology, i.e. to achieve a more detailed retrospective analysis of ctDNA levels and genomic alterations/features in relation to clinical outcomes. |
| Correlate the genetic alterations found in different regions of each tumour with histological features and genetic alterations in the ctDNA | Lung tumour tissue will be collected from surgery through end of study, an average of 3 years. | To correlate the genetic alterations found in different regions of each tumour with histological features and genetic alterations in the ctDNA |
Countries
United Kingdom
Contacts
Primary ContactCambridge Clinical Trials Unit - Cancer Theme
Outcome results
None listed