Trials / Completed
CompletedNCT03986463
CIrculating Tumour DNA in Lung Cancer (CITaDeL): Optimizing Sensitivity and Clinical Utility
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 40 (actual)
- Sponsor
- London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
This is a prospective observation study in patients with non-small cell lung cancer (NSCLC) starting either cytotoxic chemotherapy or radiation therapy. It will assess changes in circulating tumor DNA (ctDNA) in the days following the initiation of treatment, as well as longitudinal monitoring, to assess the dynamics and value of ctDNA in stage III-IV NSCLC.
Detailed description
The study consists of three cohorts of patients initiating a new treatment for their NSCLC. The cohorts of (1) patients starting concurrent chemotherapy and radiation for stage III NSCLC (2) patients with advanced NSCLC starting cytotoxic chemotherapy (with or without pembrolizumab) (3) patients with advanced NSCLC starting palliative radiation therapy. This study aims to study the changes in ctDNA levels following a new treatment in lung cancer patients and to explore if the diagnostic utility of ctDNA testing is improved immediately following treatment when tumour cells are actively dying. It will also examine the changes in ctDNA levels and mutational analysis longitudinally.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| OTHER | Circulating tumour DNA (ctDNA) | Circulating tumour DNA (ctDNA) will be isolated from blood samples |
Timeline
- Start date
- 2019-05-01
- Primary completion
- 2020-12-31
- Completion
- 2020-12-31
- First posted
- 2019-06-14
- Last updated
- 2021-02-18
Locations
1 site across 1 country: Canada
Source: ClinicalTrials.gov record NCT03986463. Inclusion in this directory is not an endorsement.