Clinical Trials Directory

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

TypeNameDescription
OTHERCirculating 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.