Circulating Tumor DNA Guided Treatment Monitoring in Advanced Lung Cancer
NCT05889247
Summary
The study is a prospective randomized interventional study including patients with advanced non-small cell lung cancer, receiving immunotherapy, with the aim of optimizing treatment monitoring. The study aims to investigate the clinical utility of liquid biopsy monitoring in order to reduce the numbers of inefficient treatments and needless toxicity - and to explore the cost-effectiveness and cost-utility of introducing liquid biopsy monitoring in daily clinical practice.
Eligibility
Inclusion Criteria: * Newly diagnosed, histologically verified, Non-Small Cell Lung Cancer (NSCLC) * Advanced or locally advanced disease without curative intended treatment options * Age \> 18 years * Eastern Cooperative Oncology Group (ECOG) score of Performance Status (PS) 0-1 * Measurable disease according to the iRECIST criteria version 1.1. * Eligible to first line immunotherapy (monotherapy) * Signed informed consent Exclusion Criteria: * Targetable alterations in EGFR, ALK or ROS-1 * Other active cancers
Conditions3
Browse More Trials
Trial data from ClinicalTrials.gov. Trial status and eligibility can change — verify directly with the study contact or on ClinicalTrials.gov.
This site does not provide medical advice. Always consult your doctor before considering enrollment in a clinical trial. Learn more on our About page.
NCT05889247