About this trial
Despite scientific evidence, use of liquid biopsy (LB) in diagnosis and monitoring of lung cancer (LC) is limited since it requires major changes in diagnostic and care pathways. Analyzing tumor markers (TMs), circulating tumor cells (CTCs) and circulating tumor DNA (ctDNA) in blood (LB) can inform about the nature of the tumor, the most appropriate therapy, therapy response and resistance.
Lungmarker2 is a multicenter, prospective, implementation and diagnostic cohort study. This study aims to implement up-front ctDNA analysis ('plasma first approach') into routine diagnostic work-up of all advanced stage LC patients in the Southeast of the Netherlands (the participating hospitals in the OncoZON region). Thereby, additional information about the molecular make-up of the tumor becomes available, the number of tissue Next-Generation Sequencing (NGS) analyses will decrease and time to therapeutic decision making is shortened. Next, using ctDNA, TM and other information, multi-parametric decision support models are built and validated that may support diagnosis, predict the outcome of the next imaging procedure and progression-free survival during follow-up. The final goal is to develop a super-resolution microscopy test that can detect PD-L1 expression on CTCs.
Eligibility criteria
Qualifiers
Aged 18 or above and suspected of having lung cancer
Disqualifiers
Presence of another malignant tumor, i.e. diagnosed with a tumor in the past 5 years
Trial design
Treatments tested in this trial
- Not listed
Trial groups
Sponsors and collaborators
Catharina Ziekenhuis Eindhoven
Lead sponsor
Eindhoven University of Technology
Collaborator
Roche BV Netherlands
Collaborator
Maxima Medical Center
Collaborator
Zuyderland Medisch Centrum
Collaborator
Maastricht University Medical Center
Collaborator
St. Anna Ziekenhuis, Geldrop, Netherlands
Collaborator
The Netherlands Cancer Institute
Collaborator