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Implementation of Up-front ctDNA Into Lung Cancer Care and Development of Liquid Biopsy-based Decision Support Models - LM² Study

Recruitingn/aAges 18 Years - anyAllCatharina Ziekenhuis Eindhoven
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In plain words

What the trial is, and whether it could suit you

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 the

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📋 Eligibility rules (as published)
Inclusion Criteria: * Aged 18 or above and suspected of having lung cancer Exclusion Criteria: * Presence of another malignant tumor, i.e. diagnosed with a tumor in the past 5 years
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What it tests

  • Not listed
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Where

5 sites
Zuyderland Medical Center
Heerlen, Netherlands
Maastricht University Medical Center
Maastricht, Netherlands
Catharina Ziekenhuis Eindhoven
Eindhoven, Netherlands
St. Anna Ziekenhuis
Geldrop, Netherlands
Máxima Medisch Centrum
Veldhoven, Netherlands
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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