Analysis of circulating tumor markers in blood in lung cancer patients
Official title: Analysis of Circulating Tumor Markers in Blood - ALCINA 5
Run by Institut du Cancer de Montpellier - Val d'Aurelle · NCT07060950 · Data updated 2026-11-12
This study tests whether blood-based tumor markers can help understand and monitor lung cancer in adults to complement tissue tests.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 620 (estimated) |
| Sponsor | Institut du Cancer de Montpellier - Val d'Aurelle Academic / other |
| Drugs / interventions | chemotherapy |
| Locations | 1 site (Montpellier, France) |
| Status | Recruiting |
| Started | September 26, 2025 |
| Main results expected | July 2030 |
| Study ends | July 2035 |
| Registry record updated | November 6, 2026 |
| Trial ID | NCT07060950 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults (18+) with an invasive tumor pathology eligible for biopsy and able to provide informed consent, including those with suspected or confirmed cancer suitable for blood biomarker analysis in France.
✕Probably not a fit
Patients whose tumor biology does not shed measurable circulating markers or who do not undergo interventions that affect marker dynamics may see limited benefit.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
ALCINA 5 is a small-cohort, interventional study that uses blood samples to analyze circulating tumor biomarkers in patients with invasive tumors, including non-small cell lung cancer. Researchers compare blood markers with tumor tissue when available and examine how marker levels change in relation to events like chemotherapy, biopsy, or surgery. The aim is to determine the feasibility and potential utility of liquid biopsy markers and their kinetics for clinical decision-making. If initial results are promising, further larger studies may be planned under applicable approvals. The study is conducted at a French cancer center with basic inclusion and exclusion criteria focusing on adults who can consent and are affiliated with the social protection system.
Why it matters
Potential benefit: If successful, patients could benefit from less invasive monitoring of their cancer through blood tests that reflect tumor biology and treatment response.
How similar studies have gone: Previous research shows promise for circulating tumor markers in guiding cancer management, but results vary and broader validation is needed.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: 1. Patient presenting an invasive tumoral pathology (proved or suspected), whatever is the location or the stage, 2. 18 years old or higher ? 3. Patient who has provided informed, written, and explicit consent, 4. Patient affiliated with a French Social Protection System. In the case of a tumor biopsy: 5. Tumor considered as accessible by biopsy, 6. Normal hemostasis assessment (PT, APTT, platelets), 7. No anticoagulant or antiaggregant treatment for the biopsy. Exclusion Criteria: 1. Pregnant woman and/or breast-feeding, 2. Patient whose regular follow-up is impossible for psychological, family, social or geographical reasons, 3. Private persons of freedom or under guardianship, 4. Patient with a history of other invasive cancers within the 5 years preceding inclusion.
Where it's running
-
Centre Regional de Lutte Contre le Cancer - Centre Val d'Aurelle
Montpellier, France, France Recruiting
Study contacts
- Study coordinator: Emmanuelle TEXIER
- Email: emmanuelle.texier@icm.unicancer.fr
- Phone: 467613102
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.