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NCT02866149 Clinical Trial

Analysis of Circulating Tumor Markers in the Blood (ALCINA)

Cancer Clinical Trial

— ALCINA  

Official title:
Analysis of Circulating Tumor Markers in the Blood

Clinical Trial Details — Status: Active, not recruiting

Administrative data
NCT number NCT02866149
Other study ID # IC 2015-02
Secondary ID
Status Active, not recruiting
Phase N/A
First received
Last updated
Start date July 2015
Est. completion date September 2025

Study information
Verified date September 2023
Source Institut Curie
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Exploratory study on blood-borne biological markers and their correlation with clinical and pathological characteristics.

Description:

Exploratory multi-cohort study including different types of cancer (different organs and/or different histological types). Each kind of blood-borne biological markers analyses corresponds to a cohort.

Recruitment information / eligibility
Status Active, not recruiting
Enrollment 682
Est. completion date September 2025
Est. primary completion date September 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: 1. Patient with any tumoral disease (proven or suspected), of any type and stage 2. More than18 years old 3. Signed informed consent form Additional inclusion criteria if a tumor sample is needed: 4. Tumor considered as accessible by biopsy 5. Normal blood coagulation tests on the last blood analysis Non-inclusion Criteria: 1. Patient in detention or protected by the law 2. Patient who cannot comply with the study follow up for geographical, social or psychological reasons Additional non-inclusion criteria if a tumor sample is needed: 3. Anticoagulant or antiaggregant that cannot be interrupted for the biopsy 4. central-nervous system metastases only (unless a diagnostic or curative surgery is planned before the inclusion in the study)

Study Design

Related Conditions & MeSH terms

Intervention

Biological:
• Blood sampling
Up to 5 blood samplings can be performed at different time points
Procedure:
• Tumor sampling
One tumor sampling can be performed, if applicable
Other:
• Stool sampling
Up to 5 blood samplings can be performed at different time points

Locations
Country Name City State
France Centre Georges François Leclerc Dijon
France Institut du Cancer de Montpellier Montpellier
France Institut Curie (Paris hospital) Paris
France Institut Mutualiste Montsouris Paris
France Institut Curie (St Cloud hospital) Saint-cloud

Sponsors (1)
Lead Sponsor Collaborator
Institut Curie

Country where clinical trial is conducted

France, 

Outcome
Type Measure Description Time frame Safety issue
Primary Feasibility of the analysis of different blood-borne tumor biomarkers Success rate of the tested detection techniques. The success rate of a given detection technique is calculated by the ratio " detection success " / " number of screened patients ". 18 months
Secondary Correlation with biological and clinical data Number of biological analysis results correlated to clinical data. Establishment of a proof of concept 18 months
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