Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
6000 participants
OBSERVATIONAL
2022-12-05
2047-12-01
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Adult with solid cancer. No intervention.
Blood sampling for biomarker analysis (microRNA, circulating DNA…)
From one to four blood samplings: at diagnosis, after the first cycle of treatment, end of treatment, progressive disease (or end of study).
Interventions
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Blood sampling for biomarker analysis (microRNA, circulating DNA…)
From one to four blood samplings: at diagnosis, after the first cycle of treatment, end of treatment, progressive disease (or end of study).
Eligibility Criteria
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Inclusion Criteria
* Owing a social security insurance
* Any solid cancer diagnosed by histopathology or cytology
* Patient with blood sampling required as per standard of care
* Informed consent signed
Exclusion Criteria
* No blood sampling required as per standard of care
* Hemoglobin \< 7g/dl (\< 9g/dl if respiratory or cardiovascular disease history)
* Heterologous blood transfusion in the last 48 hours
* Weight under 20 kg
18 Years
ALL
No
Sponsors
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Hospices Civils de Lyon
OTHER
Responsible Party
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Locations
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Service de Pneumologie Hôpital Louis Pradel / Groupement Hospitalier Est
Bron, , France
Service de Pneumologie Hôpital Croix-Rousse / Groupement Hospitalier Nord
Lyon, , France
Service de Pneumologie Aigue Spécialisée et Cancérologie Thoracique Hôpital Lyon-Sud / Groupement Hospitalier Sud
Pierre-Bénite, , France
Oncologie médicale Hôpital Lyon-Sud / Groupement Hospitalier Sud
Pierre-Bénite, , France
Service de dermatologie Hôpital Lyon-Sud / Groupement Hospitalier Sud
Pierre-Bénite, , France
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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69HCL21_0918
Identifier Type: -
Identifier Source: org_study_id
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