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CIRculating CANcer MAster-Protocol

MAster Protocol Studying the Impact of Blood Biopsy on Screening, Diagnosis, Diagnostic and Follow-up of Solid Cancer in Adult

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05089747
Acronym
CIRCAN MAP
Enrollment
6000
Registered
2021-10-22
Start date
2022-12-05
Completion date
2047-12-01
Last updated
2026-06-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Adult With Solid Cancer

Keywords

liquid biopsy, solid cancer

Brief summary

This exploratory study will focus on the development of the analyses of blood biomarkers to better understand the circulating biomarkers associated with cancer diagnosis, treatment efficacy and progressive disease

Interventions

BIOLOGICALBlood 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).

Sponsors

Hospices Civils de Lyon
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Adult (\>18y) * 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

* Refusal to participate * 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

Design outcomes

Primary

MeasureTime frameDescription
Liquid biopsy analysesDay 0Extraction of circulating DNA or circulating RNA followed by a tumoral cells extraction.
Standard technics of disease assessmentWeek 16Genetic and transcriptomic explorations with immunofluorescence technique. Marking with specific markers of the tumor pathology. And enumaration of tumoral cells.
Correlation between outcome 1 and outcome 2year 5Building a biological collection of blood samples and following, diagnosis and prediction of adult solid cancer.

Countries

France

Contacts

CONTACTSebastian Couraud, MD, PhD
sebastien.couraud@chu-lyon.fr+33 4 478 864 401

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 11, 2026