Clinical trial Recruiting at 2 sites Interventional Ages 18 and up

Analysis of blood biomarkers in cancer patients

Official title: Analysis of Circulating Tumor mArkers in Blood 4 - ALCINA 4

Run by Institut Curie · NCT05088395 · Data updated 2026-11-12

This study is testing how blood samples from cancer patients can help doctors better understand and treat their cancer.

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Quick facts

Study typeInterventional
Ages18 Years and up
SexAll
Enrollment2050 (estimated)
SponsorInstitut Curie
Academic / other
Locations2 sites (Paris and 1 other locations)
StatusRecruiting
StartedMay 19, 2022
Main results expectedJune 1, 2031
Study endsJune 1, 2031
Registry record updatedApril 14, 2026
Trial IDNCT05088395 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates for this study are adult cancer patients who are being treated at one of the participating centers.

Probably not a fit

Patients who are pregnant or breastfeeding may not benefit from this study due to specific cohort requirements.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

The ALCINA 4 study is a prospective biological cohort study that focuses on analyzing circulating tumor biomarkers obtained through blood sampling from cancer patients. Participants will provide up to four blood samples over a period of 12 to 18 months, with the timing varying based on the specific cohort and clinical context. The study aims to explore various biomarkers, including circulating tumor cells and circulating tumor DNA, to enhance cancer diagnosis, prognosis, and treatment efficacy. Additionally, it may involve tumor biopsies if necessary for comparison with blood samples.

Why it matters

Potential benefit: If successful, this study could lead to improved diagnostic and treatment strategies for cancer patients through the use of blood-based biomarkers.

How similar studies have gone: Other studies have shown promise in using circulating biomarkers for cancer diagnosis and treatment monitoring, indicating that this approach is gaining traction in the field.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Patient treated for cancer at one of the participating center
* 18 years old or higher
* Signed informed consent form
* Patient not deprived of their liberty or under guardianship (including temporary guardianship)
* Patient covered by social security scheme
* Patient with no compliance issue (related to geographical, social or psychological reasons) for study follow up
* Other additional criteria will be defined (defining tumor type and clinical setting), by cohort

If a biopsy tumor sample is to be taken:

* Tumor considered as accessible by biopsy (at the investigator's discretion).
* Normal blood coagulation tests (if applicable, and in case of a non-superficial tumor lesion).
* No anticoagulant or antiaggregant treatment for the biopsy.

Exclusion Criteria :

Pregnant and/or breast-feeding women depending on cohort.

Where it's running

  • Institut Curie
    Paris, France
    Recruiting
  • Institut Curie
    Saint-Cloud, France
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
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Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.