Research of Double-positive Circulating Cells (Tumor Marker / CD45+) in Several Types of Metastatic Cancers
Institut Claudius Regaud
450 participants
Jul 23, 2025
INTERVENTIONAL
Conditions
Summary
A prospective, proof-of-concept pilot study in patients with metastatic cancers (9 types of cancers are studied) treated at the IUCT-O or possibly in other institutions. Eligible patients will be selected and informed of this study during a medical consultation for their cancer by medical oncologists. Then, with the patient's consent and before the start of anti-cancer treatment (whatever the line), a blood sample will be taken to detect DP-circulating cells by 2 different methods of analysis. Each patient will participate in the study for one day. The methods of analysis will be: flow cytometry for all patients and either Parsotix® or CellSearch® depending on the type of cancer. 450 patients will be enrolled in total.
Eligibility
Inclusion Criteria5
- \. Patients with one of the following cancer types: urothelial carcinoma, renal carcinoma, prostate adenocarcinoma, upper aerodigestive tract carcinoma, cervival carcinoma, adenocarcinoma of endometrium, cutaneous melanoma, soft tissue sarcoma, seminomatous and nonseminomatous germ cell tumors
- \. Metastatic disease for which the treatment (whatever the line) has not been initiated yet
- \. Age ≥ 18 years
- \. Patient affiliated to a French Social Security scheme
- \. Patient having signed his/her informed consent prior to inclusion in the study and prior to any specific procedure for the study.
Exclusion Criteria4
- \. Patient with localized disease.
- \. Pregnant or breast-feeding women.
- \. Any psychological, family, geographical or sociological condition that prevents compliance with the medical monitoring and/or procedures set out in the study protocol.
- \. Patient who has forfeited his/her freedom by administrative or legal award or who is under legal protection (curatorship and guardianship, protection of justice).
Interventions
A blood sample will be taken before initiation of the metastatic treatment line and will be analyzed by 2 distinct methods. The total blood volume withdrawn per patient is approximately 30mL.
Locations(1)
View Full Details on ClinicalTrials.gov
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NCT06967961