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Recruiting NCT06967961

NCT06967961 Research of Double-positive Circulating Cells (Tumor Marker / CD45+) in Several Types of Metastatic Cancers

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Clinical Trial Summary
NCT ID NCT06967961
Status Recruiting
Phase
Sponsor Institut Claudius Regaud
Condition Urothelial Carcinoma
Study Type INTERVENTIONAL
Enrollment 450 participants
Start Date 2025-07-23
Primary Completion 2029-07-23

Trial Parameters

Condition Urothelial Carcinoma
Sponsor Institut Claudius Regaud
Study Type INTERVENTIONAL
Phase N/A
Enrollment 450
Sex ALL
Min Age 18 Years
Max Age N/A
Start Date 2025-07-23
Completion 2029-07-23
Interventions
For each enrolled patient, the sample described below will be collected as specific intervention intended for research purposes:

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Brief 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 Criteria

Inclusion Criteria: * 1\. 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 * 2\. Metastatic disease for which the treatment (whatever the line) has not been initiated yet * 3\. Age ≥ 18 years * 4\. Patient affiliated to a French Social Security scheme * 5\. Patient having signed his/her informed consent prior to inclusion in the study and prior to any specific procedure for the study. Exclusion Criteria: * 1\. Patient with localized disease. * 2\. Pregnant or breast-feeding women. * 3\. Any psychological, family, geographical or sociological condition that prevents compliance with the medical monitoring and/or procedures set out in the study protocol. * 4\. Patient who has forfeited his/her freedom by administrative or legal award or who is under

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