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Recruiting NCT07820566

Development of a Preclinical 3D Vascularized and Perfused Tumoroid Model in Oncology and Urology Developed From Patient Tumors (Kidney, Bladder, and Prostate Cancers)

Conditions: Kidney Cancers, Bladder Cancer, Prostate Cancer

Sex: All
Ages: 18 Years – N/A
Enrollment: 100
Sponsor: University Hospital, Strasbourg, France

Location: Service de Chirurgie Urologique _ Hôpitaux Universitaires de Strasbourg Strasbourg

Summary

This is a study : * Single-center * Prospective * Translational * Based on data and blood samples. In this context, the aim is to collect approximately 10 ml of blood from each patient included in the 3D tumoroid development project. The main objective is to establish and validate a panel of vascularized and perfused 3D tumoroids for personalized medicine based on patient tumors for urological cancers, incorporating autologous immune cells. Translated with DeepL.com (free version)

Eligibility Criteria

Inclusion Criteria: Inclusion criteria: * Criteria common to all patients: * Male or female subject (≥18 years old); * Diagnosed with kidney cancer, prostate cancer, or bladder cancer; * whose tumor tissue and associated data are reused as part of the SphéroUro protocol (study outside the Jardé law, retrospective study on tumor tissue and associated data, from the biobank registered with the Ministry of Education and Research under reference No. DC 2016-2677); * affiliated with a social security health insurance scheme or beneficiary of such a scheme; * agreeing to participate in the 3DBlood study. * Specific criteria for patients with renal cell carcinoma (RCC): * Extended nephrectomy (EN) (larger tumor, closer to the sinus; therefore at greater risk of metastasis): with a cavo, cavectomy (neoplastic thrombus in the vena cava), or renal vein bud, or lymph node dissection, or with adrenalectomy (often for tumors, therefore possible metastases). Or \- Partial nephrectomy (PN): with tumors at stage T2 or T3a) Exclusion Criteria: * Patient refusal to participate in the study; * Inability to provide the subject with informed consent (subject in an emergency situation, difficulties in understanding the subject, etc.); * Patient under legal protection, guardianship, or conservatorship; * Patient currently participating in a therapeutic clinical trial (i.e., gene therapy or other).

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View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT07820566). StuddyBuddy aggregates publicly available trial information.