Development of a Preclinical 3D Vascularized and Perfused Tumoroid Model in Oncology and Urology Developed From Patient Tumors (Kidney, Bladder, and Prostate Cancers) (3DBlood)
2026年9月9日 更新者:University Hospital, Strasbourg, France
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)
研究概览
研究类型
观察性的
注册 (估计的)
100
联系人和位置
本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。
学习联系方式
- 姓名:Hervé LANG, PUPH
- 电话号码:33369550974
- 邮箱:Herve.Lang@chru-strasbourg.fr
学习地点
-
-
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Strasbourg、法国、67091
- 招聘中
- Service de Chirurgie Urologique _ Hôpitaux Universitaires de Strasbourg
-
接触:
- Hervé LANG, PUPH
- 电话号码:33 3 69 55 09 74
- 邮箱:herve.lang@chru-strasbourg.fr
-
首席研究员:
- Hervé LANG, PUPH
-
副研究员:
- Nicolas MEYER, PUPH
-
-
参与标准
研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。
资格标准
适合学习的年龄
- 成人
- 年长者
接受健康志愿者
不适用
取样方法
非概率样本
研究人群
- 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)
描述
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).
学习计划
本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。
研究是如何设计的?
设计细节
研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Constitute and validate a panel of vascularized and perfused 3D tumoroids for personalized medicine based on patient tumors for urological cancers, incorporating autologous immune cells.
大体时间:Day 1 after surgery
|
For the establishment of the models, it is necessary to have: sufficient cell viability after enzymatic dissociation of the tissues and a correspondence of patient/model 3D therapeutic responses.
The patients' blood will be collected to isolate immune cells using a Ficoll gradient, to integrate them into the forming 3D structures, taking into account the proportion present in the primary tumor tissues of each patient, for the 3D structures developed from their tumor.
|
Day 1 after surgery
|
合作者和调查者
在这里您可以找到参与这项研究的人员和组织。
研究记录日期
这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。
研究主要日期
学习开始 (实际的)
2024年9月2日
初级完成 (估计的)
2029年9月1日
研究完成 (估计的)
2029年9月1日
研究注册日期
首次提交
2026年1月5日
首先提交符合 QC 标准的
2026年9月9日
首次发布 (实际的)
2026年9月15日
研究记录更新
最后更新发布 (实际的)
2026年9月15日
上次提交的符合 QC 标准的更新
2026年9月9日
最后验证
2026年1月1日
更多信息
此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.