跳至主要内容
临床试验/NCT06666803
NCT06666803招募中不适用

Functional, Personalised and Integrated Profiling of Biopsied Pancreatic Tumours

IHU Strasbourg3 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2025年1月27日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
60
试验地点
3
主要终点
Organoid culture from PDAC EUS-FNB biopsy

研究概览

简要总结

Pancreatic ductal adenocarcinoma (PDAC) has the poorest prognosis of all digestive cancers due to lack of early diagnosis and limited response to treatment. Patient-derived organoid technology has become a mainstay of precision oncology, enabling personalised functional characterisation of tumours (e.g. treatment evaluation and drug screening). Initial research carried out as part of the Cancer Profile project has produced the first organoids from resected PDAC parts.

Only 15-20% of patients can benefit from surgical resection, which remains the only curative treatment. In contrast, most patients with PDAC undergo diagnostic fine-needle biopsies (FNB) using an echo-endoscopic procedure (EUS). The next step is therefore the reliable generation of organoids from limited quantities of biopsy material obtained by 'EUS-FNB'.

The aim of the study presented here is to validate these organoids on the basis of the following characteristics: (i) morphological and proliferative characteristics, (ii) recapitulation of the genetic characteristics of the original tumour, (iii) expression of tumour markers.

详细描述

Pancreatic Ductal AdenoCarcinoma (PDAC) has the poorest prognosis of all digestive cancers due to lack of early diagnosis and limited response to treatment. Its mortality rate is expected to increase in Western countries as populations age and obesity levels rise. Its diagnosis is generally made late in the course of the disease and only 15-20% of patients can benefit from surgical resection, which remains the only curative treatment. Thus, palliative chemotherapy remains a mainstay of the management of this disease. Despite the new approach to treating advanced cancers using molecular characterisation of tumour tissue, only a small subset of patients has access to this personalised treatment and around 13% of patients show a significant response.

Patient-derived organoid (PDO) technology enables personalised functional characterisation of tumours (e.g. treatment evaluation and drug screening).

PDO are created from adult tumour-derived stem cells and self-organise into structures similar to the corresponding tissue architecture in vivo. In pancreatic cancer, PDO have recapitulated the histology and genetic alterations of the original tumour and have been proved reliable in predicting sensitivities to a range of therapeutic compounds. While the majority of PDAC organoids described have been created from surgical resections, only a few examples of PDAC organoids successfully generated from biopsies have been reported.

Given that most PDAC patients are not eligible for surgical resection and therefore undergo diagnostic fine-needle biopsies (FNB) by endoscopic ultrasound (EUS) (EUS-FNB), efforts are needed to improve the generation of PDAC organoids from limited quantities of material. This will ensure that as many PDAC patients as possible can benefit from large-scale drug screening, a technic able to validate gene-drug associations, guide treatment decision-making and known to be well-suited to PDO.

The Cancer Profile project is a European collaboration between the IHU Strasbourg and the LIH, funded respectively by the ANR (Agence Nationale de la Recherche, France) and the FNR (Fonds National de la Recherche, Luxembourg). Its ultimate aim is to be able to profile each tumour sample accurately, in an automated and personalised way. A first trial has enabled the establishment of the technique and conditions for culturing spheroids of pancreatic origin.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Basic Science
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Adult patient over 18 years of age.
  • Patient undergoing echo-endoscopy with certainty/suspicion of fine needle biopsy (EUS-FNB).
  • Suspicion of pancreatic lesion
  • Patient able to receive and understand information relating to the research protocol and to give consent.
  • Patient affiliated to the French social security system.

排除标准

  • Patient not programmed for endoscopy with certainty/suspicion of fine needle biopsy (EUS-FNB).
  • Patient undergoing echo-endoscopy and presenting a high risk that may prevent EUS-FNB.
  • Patient with degenerated Intraductal papillary mucinous neoplasm (IPMN)
  • Patient with acute pancreatitis within 4 weeks prior to EUS
  • Pregnant or breast-feeding patient
  • Patient under court protection.
  • Patient under guardianship or curatorship.
  • Patient in a situation of social vulnerability.
  • Patient under legal protection or unable to express his/her opposition.

研究组 & 干预措施

FNB and blood sample analysis

Experimental

干预措施: FNB sampling (Other)

FNB and blood sample analysis

Experimental

干预措施: blood sampling (Biological)

结局指标

主要结局

Organoid culture from PDAC EUS-FNB biopsy

时间窗: 8 weeks

Qualitative assessment in the obtention of organoids. The main objective will be validated when a culture of functional organoids is generated.

次要结局

  • Assessment of the overall accuracy of characterising PDAC EUS-FNB samples by optical slicing based on dynamic full-field optical coherence tomography (D-FF-OCT)(Day 1)
  • Evaluation of the protocol for culturing organoids derived from PDAC EUS-FNB biopsies.(3 months)

研究者

发起方
IHU Strasbourg
申办方类型
Other
责任方
Sponsor

研究点 (3)

Loading locations...

相似试验

Functional, Personalised and Integrated Profiling of... | 临床试验