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PDAC - Pancreatic Ductal AdenocarcinomaNCT06666803

Functional, Personalised and Integrated Profiling of Biopsied Pancreatic Tumours (CancerProfile by FNB)

A study testing FNB sampling and blood sampling in people with PDAC - Pancreatic Ductal Adenocarcinoma, run by IHU Strasbourg at 2 sites in France.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

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. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
PDAC - Pancreatic Ductal Adenocarcinoma
What is being tested?
FNB sampling and blood sampling
Could I receive a placebo?
No, everyone receives an active treatment
How many people
60 participants
Where
2 sitesFrance
Study dates
27 Jan 2025to Feb 2027
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • 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.

Who cannot join

  • 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.
Show all 9Show fewer
  • Patient under guardianship or curatorship.
  • Patient in a situation of social vulnerability.
  • Patient under legal protection or unable to express his/her opposition.

Trial locations and contacts

2 sites in 1 country. Contact the study team or a site near you to ask about taking part.

France2 sites, 2 recruiting
  • Centre d'Endoscopie Digestive

    Strasbourg

    Irina TCHOUMAK, +33 3 88 75 53 54, irina.tchoumak@hotmail.com

    Recruiting
  • Department of hepato-gastroenterology

    Strasbourg

    Recruiting

Other trials in France

About this study

Official title: Functional, Personalised and Integrated Profiling of Biopsied Pancreatic Tumours

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.

Read the detailed description

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.

The study proposed here is the next step in this project: the reliable generation of organoids from limited quantities of biopsy material obtained by EUS-FNB. This routine procedure is mandatory in the PDAC standard care to obtain tumour tissue for minimally invasive diagnosis and preoperative procedures such as preoperative chemotherapy.

In this clinical study, one to two biopsies will be devoted to the usual analysis performed as part of the care, and a supplementary biopsy will be added for the protocol. This biopsy will be divided in three parts: (i) a sample will be send for organoid culture, (ii) a sample will be preserved in liquid nitrogen and analysed later to check whether the mutations observed in the organoid are indeed identical to those present in the initial tissue, (iii) and a third sample will be analysed by Dynamic Full-field Optical coherence tomography (D-FF-OCT), an innovative technique for imaging living tissue. A blood sample will also be withdrawn for genomic analysis.

Once the first organoids are obtained, they will be validated on the basis of the following characteristics: (i) morphological and proliferative characteristics, (ii) genetic characteristics, and (iii) expression of tumour markers.

Being tested
FNB sampling, blood sampling
Keywords
PDAC, EUS, FNB, PDO, organoid, OCT

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • FNB samplingOther

    A supplementary FNB will be performed during the EUS procedure. Sample will be processed to obtain organoids and assess their morphological, proliferative and genetics characteristics.

  • blood samplingBiological

    A blood withdrawal will be performed during the EUS procedure. Sample will be processed to assess organoids morphological, proliferative and genetics characteristics.

Study groups in NCT06666803
Study groupRoleWhat they receive
FNB and blood sample analysisExperimentalNot described
Receives: Other: FNB sampling; Biological: blood sampling

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Organoid culture from PDAC EUS-FNB biopsy

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

    Measured: 8 weeks

Secondary outcomes (3)
  1. Evaluation of the protocol for culturing organoids derived from PDAC EUS-FNB biopsies.

    Evaluation of the mutations found in the organoid from the EUS-FNB biopsies compared to those in the original sample preserved in liquid nitrogen (qualitative criterion).

    Measured: 3 months

  2. Evaluation of the protocol for culturing organoids derived from PDAC EUS-FNB biopsies.

    Evaluation of the mutations observed in the cancerous tissue (snap-frozen sample) compared to those observed in the blood sample from the same patient.

    Measured: 3 months

  3. 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)

    Number of EUS-FNB tumour samples confirmed by D-FF-OCT, compared with the total number of samples taken.

    Measured: Day 1

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted31 Oct 2024
  2. Study start27 Jan 2025
  3. Primary completionJan 2027 (estimated)
  4. Study completionFeb 2027 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Basic science
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrolment
60 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06666803
Sponsor's protocol ID
23-003
Other IDs
2024-A00903-44
Status last verified
Apr 2026
First submitted
23 Oct 2024
Last updated
16 Apr 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing FNB sampling and blood sampling in people with PDAC - Pancreatic Ductal Adenocarcinoma, run by IHU Strasbourg at 2 sites in France.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 5 inclusion and 9 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 16 Apr 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 2 sites in France. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Armelle TAKEDA (+33390413608, armelle.takeda@ihu-strasbourg.eu), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Organoid culture from PDAC EUS-FNB biopsy (time frame: 8 weeks). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 16 Apr 2026.

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