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Pancreatic Cancer ResectableNCT06287749

French Assessment of MRD by Liquid Biopsies in PDAC Patients (FRENCH.MRD.PDAC)

An observational study of Pancreatic Cancer Resectable and Pancreatic Ductal Adenocarcinoma, run by University Hospital, Montpellier at 1 site 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

The overall objective of this GUIDE.MRD consortium is to confirm that ctDNA detected after curative intended treatment for PDAC is a marker of residual disease and for risk-of-recurrence, and applicable in clinical practice. Read more about this study

Who is it for?
Ages 18 years and older
What is being tested?
Blood sample/Liquid Biopsy
How many people
37 participants
Where
1 siteFrance
Study dates
1 Mar 2024to 31 Oct 2028
Phase
Observational
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

Study population: Patients with resected PDAC

Who may be able to join

  • Pancreatic ductal adenocarcinoma, according to the assessment of the MDT.
  • Age 18 years or older.
  • Scheduled for curative intent surgical resection.

Who cannot join

  • Hereditary pancreatic cancer.
  • Verified distant metastases.
  • Patients who are unlikely to comply with the protocol (e.g. uncooperative attitude), inability to return for subsequent visits and/or otherwise considered by the Investigator to be unlikely to complete the study.
  • Other cancers (excluding prior pancreatic cancer or skin cancer other than melanoma) within 3 years from eligibility screening.
  • Pregnant or nursing woman, or in childbearing age and not willing to use contraception
  • Adult subject to a legal protection
  • Not covered by Health insurance
  • Patient unable to understand and sign written informed consent.

Trial locations and contacts

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

Catherine ALIX-PANABIERES, Ph.D contact

+33411759931

c-panabieres@chu-montpellier.fr

Thomas BARDOL, M.D. contact

+33467339069

t-bardol@chu-montpellier.fr

France1 site, 1 recruiting
  • CHU de Montpellier

    Montpellier, Hérault, 34295

    Catherine PANABIERES, +33411759931, panabieres@chu-montpellier.fr

    Recruiting

Other trials in France

About this study

Official title: French Assessment of Minimal Residual Disease by Liquid Biopsies in Pancreatic Ductal Adenocarcinoma Patients

The overall objective of this GUIDE.MRD consortium is to confirm that ctDNA detected after curative intended treatment for PDAC is a marker of residual disease and for risk-of-recurrence, and applicable in clinical practice.

Primary objective To confirm that ctDNA analyses performed after PDAC treatment can identify patients with a high risk-of-recurrence.

Specifically, the investigators want to determine the association between disease-free survival (DFS) and ctDNA detection status after

  1. curative-intended surgery and
  2. adjuvant chemotherapy.

FRENCH.MRD.PDAC is the French study of the european GUIDE.MRD project

Read the detailed description

PDAC is the most common subtype of pancreatic cancer. The main pillars of non-metastatic PDAC clinical management are (i) surgery and (ii) neoadjuvant treatment including chemotherapy, which can be followed by external radiotherapy in case of borderline/locally advanced tumors.

Adjuvant chemotherapy is standard-of-care and is given to most patients that tolerate it after the extensive surgical procedure. The sequence of perioperative chemotherapy (before, after, both) is currently a matter of debate.

Despite extensive surgical resection and chemotherapy, most patients relapse, and median overall survival in the group of patients that is treated with surgery and modern chemotherapy regimens is below 24 months.

Throughout the body, DNA is released from cells into the circulation. This DNA is collectively referred to as cell-free DNA (cfDNA). In a patient with a solid cancer such as PDAC, a fraction of the cfDNA found in the blood, originates from tumor cells, and is termed circulating tumor DNA (ctDNA).

At present, a multitude of different ctDNA tests are available, and a common standard is lacking. This study is part of the large, EU-funded GUIDE.MRD project that aims to develop international reference standards for ctDNA diagnostics and use the best, standardized tests in clinically meaningful scenarios, including postsurgery follow-up of patients with PDAC, colorectal cancer, and lung cancer.

Detailed Description:

The FRENCH.MRD.PDAC study will prospectively enroll patients in France who undergo potentially curative surgery for PDAC. The intervention is repeated blood sampling at pre-defined time points.

Primary objective To confirm that ctDNA analyses performed after PDAC treatment can identify patients with a high risk-ofrecurrence.

Specifically, the investigators want to determine the association between 3-year disease-free survival (DFS) and ctDNA detection status after

  1. curative-intended surgery and
  2. adjuvant chemotherapy.

Secondary objectives Secondary objective 1 (S1) To technically assess, compare, and rank existing commercial ctDNA diagnostics after intended curative PDAC treatment (upfront surgery or neoadjuvant treatment followed by surgery +/- postoperative chemotherapy) to identify the best method at each time point, with no impact on diagnosis or treatment of patients enrolled in the study.

Secondary objective 2 (S2) To assess the effect of standard-of-care adjuvant chemotherapy on the level of ctDNA. Especially, for patients with ctDNA detected after surgery, the investigators will measure and compare the ctDNA levels in plasma samples drawn before and after adjuvant chemotherapy. Furthermore, the change in ctDNA level will be correlated to the oncological outcomes (time to clinical recurrence, disease-free survival, and overall survival).

Secondary objective 3 (S3) To investigate if time to Molecular recurrence determined using serial ctDNA analyses in longitudinally collected plasma samples is shorter than time to Clinical recurrence using standard-of-care radiological imaging.

Secondary objective 4 (S4) To investigate the correlation between ctDNA analysis results and findings on CT scans. ctDNA analysis will be restricted to blood sampling times that are coinciding with standard-of-care CT scans. If ctDNA analysis can predict the outcome of the CT scan, the potential is that ctDNA analysis in the future can guide when to perform CT scans.

Secondary objective 5 (S5) To investigate the prognostic power of ctDNA at the time point of indeterminate CT scans.

Patient identification Patients with PDAC are screened for eligibility by the involved physicians based on the protocol of the multidisciplinary tumor board (MDT). The screening will be done based on the electronic health record in the electronic journal (at present, for example, Take Care). The National Health Record may be accessed for some patients to complete the record.

Patient recruitment and informed consent The involved physicians screen patients meeting the inclusion criteria specified below. Eligible patients are approached in person or initially by phone, after they have been informed about the diagnosis and the planned surgery. Patients are given written and oral information about the project by a trained research nurse or by an involved physician. Informed consent will be obtained before the beginning of any study-related procedures.

The signed and dated consent forms are scanned into the project's electronic database and stored physically in a locked space.

Being tested
Blood sample/Liquid Biopsy
Keywords
Pancreatic Ductal Adenocarcinoma, Pancreatic Cancer Resectable, Minimal Residual Disease, Liquid Biopsy, ctDNA
Medical subject headings
Neoplasm, Residual

What participants receive

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

  • Blood sample/Liquid BiopsyBiological

    ctDNA analysis

Study groups in NCT06287749
Study groupRoleWhat they receive
Pancreatic Ductal Adenocarcinoma patientsResectable PDAC patients
Receives: Biological: Blood sample/Liquid Biopsy

What is being measured

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

  1. 3-year Disease-free survival (DFS)

    Disease-free survival was defined as the time between the date of the baseline blood sampling/inclusion and the date of the first event among or recurrence or death from any cause.

    Measured: 3 years after the end of inclusion

Secondary outcomes (8)
  1. Sensitivity (Se) of the ctDNA diagnostics

    Sensitivity (Se) of the ctDNA diagnostics is calculated in subjects with a 3-year recurrence: Se = TP/(TP+FN) (a positive reference test)

    Measured: 3 years after the end of inclusion

  2. Specificity (Sp) of the ctDNA diagnostics

    Specificity (Sp) of the ctDNA diagnostics is calculated in subjects without a 3-year recurrence: Sp = TN/(TN+FP) (a negative reference test)

    Measured: 3 years after the end of inclusion

  3. Positive predictive value of the ctDNA diagnostics

    The predictive value of a positive test or positive predictive value (PPV): PPV = TP/(TP+FP).

    Measured: 3 years after the end of inclusion

  4. Negative predictive value of the ctDNA diagnostics

    The predictive value of a negative test or negative predictive value (NPV): NPV =TN/(TN+FN).

    Measured: 3 years after the end of inclusion

  5. Are Under the Curve of the ctDNA diagnostics

    Area Under the Curve of the of the ctDNA:

    • AUC ≤0.75 = low classification accuracy,
    • 0.75 < AUC < 0.85 = moderate accuracy,
    • and AUC ≥0.85 = high accuracy

    Measured: 3 years atfer the end of inclusion

  6. Time to clinical recurrence

    Time to clinical recurrence was defined as the time between the date of the baseline blood sampling/inclusion [debut] and the date of the recurrence.

    Measured: 3 years after the end of inclusion

  7. Overall survival

    Overall survival was defined as the time between the date of the baseline blood sampling/inclusion [debut] and the date of death from any cause.

    Measured: 3 years after the end of inclusion

  8. Time to molecular recurrence

    Time to molecular recurrence was defined as the time between the date of the baseline blood sampling/inclusion [debut] and the date of the molecular recurrence (positive ctDNA test).

    Measured: 3 years after the end of inclusion

Timeline

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

  1. First posted1 Mar 2024
  2. Study start1 Mar 2024
  3. Primary completion31 Oct 2028 (estimated)
  4. Study completion31 Oct 2028 (estimated)

Resources

More details

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

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
37 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06287749
Sponsor's protocol ID
RECHMPL23_0298
Status last verified
Jul 2025
First submitted
8 Feb 2024
Last updated
10 Jul 2025
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

An observational study of Pancreatic Cancer Resectable and Pancreatic Ductal Adenocarcinoma, run by University Hospital, Montpellier at 1 site 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 3 inclusion and 8 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 10 Jul 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site 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 Catherine ALIX-PANABIERES, Ph.D (+33411759931, c-panabieres@chu-montpellier.fr), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

3-year Disease-free survival (DFS) (time frame: 3 years after the end of inclusion). 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 10 Jul 2025.

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