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Intraductal Papillary Mucinous Neoplasm of PancreasEMI-IPMNNCT06706700

Endocrine, Metabolic, Inflammatory Biomarkers to Identify Highgrade Dysplasia/invasive Carcinoma in Patients with IPMN of the Pancreas

An observational study of Intraductal Papillary Mucinous Neoplasm of Pancreas and Pancreatic Cyst, run by IRCCS San Raffaele at 1 site in Italy.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

Under the hypotheses that a more accurate patients selection could limit the problem of overtreatment and that benign intraductal papillary mucinous neoplasms (IPMN) have a distinguishable Endocrine/Metabolic/Inflammatory (EMI) profile from those with high-grade disease/invasive carcinoma, this study has three… Read more about this study

Who is it for?
Ages 18 years and older
How many people
586 participants
Where
1 siteItaly
Study dates
13 Jul 2020to 31 Mar 2025
Phase
Observational
Are there results?
None posted in the registry

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: The patients will be enrolled in the outpatient clinic, if they meet the required criteria for inclusion.

Who may be able to join

  • Age >= 18 years
  • Charlson comorbidity index <7
  • indication for surgery for suspected IPMN

Who cannot join

  • lack of preoperative clinical and radiological data according the two guidelines
  • Cohort B and C:

Trial locations and contacts

1 site in 1 country.

Italy1 site, 1 recruiting
  • San Raffaele Hospital

    Milan, Italy, 20132

    Stefano Crippa, MD, +39 0226436046, crippa.stefano@hsr.it

    Stefano Crippa, MD

    Recruiting

Other trials in Italy

About this study

Official title: Definition of Radiological and Endocrine/metabolic/inflammatory Biomarker(s) to Identify Highgrade Dysplasia/invasive Carcinoma in Patients with Intraductal Papillary Mucinous Neoplasms of the Pancreas

Under the hypotheses that a more accurate patients selection could limit the problem of overtreatment and that benign intraductal papillary mucinous neoplasms (IPMN) have a distinguishable Endocrine/Metabolic/Inflammatory (EMI) profile from those with high-grade disease/invasive carcinoma, this study has three specific aims. The first aim is to evaluate and confirm the accuracy of the updated versions of International and European guidelines for the management of IPMN and it will be addressed by retrospectively applying the criteria included in the two guidelines on 350 patients with resected IPMN in order to determine the most accurate criteria to identify High Grade Dysplasia(HGD)/Invasive Carcinoma (IC).

The second aim is to identify pre-operative biological and/or radiological/endosonographic biomarker(s) able to distinguish low- versus high-risk IPMN for cancer progression in a prospective study by enrolling a cohort of 186 (of which 145 surgically-resected) patients.

The third aim is to prospectively validate biological and/or radiological/endosonographic biomarker(s) (previously identified and optimized) on a new cohort of 50 patients with IPMN undergoing surgical resection.

Read the detailed description

Up to 40% of patients (pts) undergoing abdominal imaging harbor unsuspected pancreatic cysts, the majority of which intraductal papillary mucinous neoplasms (IPMN). IPMNs are well-known precursors of pancreatic ductal adenocarcinoma (PDAC) without an established temporal window of progression. Current guidelines identify high-risk stigmata (HRS)/absolute criteria(AC) and worrisome features(WF)/relative criteria(RC) as indications for surgical resection of IPMN. Previous guideline criteria were found to be associated with high sensitivity but low specificity for malignancy, resulting in an overtreatment of benign IPMNs, a clinical relevant issue considering the high morbidity/mortality of pancreatectomy. Currently, there are no available hematic biomarkers in peripheral blood, be they DNA, RNA or protein-based, which can identify High Grade Dysplasia(HGD)/Invasive Carcinoma (IC). DNA-based molecular testing of pancreatic cyst fluid obtained during endoscopic ultrasound (EUS)/surgery have been developed and are used to identify advanced neoplasia, with good sensitivity/specificity, and therefore hypothetically, an IPMN HGD/IC-based biomarker could be more readily detected in cyst fluid or in portal blood. This strategy, however has a number of limitations: i) it is highly invasive and costly ii) poor quantity and quality of cyst fluid may lead to incorrect detection (false negatives in molecular testing) ; and iii) a lack of predictive potential of progression over time. New diagnostic tools based on samples of portal blood obtained during EUS or potentially peripheral samples (of new biomarkers) may overcome these limitations.

PDAC has been associated with altered inflammatory and endocrine/metabolic profiles but limited data are available on IPMN and other precursors. Inflammation and malignant progression have become cardinal in cancer research. Tumor-associated neutrophils and cytokines, including TNFalpha and IL-1ß, have been associated with malignant progression also in IPMN. About 40-70% of patients with PDAC experience diabetes or alterations of glucose homeostasis. Diabetes-induced hyperglycemia, hyperinsulinemia, altered insulin-like growth factors production, chronic inflammation and metabolic syndrome have been associated with cancer . In a large cohort of resected IPMNs, preoperative diabetes was significantly associated with HGD/IC, and the risk of IC was highest in patients with recent-onset diabetes.

Obesity is also a well-known risk factor for PDAC; proinflammatory cytokines, known as adipokines are released mainly from visceral adipose tissue stimulating aberrant angiogenesis. An association between visceral obesity and pancreatic fatty infiltration with poor survival was found in PDAC patients. In the setting of IPMN, in a very small cohort of resected patients, significantly higher BMI was associated to an increased rate of malignant IPMN.

EUS, Computed tomography(CT) and magnetic resonance imaging(MRI) are of use in current clinical practice to study and monitor pancreatic diseases. They are all imaging techniques that allow to characterize pancreatic alterations and simultaneously detect endocrino-metabolic alterations (i.e.visceral obesity, liver steatosis, pancreatic fatty infiltration) that may be associated to pancreatic diseases.

Current literature is still debating the superiority of radiological imaging (specifically MRI) or endoscopic ultrasound in identifying worrisome features/high risk stigmata and in correctly distinguishing benign/malignant IPMNs. Preliminary analysis performed in the context of this study, specifically in retrospective Cohort A, aimed at validating International and European guidelines, supports an important role for EUS in identifying risk of malignancy in IPMNs. In fact, 31/116 patients (26.7%) with WF at MRI were "upstaged" by EUS and the majority of these (77.4%) had malignancy at final pathology. Furthermore, EUS confirmed MRI findings in 87.5% of cases, including 72.4% of radiological WF.

The association among obesity, diabetes, inflammation, alterations of specific endocrine/metabolic pathways and pancreatic cancer development from its precursors (IPMN) are more complex, and needs further investigations.

The driving hypotheses of this study are that i) a more accurate patients selection could limit the problem of overtreatment, ii) that benign/indolent IPMN have a distinguishable Endocrine/Metabolic/Inflammatory (EMI) profile from those with HGD/IC, and therefore this research has the following three specific aims.

Aim 1: To retrospectively evaluate and to validate the updated versions of International and European guidelines for the management of IPMN (Cohort A) Aim 2: To identify pre-operative biological and/or imaging biomarker(s) to distinguish low- versus high-risk IPMN for cancer progression in a prospective study of surgically-resected patients (Cohort B) Aim 2.1: To compare MRI and EUS in the pre-operative evaluation of IPMNs and with respect to pathological findings. In particular, primary endpoint will be the identification of main pancreatic duct involvement. Secondary endpoints will be evaluation of the degree of main duct involvement (extension of IPMN involvement, MPD diameter at predetermined points, maximum diameter of MPD), the presence of thickened ductal walls, mural nodules and the characteristics of the surrounding parenchyma (fatty infiltration/vanishing pancreas).

Aim 3: To prospectively validate biological and/or imaging biomarker(s) previously identified (Aim 2) on patients with IPMN undergoing surgical resection (Cohort C)

Keywords
ipmn, intraductal papillary mucinous neoplasm of the pancreas, Pancreatic Cysts
Medical subject headings
Pancreatic Intraductal Neoplasms, Pancreatic Cyst

What participants receive

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

Study groups in NCT06706700
Study groupRoleWhat they receive
Cohort AA retrospective study of a cohort of 350 resected patients with a histologically-confirmed IPMN, diagnosed from the 1st January 2009 to the 31st May 2018 following these inclusion criteria: * histologically proven IPMNs with full pathological data (type of IPMNs, grade of dysplasia; for invasive IPMNs: grading, pTNM classification, presence of perineural (microvascular infiltration) * availability of clinical and imaging criteria for surgical resections defined by International and European guidelines (worrisome features and high-risk stigmata according to International Guidelines and absolute/relative criteria for surgery according to European guidelines * age ≥18 years and exclusion criteria: * lack of preoperative clinical and radiological data according the two guidelines
Cohort BA prospective observational study whose aim is to identify EMI profiles and radiological/endosonographical biomarker(s) associated to surgically removed IPMNs with HGD/IC. Patients diagnosed with IPMN and candidates for resection with following inclusion criteria will be enrolled: * Age >= 18 years * Charlson comorbidity index <7 [26] The patients' cohort will be selected following the best criteria for surgery identified in the retrospective study (Cohort A). At the admission, patients will be informed by PI, or his delegates about the study, and they will be asked to sign the specific informed consents (see par. 5.1) In the course of standard pre-operative evaluation, all patients will undergo MRI and EUS, within no more than 3 months between exams.
Cohort CA prospective study with the aim to validate potential biomarker(s) identified in the Cohort B. Patients with a diagnosis of IPMN candidate for resection with the following inclusion criteria will be enrolled: * Age >= 18 years * Charlson comorbidity index <7 [26] The patients' cohort will be selected following the best criteria for surgery identified in the retrospective study (Cohort A). At the admission patients will be informed by PI or his delegates about the study and they will be asked to sign specific informed consents

What is being measured

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

  1. evaluation of the best guideline between the International and European guidelines

    The criteria included in the two guidelines will be retrospectively applied on 350 patients with resected IPMN. Clinical pathological and imaging data will be retrieved from institutional archives systems.

    As we may be not able to identify a more accurate guideline, we may select specific criteria from each of the two guidelines, thus selecting p batients for surgery based on a combination of criteria from both guidelines.

    The identified best criteria will be applied to select the discovery cohort and the validation cohort of the prospective studies.

    Measured: from the collection of the retrospective cohort to 12 months

  2. endocrine, metabolic and inflammatory profile

    The following parameters will be measured in peripheral and portal serum/plasma and in the cyst fluid with commercially available kits

    Measured: from the enrollment to 8 month

  3. imaging-based biomarker(s)

    As per standard-of-care current clinical practice in our institution, all patients will undergo 1.5T contrast-enhanced MR cholangiopancreatography (MRCP) with 3D acquisition protocol of the pancreatic ducts/ biliary tree

    Measured: at the time of enrollment

  4. evaluation of the accuracy of the biomarkers in predicting the pathological diagnosis

    the accuracy at identifying malignant IPMN of the identified biomarkers will be tested.

    Measured: at the end of the enrollment

Secondary outcomes (1)
  1. evaluation of the accuracy of the MRI versus the EUSP in identifying the involvement of the main pancreatic duct

    Measured: at the end of the enrollment

Timeline

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

  1. First posted26 Nov 2024
  2. Study start13 Jul 2020
  3. Primary completion31 Jan 2025 (estimated)
  4. Study completion31 Mar 2025 (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
586 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06706700
Sponsor's protocol ID
EMI-IPMN
Acronym
EMI-IPMN
Status last verified
Oct 2024
First submitted
22 Nov 2024
Last updated
26 Nov 2024
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Yes

Questions about this trial

What is this clinical trial studying?

An observational study of Intraductal Papillary Mucinous Neoplasm of Pancreas and Pancreatic Cyst, run by IRCCS San Raffaele at 1 site in Italy.

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 2 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: status not confirmed, as of the sponsor's last update on 26 Nov 2024. 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 Italy. 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?

Results are not available in the source record.

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

Contact Stefano Crippa, MD (+39 0226437811, crippa.stefano@hsr.it), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

evaluation of the best guideline between the International and European guidelines (time frame: from the collection of the retrospective cohort to 12 months). The study lists 4 primary outcomes in all. 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 26 Nov 2024.

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