Integration of Multiomics Markers for Invasive IPMNs Identification Through the Set-up of the INvasive Cyst bIomarkers Detection (INCITE) Consortium

NCT ID: NCT06694792

Last Updated: 2025-11-19

Basic Information

• Recruitment Status: RECRUITING
• Total Enrollment: 800 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2025-01-03
• Study Completion Date: 2026-12-31

Brief Summary

Although intraductal papillary mucinous neoplasms (IPMNs) represent potential precursors of pancreatic cancer, IPMNs with invasive cancer are rare. Based on current risk factors for malignancy, overtreatment (surgery) of benign IPMNs remains a critical issue, with its associated risk of postoperative and long-term complications.

Identification of biomarkers that could predict malignancy in IPMNs is an unmet clinical need. Environmental, lifestyle, genetics and metabolic factors may play a role in IPMNs carcinogenesis. Aims of the study are: 1) to analyze exposome, somatic/germline genetic variability, metabolomics and transcriptome profile in order to identify new biomarkers; 2) to use nonparametric epidemiologic approaches and machine learning algorithms to compute a progression score to offer clinicians an innovative tool towards the goal of a personalized medicine approach. In order to perform all the analysis we will set up the Invasive Cyst biomarker detection (INCITE) consortium, between the participant centers in order to collectively enroll an adequate number of patients to fulfill the previous aims.

The project is designed as an observational cross-sectional multicenter study with additional procedures. The analysis will be conducted on biological samples collected at a single time point. Some samples (500 patients: 160 surgical, 340 under surveillance) are already available in the consortium, having been collected in previous studies, while additional 300 (100 surgical and 200 under surveillance) patients will be prospectively enrolled during the first 12 months of the study.

The sample collection will take place during outpatient visit/EUS procedure for the surveillance cohort, while in the surgical cohort all the material will be retrieved during the surgery. The patients samples will be divided in two cohorts, the first will be a discovery cohort and the second one a validation cohort. The first cohort will consist in patients already collected. The validation cohort will include patients enrolled prospectively during the first year of the study.

Detailed Description

IPMNs are precancerous lesions frequently detected in elderly individuals. IPMNs that develop high grade dysplasia or invasive cancer are rare. In large cohorts, the 5-year incidence of high grade dysplasia/invasive cancer ranges between 1 and 3%. IPMNs resection is based on clinico-morphological parameters including worrisome features (WF) and high-risk stigmata (HRS), that are not precise since a large proportion of patients (up to 40% for WF and up to 20% for HRS) do not have cancer at final pathology, resulting in over-treatment. Therefore, the identification of IPMNs harboring malignancy is an unmet clinical need. The main goal of IPMNs management is the precise identification and treatment of lesions harboring invasive cancer and high-grade dysplasia, a pre-invasive condition. Of note, the surgical treatment of early invasive cancer arising in the background of an IPMN (i.e., microinvasive cancers) is potentially curative. Current guidelines identify WF and HRS as clinico-morphological features associated with an intermediate risk and high of malignancy, respectively. Unfortunately, these criteria have a low accuracy in identifying malignant IPMNs (accuracy of 60% for HRS and of 35% for WF), and this may result in undertreatment (no surgery in patients with malignancy) or overtreatment (unnecessary surgery in IPMNs with low-grade dysplasia). IPMNs affect mainly elderly people, who often present coexisting comorbidities. This is a relevant issue. Pancreatic surgery is associated with a risk of postoperative mortality (< 5 % in high-volume centers, but this rate may be much higher when considering low volume hospitals), and significant postoperative morbidity (50%), with long-term, clinically relevant complications, such as pancreatic insufficiency and diabetes, that may impair quality of life. In this scenario, a major unmet clinical need is the identification of biomarkers that allow a clear distinction between IPMNs at risk of being/becoming malignant, that actually require a surgical treatment, and those with minimal or no risk of cancer progression. It is unlikely that a single biomarker may be effective in doing so, while composite biomarkers may be more relevant. The expected results of this project will have a strong impact on several different levels. The most obvious is the ability to identify which patients with IPMNs will benefit from surgery. Defining a set of predictive biomarkers would be a crucial step towards the goal of creating a personalized approach for each patient. This approach will also emphasize the role of biology in addition to the usual patient-related features (age, comorbidities) and IPMN-related clinico-morphological parameters (WF and HRS). Furthermore, the multi omics approach of the INCITE consortium will shed light on the etiopathogenesis of the disease, especially considering the germline and somatic mutation analysis. In fact, the possibility to combine data from different sources will be invaluable to better understand the biology of IPMNs which is the first, obligated, step towards pancreatic cancer prevention as IPMNs represent a unique in vivo model of pancreatic carcinogenesis.

The main aims of the study are: 1) to analyze exposome, somatic/germline genetic variability, metabolomics and transcriptome profile in order to identify new biomarkers; 2) to use nonparametric epidemiologic approaches and machine learning algorithms to compute a progression score to offer clinicians an innovative tool towards the goal of a personalized medicine approach.

In order to fulfill all the aims of the study, the Invasive Cyst biomarker detection (INCITE) consortium will be set up between the participant centers.

The collection of samples is already ongoing at each UOs and the first aim is to bring together all the resources and create a common database and a common protocol for biobanking in order to carry out meaningful studies. So far, biological samples from 500 IPMNs have already been collected, among those 160 were surgically resected (50 invasive IPMNs, 40 high grade IPMNs and 70 low grade IPMNs), while 340 were under surveillance (255 were collected at the Pancreatobiliary Endoscopy unit of HSR, and other 85 at the endoscopy unit of ISMETT). During the first 12 months of the project, considering the current rate of recruitment, we will enroll another 100 IPMN undergoing surgical resection (30/40% rate of invasive tumors) and 200 under surveillance. All the centers will participate in the enrollment in a competitive manner. All samples will be stored and processed in the same manner. Whole blood, plasma/serum, cyst liquid and, in patients who undergo surgical resection, pancreatic tissue samples will be collected for all individuals. For patients that have been already recruited, biological material will be collected during the next routine appointment. The expertise of all UOs in collaborative projects and in coordinating consortia will make this aim feasible in the time that this project application imposes.

All the analyses described in the previous section will be carried out in the discovery (n=100 resected IPMNs) set. To achieve this, materials from each center will be sent to other units for their specific analyses. Each unit will carry out the tasks within its area of expertise, as mentioned previously. The Material Transfer Agreement (MTA) will be arranged to facilitate the transfer of samples between all the different units. All analyses will be conducted in the discovery cohort, but only those yielding significant results will be performed in the validation cohort (n=150 resected IPMNs) An additional advantage of the INCITE consortium is the availability of a large cohort of patients under surveillance (255 were collected at the Pancreatobiliary Endoscopy unit of HSR, and other 85 at the endoscopy unit of ISMETT), that will allow us to test the presence/absence of invasive biomarkers also in this setting (i.e absence of these biomarkers in patients with IPMN lacking WF/HRS under surveillance with a minimum follow-up of 4 years without IPMN progression and presence of the biomarkers in patients under surveillance that develop indication for surgery). The exact analysis that will be carried out on this population will depend on the results obtained in the discovery cohort. The variables that will show a statistically significant association also in the validation set will be combined in a score as detailed in aim 2.

AIM 2 The second aim of this proposal is to perform data analysis and integration, and to combine in a progression score the variables that show a statistically significant association in the validation set of patients with IPMNs. The main challenge of the INCITE consortium will be integration of the data, especially considering their heterogeneous nature in order to do it we will develop a specific eCRF were all the different UOs will upload the results of their own analysis. The specific analysis, already described above, will be performed by UO4, with the help of all the other UOs. Both nonparametric epidemiologic approaches and statistical methods will be used. Additionally, permutational multivariate analysis of variance (PERMANOVA) will be used to cluster patients according to their features into different groups and therefore identify the most relevant features to explain invasiveness. Furthermore, artificial intelligence and machine learning algorithms will be used to compute a progression score. The exact nature of the algorithms used will depend on the data exploration and data understanding.

Duration of enrollment: 12 months Duration of subject participation: All the procedures on the patients will be carried out during the hospital stay for the surgical patients and during the EUS procedure for the patients under surveillance .

Duration of total study period: 24 months

Conditions

IPMN, Pancreatic

Study Design

• Observational Model Type: COHORT
• Study Time Perspective: PROSPECTIVE

Study Groups

discover cohort

The discover cohort will consist in patients already collected

No interventions assigned to this group

Validation cohort

The validation cohort will include patients enrolled prospectively during the first year of the study

No interventions assigned to this group

Eligibility Criteria

Inclusion Criteria

• Adult (age >18 years) patients with a diagnosis of IPMN undergoing and not undergoing surgery
• All patients will sign the informed consent

For the retrospective patients:

• confirmed IPMN diagnosis
• signed informed consent for samples biobanking and study participation

Exclusion Criteria

• Patients < 18 years of age
• Patients who are not able to supply an informed consent

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

University of Pisa

OTHER

Sponsor Role: collaborator

Casa Sollievo della Sofferenza IRCCS

OTHER

Sponsor Role: collaborator

The Mediterranean Institute for Transplantation and Advanced Specialized Therapies

OTHER

Sponsor Role: collaborator

IRCCS San Raffaele

OTHER

Sponsor Role: lead

Responsible Party

Stefano Crippa

Associate Professor

Responsibility Role: PRINCIPAL_INVESTIGATOR

Locations

San Raffaele Hospital

Milan, MI, Italy

Site Status: RECRUITING

Countries

Italy

Central Contacts

Stefano Crippa, MD

Role: CONTACT

crippa.stefano@hsr.it

+390226436046

Gabriele Capurso, MD

Role: CONTACT

capurso.gabriele@hsr.it

+390226436046

Facility Contacts

Francesca Di Salvo, PhD

Role: primary

disalvo.francesca@hsr.it

0226437810

Other Identifiers

INCITE

Identifier Type: -

Identifier Source: org_study_id