Actively Recruiting

Age: 18Years +
All Genders
NCT06694792

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

Led by IRCCS San Raffaele · Updated on 2025-11-19

800

Participants Needed

1

Research Sites

103 weeks

Total Duration

On this page

Sponsors

I

IRCCS San Raffaele

Lead Sponsor

U

University of Pisa

Collaborating Sponsor

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

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

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adult (age >18 years) patients with a diagnosis of IPMN undergoing and not undergoing surgery
  • All patients will sign the informed consent
  • For retrospective patients: confirmed IPMN diagnosis
  • For retrospective patients: signed informed consent for samples biobanking and study participation
Not Eligible

You will not qualify if you...

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

AI-Screening

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Trial Site Locations

Total: 1 location

1

San Raffaele Hospital

Milan, MI, Italy, 20132

Actively Recruiting

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Research Team

S

Stefano Crippa, MD

CONTACT

G

Gabriele Capurso, MD

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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