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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT04024358
Other study ID # VANISSh
Secondary ID
Status Active, not recruiting
Phase
First received
Last updated
Start date January 1, 2015
Est. completion date January 1, 2025

Study information

Verified date March 2024
Source IRCCS San Raffaele
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The aim of this study is to validate both retrospectively and prospectively a newly proposed scoring system for perineural and vascular invasion in pancreatic ductal cancer and correlate it with disease free survival, early recurrence, site of recurrence, overall survival and neoadjuvant treatment.


Description:

Perineural invasion (PNI) is defined as the presence of cancer cells along nerves and/or within the epineural, perineural and endoneural spaces of the neuronal sheath.Clinically, PNI is associated with increased tumor recurrence, poor survival after pancreatectomy and pain, an invalidating symptom that may impair quality of life. Pancreatic ductal adenocarcinoma has one of the highest incidences of PNI (70-100%) among all types of cancer, which correlates with a poor prognosis and decreased survival. PNI is a still not uniformly characterized or quantified event, usually it is described only dichotomously ("present" or "absent"), despite some efforts to use a more detailed scoring system. However, these scores are not specifically developed for pancreatic surgical specimen. Vascular invasion (VI), which is assumed to be associated with a more aggressive tumor biology and dissemination, lacks a specific scoring system as well. The primary aim of this study is to validate both retrospectively and prospectively a novel PNI and VI scoring system aimed at a more detailed stratification of perineural invasion, together with an accompanying scoring system for vascular invasion, and correlated them with disease free survival (DFS).


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 500
Est. completion date January 1, 2025
Est. primary completion date January 1, 2025
Accepts healthy volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Patients older than 18 years - Patients undergoing all types of pancreatic resection (pancreatoduodenectomy, left pancreatectomy, total pancreatectomy, both laparotomic and laparoscopic). - Proven pancreatic ductal adenocarcinoma (cytology or biopsy). - Patients that received neoadjuvant therapy (CT +/- RT) can be included. - Patients able to sign the informed consent. Exclusion Criteria: - Age < 18 years. - Patients with other ongoing oncological diseases.

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Italy IRCCS San Raffaele Milan

Sponsors (1)

Lead Sponsor Collaborator
Massimo Falconi

Country where clinical trial is conducted

Italy, 

Outcome

Type Measure Description Time frame Safety issue
Primary PNI and VI correlation with DFS Analyze if the severity of perineural and perivascular invasion correlates with disease free survival Up to 36 months
Secondary PNI and VI correlation with other clinical variables Analyze if the severity of perineural and perivascular invasion correlates with major clinical variables such as early recurrence, site of recurrence, overall survival. Up to 6 years
Secondary PNI and VI correlation with neoadjuvant treatment Analyze if neoadjuvant treatment impacts the severity of perineural and perivascular invasion. Up to 12 months
Secondary Correlation of neurotoxicity with PNI For patients undergoing chemotherapeutic treatment, correlate (if experienced) neurotoxic side effects with PNI presence and scoring system to treatment response Up to 12 months
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