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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04753229
Other study ID # TNE P Ki-IPC 2020-046
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 1, 2008
Est. completion date October 1, 2020

Study information

Verified date February 2021
Source Institut Paoli-Calmettes
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This is a retrospective, monocentric study involving 50 patients with pancreatic neuroendocrine neoplasia resected between January 2008 and June 2020 at Paoli Calmettes Institute. The primary objective of the study is to evaluate the grade concordance rate, based on Ki67 obtained on the pre-operative micro-biopsy and the surgical specimen. Based on the histology slides obtained in the course of the treatment, several Ki67 recounts will be performed on pre-operative tumor micro-biopsies and on tumors resected after surgery: - a manual count (on photo printed in the hotspot area according to World Health Organization (WHO) 2017 recommendations, by an expert pathologist and a junior pathologist. - Automated counting using specific software based on artificial intelligence (Qpath software). On the other hand, clinical, surgical and anatomopathological data will be collected in order to follow the patient evolution.


Recruitment information / eligibility

Status Completed
Enrollment 50
Est. completion date October 1, 2020
Est. primary completion date October 1, 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Patients with resection of pancreatic neuroendocrine neoplasia by surgery at Paoli Calmettes Institute between January 2008 and June 2020 - Patients who had a pre-surgical evaluation of Ki67 on micro-biopsy equipment obtained by echo-endoscopy. Exclusion Criteria: - Patient with a mixed tumor of the pancreas. - Patient with a pancreas tumor composed of several nodules of similar size without a main mass and for which it is not possible to determine the biopsied nodule during echo-endoscopy. - Initial micro-biopsy in a private pathology laboratory - Initial subechoendoscopic puncture cytology only (Ki67 not possible) - No initial micro-biopsy and surgery

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Institut Paoli-Calmettes

Outcome

Type Measure Description Time frame Safety issue
Primary Ki67 Grade Evaluation by a pathologist by manual counting according to WHO 2017 recommendations on pre-operative micro-biopsies
Primary Ki67 Grade Evaluation by a pathologist by manual counting according to WHO 2017 recommendations on surgical specimens
Secondary Percentage of Ki67 positive cells on total counted cells Evaluation by a pathologist by manual counting according to WHO 2017 recommendations on preoperative micro-biopsies
Secondary Percentage of Ki67 positive cells on total counted cells Evaluation by a pathologist by manual counting according to WHO 2017 recommendations on surgical specimens
Secondary Percentage of Ki67 positive cells on total counted cells Evaluation by digital pathology before and after machine learning on preoperative micro-biopsies
Secondary Percentage of Ki67 positive cells on total counted cells Evaluation by digital pathology before and after machine learning on surgical specimens
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