AI Evaluation of Pancreatic Exocrine Insufficiency in CP Patients

February 22, 2024 updated by: Changhai Hospital

Artificial Intelligence Assistance of Pancreatic Exocrine Insufficiency Evaluation in Chronic Pancreatitis From Contrast-Enhanced CT

Early assessment of pancreatic exocrine insufficiency (PEI) is crucial for determining appropriate chronic pancreatitis (CP) treatment plans, thereby avoiding unnecessary suffering and further complications in patients. A total of 504 patients with CP who underwent fecal elastase-1 test and contrast-enhanced CT at Changhai Hospital between January 2018 and April 2023 were enrolled in this study. The investigators aim to establish a fully automated workflow to establish a PEI classification model based on radiomic features, semantic features and deep learning features on enhanced CT images for evaluating the severity of PEI.

Study Overview

Detailed Description

Chronic pancreatitis (CP) is a chronic inflammatory disease characterized by abdominal pain, recurrent inflammation, and pancreatic fibrosis. The global incidence of CP is about 10/100,000 and shows an increasing trend year by year.

Pancreatic exocrine insufficiency (PEI) is a significant functional alteration in chronic pancreatitis. The prevalence of PEI in CP patients within 10 to 15 years after diagnosis is about 35% to 50%, and the prevalence increases significantly 15 years after diagnosis.Clinical manifestations of PEI vary among individuals and may include symptoms such as diarrhea, weight loss, abdominal pain, bloating, and steatorrhea. Some patients may remain asymptomatic, leading to deficiencies in fat-soluble vitamins and micronutrients due to abnormal digestion of macronutrients, a condition referred to as "subclinical PEI".Due to nutritional deficiencies, PEI patients are at an increased risk of complications related to malnutrition, osteoporosis, cardiovascular diseases, and elevated mortality rates. Importantly, the quality of life for PEI patients is significantly reduced, and timely diagnosis and treatment are crucial to prevent severe consequences. Early and appropriate use of pancreatic enzyme replacement therapy can enhance patient well-being and improve overall quality of life. Therefore, regular screening for PEI and prompt treatment are essential for CP patients to reduce the risk of complications and improve prognosis.It is recommended by current clinical guidelines that pancreatic exocrine function should be assessed at the time of CP diagnosis, and if no PEI is detected, annual screening is advised. Despite these recommendations, PEI is still frequently misdiagnosed and inadequately treated in clinical practice.

Pancreatic exocrine function testing involves both direct and indirect methods. Direct tests, such as the cholecystokinin-pancreozymin stimulation test, are considered the most sensitive and specific means of assessing pancreatic exocrine function. This test requires intravenous infusion or injection of cholecystokinin to stimulate pancreatic secretion, followed by duodenal content collection via a catheter for the measurement of pancreatic fluid secretion. However, due to its high cost, invasiveness, and significant discomfort for patients, this test is seldom used in clinical practice.Indirect tests encompass fecal tests, breath tests, urine tests, and blood tests. Among these, fecal elastase-1 (Fe-1) detection is a currently stable, accurate, and convenient indirect method. When Fe-1 levels range between 100-200 μg/g, it suggests mild to moderate PEI, while Fe-1 levels below 100 μg/g indicate severe PEI. Several studies have demonstrated that a Fe-1 level below 200 μg/g has a specificity greater than 90% for diagnosing PEI. However, the limited availability of the assay kit has restricted its widespread use.

In imaging examinations, the use of secretin-enhanced magnetic resonance cholangiopancreatography to measure pancreatic fluid flow after secretin stimulation is a non-invasive method for assessing PEI. However, its clinical feasibility is limited due to its time-consuming nature, high cost, complexity, and the lack of widespread availability of the required reagents. Computed Tomography (CT) is the most widely used imaging examination in the clinical assessment of CP, but there is no evidence supporting its utility in detecting PEI. Therefore, there is a need for a new, non-invasive, and convenient method for early detection of PEI.

In recent years, deep learning has shown significant promise in medical image analysis. Compared to traditional machine learning, deep learning utilizes models to analyze data and extract higher-level features. It then uses these features to derive results, enabling the modeling of complex relationships within the data. Commonly used methods include convolutional neural networks, generative adversarial models, and others. Currently, deep learning has been widely applied in pancreatic diseases, including tumor detection, differential diagnosis of pancreatic cancer, and predicting patient prognosis. However, there has been no research utilizing deep learning to assess PEI.This study aims to develop and validate a deep learning model based on fully automated pancreatic segmentation for evaluating pancreatic exocrine function. Additionally, The investigators will collaborate with radiologists to jointly assess the model's performance.

Study Type

Observational

Enrollment (Actual)

504

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Shanghai, China, 200433
        • Changhai Hospital

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Sampling Method

Non-Probability Sample

Study Population

A total of 504 patients with CP who underwent the FE-1 test and CE-CT at Changhai Hospital between January 2018 and April 2023 were enrolled in this study. the exclusion criteria were as follows: (a) enhanced CT was taken during the acute episode of chronic pancreatitis, (b) history of malignant tumor, (c) previous pancreatic surgery, (4) systemic diseases, and (5) poor image quality or image loss

Description

Inclusion Criteria:

  • gender and age are not restricted
  • diagnosis of chronic pancreatitis
  • fe-1 test was conducted following recent pancreatic enhanced CT
  • sign informed consent

Exclusion Criteria:

  • enhanced CT was taken during the acute episode of chronic pancreatitis
  • history of malignant tumor
  • previous pancreatic surgery
  • systemic diseases
  • poor image quality or image loss

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Classification of pancreatic exocrine insufficiency
Time Frame: Up to 10 months
Pancreatic exocrine insufficiency are classified by FE-1 test into severe (0-100), mild to moderate (100-200) and normal (>200).
Up to 10 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

March 1, 2023

Primary Completion (Actual)

January 1, 2024

Study Completion (Actual)

January 1, 2024

Study Registration Dates

First Submitted

January 22, 2024

First Submitted That Met QC Criteria

February 22, 2024

First Posted (Estimated)

February 26, 2024

Study Record Updates

Last Update Posted (Estimated)

February 26, 2024

Last Update Submitted That Met QC Criteria

February 22, 2024

Last Verified

January 1, 2024

More Information

Terms related to this study

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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