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What we learned from a decade of research on imaging of CP?

Temel Tirkes, MD, FACR, FSAR

Professor of Radiology & Imaging Sciences, Medicine and Urology

Chronic Pancreatitis - What Have We Learned From a Decade of Prospective MRI Research and AI?

Temel Tirkes, MD, FSAR, FACR 

Professor of Radiology & Imaging Sciences, Medicine and Urology

Ulas Bagci, PhD

Director of Machine & Hybrid Intelligence Lab

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Disclosures

NIH support

R01-DK116963 - Magnetic resonance Imaging as a Non-Invasive Method for Assessment of Pancreatic fibrosis (MINIMAP) study

U01-DK127382 - Type 1 Diabetes in Acute Pancreatitis Consortium

U01-DK108323 - Consortium for the Study of Chronic Pancreatitis, Diabetes, and Pancreatic Cancer

R01-CA260955 - Predicting Pancreatic Ductal Adenocarcinoma (PDAC) Using Artificial Intelligence Analysis of Pre-diagnostic Computed Tomography Images

R01-DK132631 - A Pilot Clinical Trial of Paricalcitol for Chronic Pancreatitis

Financial conflict: None

atirkes@iu.edu

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atirkes@iu.edu

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Publications on CP past 10 years

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atirkes@iu.edu

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MRI parenchymal features have better correlation with histopathology than ductal features by MRCP

MRI can detect CP earlier than MRCP

T1 signal of MRI correlates with severity of CP

Progression of CP is better seen in MRI than the MRCP

There is discordance of Cambridge grading between ERCP and MRCP

Better IOV needed for assessment of CP

Pancreatic fat can no longer be ignored

What have we learned

from a decade of research on

MR imaging of CP?

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Correlation of MRI Parenchymal Features with Histopathology

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MRI T1 signal vs MRCP Cambridge Score

Histopathology MRI T1 Signal Ductal Imaging

Abdom Radiol (NY). 2022 Jul;47(7):2371-2380. PMID: 35486166; Tirkes et. al.

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MRI T1 Score and Fibrosis

r = 0.54

MRCP Cambridge score and Fibrosis

r = 0.26

MRI T1 signal vs MRCP Cambridge Score

Abdom Radiol (NY). 2022 Jul;47(7):2371-2380. PMID: 35486166; Tirkes et. al.

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Correlation of MRI with fibrosis

r = 0.44

Am J Gastroenterol 2015; 110:1598–1606; doi: 10.1038/ajg.2015.297; September 2015

57 Adult patients underwent TPIAT for CP

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atirkes@iu.edu

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MRI parenchymal features have better correlation with histopathology than ductal features by MRCP

MRI parenchymal features can detect CP earlier than MRCP

T1 signal of MRI correlates with severity of CP

Progression of CP is better seen in MRI than the MRCP

There is discordance of Cambridge grading between ERCP and MRCP

Better IOV needed for assessment of CP

Pancreatic fat can no longer be ignored

What have we learned

from a decade of research on

MR imaging of CP?

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MRI and MRCP in suspected CP

MRI T1 signal correlated with HCO3

PFT was performed and HCO3 measured

MRCP showed Cambridge 0 or 1

RAP patients suspected to have CP

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T1 Signal in suspected CP

T1 SIR

RAP patients suspected of CP, but with normal MRCP

Lower T1 signal reflects low HCO3

Normal HCO3

Abnormal HCO3

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MRI T1 Signal changes

MRCP Ductal changes

Pre MRCP evident CP

CP before any ductal changes

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atirkes@iu.edu

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MRI parenchymal features have better correlation with histopathology than ductal features of MRCP

MRI parenchymal features can detect CP earlier than MRCP

MRI T1 signal correlates with severity of CP

Progression of CP is better seen in MRI than the MRCP

There is discordance of Cambridge grading between ERCP and MRCP

Better IOV needed for assessment of CP

Pancreatic fat can no longer be ignored

What have we learned

from a decade of research on

MR imaging of CP?

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PROCEED Study

MRI, MRCP and CT on 2,000 RAP/CP patients

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T1 Score (SIR of pancreas to spleen)

No CP

CP

Fat is suppressed. No contrast given. Performed in almost all MR examinations

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T1 Score (SIR) �is an imaging biomarker of CP

atirkes@iu.edu

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  • 820 MRIs in well-phenotyped control, RAP and definite CP
  • Included all MR vendors
  • Included 3.0T and 1.5T

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T1 Score decreases with increasing CP severity

Abdom Radiol (NY). 2022 Oct;47(10):3507-3519. PMID: 35857066. Tirkes, ae. al.

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T1 Score

T1 Score correlates with severity of CP

T1 score of 1.2 is the threshold

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atirkes@iu.edu

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MRI parenchymal features have better correlation with histopathology than ductal features by MRCP

MRI parenchymal features can detect CP earlier than MRCP

T1 signal of MRI correlates with severity of CP

Progression of CP is better seen in MRI than the MRCP

There is discordance of Cambridge grading between ERCP and MRCP

Better IOV needed for assessment of CP

Pancreatic fat can no longer be ignored

What have we learned

from a decade of research on

MR imaging of CP?

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Longitudinal Follow-up of CP

  • Patients with definitive CP had imaging follow-up of 4 years.
  • MR imaging parameters:
                  • Pancreatic volume
                  • DWI
                  • Fat signal fraction
                  • MPD diameter

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MRI vs MRCP for Follow-up of CP

Morphological progression of CP seems to be primarily parenchymal related

{

Pancreas volume decreased

Fat increased

MRI diffusion decreased

Ducts did not change

{

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atirkes@iu.edu

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MRI parenchymal features have better correlation with histopathology than ductal features by MRCP

MRI parenchymal features can detect CP earlier than MRCP

T1 signal of MRI correlates with severity of CP

Progression of CP is better seen in MRI than the MRCP

Discordance of Cambridge grading by ERCP vs MRCP

Better IOV needed for assessment of CP

Pancreatic fat can no longer be ignored

What have we learned

from a decade of research on

MR imaging of CP?

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Discordance of ERCP and MRCP interpretation

325 CP patients had MRCP and ERCP within 90 days

MRCP and ERCP based agreement of Cambridge score was only 43%

Conclusion

There is no satisfactory concordance between ERCP and MRCP-based Cambridge scores

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atirkes@iu.edu

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MRI parenchymal features have better correlation with histopathology than ductal features by MRCP

MRI parenchymal features can detect CP earlier than MRCP

T1 signal of MRI correlates with severity of CP

Progression of CP is better seen in MRI than the MRCP

Discordance of Cambridge grading between ERCP and MRCP

Better IOV needed for assessment of CP

Pancreatic fat can no longer be ignored

What have we learned

from a decade of research on

MR imaging of CP?

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Inter-observer agreement of Cambridge �by CT and MRCP

MR kappa = 0.68

CT kappa = 0.56

Composite CT/MR Kappa = 0.62

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MRI parenchymal features IOV

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Cambridge Classification - Weighted Kappa: 0.54

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atirkes@iu.edu

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MR Imaging Biomarkers for CP

MSCP 0 1 2 3 4 5 6

T1 Score 1.34 1.27 1.21 1.16 1.19 1.12 1.05

T1 ms (1.5T) 400 500 600 700 800

ECV (%) 10 20 30 40 50

Volume (ml) 80 70 60 50 40

AVR (art/ven) 1.4 1.3 1.2 1.1 1.0

Tail dm (cm) 2.5 2.4 2.3 2.2 2.1

CP-MRI Score 0 1 2 3 4 5

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atirkes@iu.edu

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MRI parenchymal features have better correlation with histopathology than ductal features by MRCP

MRI parenchymal features can detect CP earlier than MRCP

T1 signal of MRI correlates with severity of CP

Progression of CP is better seen in MRI than the MRCP

Discordance of Cambridge grading between ERCP and MRCP

Better IOV needed for assessment of CP

Pancreatic steatosis is evil

What have we learned

from a decade of research on

MR imaging of CP?

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atirkes@iu.edu

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Normal

CP

AC

Du

ICL

AC

Fib

Fat

Fat

Pancreatic steatosis and CP

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MRI Fat Quantification

Fat only image Water only image

Pancreas

PDFF is better than dual echo DIXON

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Pancreatic Fat and Adipose Tissue Quantification

Manual AI

Visceral and subcutaneous adipose tissues can be separated and measured either manually or AI tools

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Pancreatic steatosis, Obesity, and CP

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Pancreatic Steatosis

Pancreatitis

?

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atirkes@iu.edu

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Presenter: Prof. Ulas Bagci

Northwestern University, Machine and Hybrid Intelligence Lab, February, 2025

AI in Pancreas Imaging & Analysis

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Disclosures for Dr. Bagci

NIH support

R01-CA246704- Cyst-X: Interpretable Deep Learning based Risk Stratification of Pancreatic Cystic Tumors

U01-DK127384-02S1- Data Coordinating Center for the Type 1 Diabetes in Acute Pancreatitis Consortium-Imaging Morphology of Pancreas in Diabetic Patients following Patients with Acute Pancreatitis (IMMINENT) Study

Financial conflict: None.

atirkes@iu.edu

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Machine and Hybrid Intelligence Lab

  • Founded in 2021 January
  • School of Medicine, Dept of Radiology
  • Courtesy Biomedical Engineering, 
  • Courtesy Electrical and Electronics Eng, 
  • PI @ Lurie Cancer Center
  • Member – NIH AIR (AI in Resource)
  • Part of I.AIM (AI Institute at Northwestern)
  • 3 Large-scale servers (>30GPU)
  • ~30 members

www.bagcilab.com

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AI is needed for Pancreas Imaging Research for three primary tasks

  1. Standardization / Harmonization of Images
    • Heterogeneity of MRIs, scanner and acquisition differences, patient profiles, etc.
  2. Segmentation of Pancreas from radiology images (CT, MRI,...)
    • Compared to other organs, very challenging problem due to complex shape, sparse position, changing orientation, and poor signal in certain boundary locations
  3. Prediction algorithms
    • Diagnosis (a patient has this condition or no?)
    • Patient outcome prediction (a patient will have this condition or no?, will they respond to therapy? and similar questions)

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General Overview – How to Use AI in MRI Research of Pancreas

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General Overview – How to Use AI in MRI Research of Pancreas

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General Overview – How to Use AI in MRI Research of Pancreas

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General Overview – How to Use AI in MRI Research of Pancreas

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CP --> severity

or

No? --> future risk?

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  1. Harmonization / Preprocessing

atirkes@iu.edu

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2. Pancreas & Its Part Segmentation

  • Historically very difficult problem, most existing algorithms focus on CT imaging
  • Pancreas volumetry and its parts (head, body, tail) are critical to measure
  • Segmented pancreas can be used for auto-diagnosis and future-prediction with AI

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PanSegNet

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Summary of Contributions for PanSegNet

  • First ever multi-center, muti-site MRI pancreas segmentation algorithm
  • State of the art results are obtained!
  • 3D (volumetric) Algorithm
  • Code, Models, Data, and Labels are made public
  • Largest Cohort reported so far (>700 MRI with pubs, currently >1400 with updated version)
  • CP, Cyst, Diabetes, pediatric pancreatitis patients were all tested (>2000), it works also for PanCan patients CT (>2000)

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Inter- and Intra-observer Analysis of GT Labels

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CT Results (>88% dice accuracy)

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MRI T1 Results

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MRI T2 Results

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Out-of-Phase MRI Segmentation (>87% dice score)

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Pancreas Part Segmentation – Head/Body/Tail��>87% dice score

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Pediatric patients – pancreatitis (acute/chronic)

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Dice (SD)

ALL

0.85 (0.16)

Chronic Pancreatitis

0.80 (0.20)

Acute Pancreatitis

0.81 (0.19)

Normal

0.88 (0.1)

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Tumor / Cyst Segmentation ?

atirkes@iu.edu

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MICCAI AIPAD 2024

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3-AI and Radiomics for Diagnosis and Prognosis

atirkes@iu.edu

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Radiomics

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Radiomics

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Radiomics

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Classification of Chronic Pancreatitis (with Radiomics)

Frøkjær et. Al., Abdominal Radiology (2020) 45:1497–1506

n=77 CP patients and 22 healthy controls (using DWI)

CP: 98% accuracy

Diabetes: 83% accuracy

EPI: 82% accuracy

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Classification of Pancreatic Diseases

After segmentation, region of interest data is fed into the classifier (deep learning) to identify the pathologies

https://www.mdpi.com/2072-6694/14/2/376

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2/17/2025

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Classification of Pancreatic Cancer

Deep learning and radiomics show strong potential for improving pancreatic cancer diagnosis using CT and MRI.

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2024

atirkes@iu.edu

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Future Steps

  • Multimodal Deep Learning

Combination of imaging, clinical, pathological, and other biomarkers

  • Explainable / Trustworthy AI

AI should have reasonings/explanations for their predictions

  • Multicenter trials

AI has generalization problems, one center data-based model may not work in other centers

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Challenges

  • Diagnosis / Prognosis requires explainability

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Challenges

  • Data sharing & Multi-Center Studies --> ethical / privacy issues

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Challenges

  • Data sharing & Multi-Center Studies --> ethical / privacy issues

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Challenges

  • Data sharing & Multi-Center Studies --> ethical / privacy issues
  • IEEE ISBI 2025 (H. Pan et al)

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Dice Jaccard Precision Recall HD95 ASSD

ACC AUC ACC AUC

T1 T2

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Thank you for listening, Questions?

atirkes@iu.edu

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