Image processing and analysis for the DCE-MRI was performed using an application for evaluating DCE-MRI (MR Tissue4D) based on commercial software (Syngo.via VB30A, Siemens Healthineers). The perfusion maps were generated using a population-based arterial input function within a sphere-shaped volume of interest containing the entire pancreas and adjacent vessels. Although the software application provided parametric maps based on the Tofts model, we only used measurements from the time–intensity curve. One abdominal radiologist with 12 years of experience in pancreatic MRI performed the image analysis and measured the pancreatic duct diameter in the head, body, and tail of the pancreas. The radiologist also drew six regions of interest (ROIs) in three areas of the vessels (the descending aorta at the left crus level, celiac axis, and superior mesenteric artery (SMA)) and three areas of the pancreas (head, body, and tail). The demarcation of the head, body, and tail of the pancreas was based on the 8th edition of the American Joint Committee on Cancer (AJCC) system [16 ], as follows: the head is to the right of the superior mesenteric–portal vein confluence, the body is between the left border of the superior mesenteric vein and the left border of the aorta, and the tail is between the left border of the aorta and the hilum of the spleen. ROIs in the vessels were free-hand drawn as large as possible while avoiding the vessel wall, and those in the pancreas had sizes larger than 50 mm2. From each ROI, we measured the peak-enhancement time, which is the time between the start of image acquisition and the highest signal intensity. The delay time was based on the time elapsed between the peak-enhancement time in the aorta and the pancreas. The peak concentration in the ROI was recorded from the time–intensity curve.
Quantitative DCE-MRI Analysis of Pancreatic Perfusion
Image processing and analysis for the DCE-MRI was performed using an application for evaluating DCE-MRI (MR Tissue4D) based on commercial software (Syngo.via VB30A, Siemens Healthineers). The perfusion maps were generated using a population-based arterial input function within a sphere-shaped volume of interest containing the entire pancreas and adjacent vessels. Although the software application provided parametric maps based on the Tofts model, we only used measurements from the time–intensity curve. One abdominal radiologist with 12 years of experience in pancreatic MRI performed the image analysis and measured the pancreatic duct diameter in the head, body, and tail of the pancreas. The radiologist also drew six regions of interest (ROIs) in three areas of the vessels (the descending aorta at the left crus level, celiac axis, and superior mesenteric artery (SMA)) and three areas of the pancreas (head, body, and tail). The demarcation of the head, body, and tail of the pancreas was based on the 8th edition of the American Joint Committee on Cancer (AJCC) system [16 ], as follows: the head is to the right of the superior mesenteric–portal vein confluence, the body is between the left border of the superior mesenteric vein and the left border of the aorta, and the tail is between the left border of the aorta and the hilum of the spleen. ROIs in the vessels were free-hand drawn as large as possible while avoiding the vessel wall, and those in the pancreas had sizes larger than 50 mm2. From each ROI, we measured the peak-enhancement time, which is the time between the start of image acquisition and the highest signal intensity. The delay time was based on the time elapsed between the peak-enhancement time in the aorta and the pancreas. The peak concentration in the ROI was recorded from the time–intensity curve.
Corresponding Organization : Catholic University of Korea
Variable analysis
- None explicitly mentioned
- Pancreas edge sharpness
- Motion artifact
- Streak artifact
- Noise
- Overall image quality
- Presence of focal lesion in the pancreas
- Diagnosis for the focal lesion
- Pancreatic duct diameter in the head, body, and tail of the pancreas
- Peak-enhancement time in the vessels (descending aorta at the left crus level, celiac axis, and superior mesenteric artery) and the pancreas (head, body, and tail)
- Delay time between the peak-enhancement time in the aorta and the pancreas
- Peak concentration in the vessels and the pancreas
- None explicitly mentioned
- None mentioned
- None mentioned
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