Pancreatic Cancer Clinical Trial
Official title:
MRI With Secretin Enhancement to Increase Conspicuity of Pancreatic Cancer
The aim of the study is to evaluate the utility of secretin-enhanced MRI (S-MRI) in detecting and measuring pancreatic lesions in patients with known adenocarcinoma or Intraductal papillary mucinous neoplasm (IPMN) lesions. The hypothesis is that S-MRI is superior to MRI without secretin enhancement (N-MRI) in increasing tumor conspicuity, allowing for improved identification and more accurate measurement of lesions or precursor lesions in the pancreas.
Pancreatic cancer remains the fourth leading cause of cancer-related death in the United
States and is marked by advanced stage at diagnosis and a high mortality rate. Intraductal
papillary mucinous neoplasm (IPMN) is a cystic lesion that can be potentially cancerous,
leading to pancreatic adenocarcinoma. Currently, there is no existing imaging modality that
is both sensitive and cost-effective enough in accurately measuring or detecting
adenocarcinoma and IPMN. Improving the methods used in identification and localization of
this disease is critical.
Secretin, a hormone produced by duodenal mucosal cells increases blood-flow to the pancreas.
The investigators' hypothesis is that as secretin increases blood flow to the pancreas,
there will be increased conspicuity in areas of dysplasia/cancer where there is minimal
blood-flow, enhancing tumor detection. The investigators are conducting a prospective,
randomized-control pilot study of thirty subjects with IPMN or pancreatic cancer who are
undergoing surgical resection at Columbia University's Pancreas Center. Fifteen subjects
will be randomly selected to undergo S-MRI prior to surgery and fifteen subjects will be
selected as controls, undergoing MRI without secretin-enhancement and matched for age, sex,
race and tumor-type. The investigators will first evaluate if secretin allows for increased
tumor conspicuity, enhanced visualization of the lesion, by comparing the calculated tumor
conspicuity of S-MRI to N-MRI groups.
The investigators will then assess if S-MRI imaging allows for increased accuracy in lesion
measurements by looking at the concordance in measurements between S-MRI and tumor specimens
post-resection as compared to the concordance in measurements between N-MRI and tumor
specimens post-resection.
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Allocation: Randomized, Endpoint Classification: Safety Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Diagnostic
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