Hyperpolarized C Pyruvate Magnetic Resonance Imaging, and Blood-Based Biomarkers for Early Detection of Pancreatic Adenocarcinoma in Patients With Intraductal Papillary Mucinous Neoplasms

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorMemorial Sloan Kettering Cancer Center

About this trial

The purpose of this study is for researchers to find ways of detecting pancreatic ductal adenocarcinoma/PDAC early to avoid the invasive procedure of surgery. The study researchers think a combination of imaging and a series of blood tests may be an effective way to detect PDAC early. In this study, researchers will look at whether a combination of the following types of imaging with blood tests can detect PDAC in pancreatic cysts:

* The ImmunoPET scan (immune-positron emission tomography scan) with the imaging agent 89Zr-DFO-HuMab-5B1 * The HP MRI scan (hyperpolarized pyruvate magnetic resonance imaging scan)

Eligibility criteria

Qualifiers

Men and women aged >18 years

Pancreatic cystic neoplasm deemed to be high risk and requiring surgical resection

Able to provide informed consent

Disqualifiers

Pathologic evidence of pancreatic cancer

Pregnant or breast-feeding patients

Refusal or inability to tolerate scan (eg anxiety or claustrophobia)

Inability to lay flat or meet the standard requirements of traditional MRI

Trial design

Treatments tested in this trial

  • 89Zr-DFO-HuMab-5B1 immunoPET
  • HP MRI
  • Blood assay

Treatment groups

25 Participants
are divided into 1 treatment group