Can pancreatic Cancer's inflammatory footprint be stopped?
NCT ID NCT07765316
First seen Aug 14, 2026 · Last updated Aug 18, 2026 · Updated 2 times
Summary
This observational study looks at how pancreatic cancer changes immune cells in the blood. Researchers will compare blood samples from 50 people with newly diagnosed, untreated pancreatic cancer to 50 age-matched people with a non-cancerous pancreatic condition. They aim to identify specific immune cell changes driven by tumor-related inflammation, which could reveal new targets for future treatments. Participants with cancer will be followed for 12 months to see if these immune changes relate to their clinical outcomes.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this could identify new drug targets to block cancer-related inflammation and potentially improve future treatments for pancreatic cancer.
- What could go wrong
- This is an observational study, so it won't test any treatment directly. Findings may not lead to immediate therapies, and results might not apply to all patients.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 100 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Sep 2026
An estimate. Start dates often move.
- Expected to finish
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Dec 2029
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
The study population will include adults with newly diagnosed, non-metastatic, treatment-naïve pancreatic ductal adenocarcinoma (PDAC) evaluated at the Pancreatic Surgery Unit of IRCCS Ospedale San Raffaele, and age-matched control patients. Controls will be recruited among patients with intraductal papillary mucinous neoplasm (IPMN) under surveillance at the Pancreatic Cystic Lesion outpatient clinic, with no evidence of pancreatic malignancy at enrollment. Control patients will be selected to match the age of PDAC patients within ±5 years whenever feasible. The study will include 50 PDAC patients and 50 age-matched controls
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria * For all participants: * Age ≥18 years. * Ability and willingness to autonomously provide written informed consent. * For the PDAC cohort: * Clinical diagnosis of non-metastatic pancreatic ductal adenocarcinoma (PDAC). * Treatment-naïve status at the time of blood collection, with no prior chemotherapy, radiotherapy, or immunotherapy for PDAC. * Newly diagnosed non-metastatic pancreatic cancer eligible for multimodal treatment. * Candidate for standard clinical management at IRCCS Ospedale San Raffaele. * For the age-matched control cohort: * Patient followed at the Pancreatic Cystic Lesion outpatient clinic of IRCCS Ospedale San Raffaele. * Diagnosis of intraductal papillary mucinous neoplasm (IPMN) under surveillance, with no evidence of pancreatic malignancy at the time of enrollment. * Age within ±5 years of the corresponding PDAC cohort to allow age-matched comparator analyses. * Exclusion Criteria * For all participants: * Inability to autonomously provide informed consent. * For the PDAC cohort: * Failure to meet the inclusion criteria for the PDAC cohort. * Presence of severe comorbidities that, in the investigator's opinion, may interfere with study participation or interpretation of study results. * Previous systemic anti-cancer treatment for PDAC. * Use of anti-inflammatory drugs, including NSAIDs or immunomodulators. * Events or conditions affecting inflammatory parameters, including acute inflammatory or infectious events such as cholangitis, jaundice, or recent invasive procedures. * Hematologic diseases. * Clinically significant hematological abnormalities that may interfere with immune profiling analyses, as assessed by the investigator. * For the age-matched control cohort: * Any acute or chronic inflammatory condition or ongoing infection. * Any history of cancer or immunological disorders.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
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