CCR2-Targeted Imaging for Pancreatic Cancer
What You Need to Know Before You Apply
What is the purpose of this trial?
This trial aims to improve pancreatic cancer treatment by testing a new imaging agent (64Cu-DOTA-ECLIi) alongside a CCR2-targeted therapy. The goal is to identify patients who will benefit from this therapy, potentially enhancing their quality of life while avoiding unnecessary side effects. The trial includes different groups: one undergoing surgery, another receiving standard chemotherapy, and a third receiving the new CCR2-targeted therapy. Patients with newly diagnosed pancreatic cancer, recurrent cancer, or locally advanced cancer that can be surgically removed might be suitable candidates. As a Phase 1 trial, this research focuses on understanding how the treatment works in people, offering participants the opportunity to be among the first to receive this new therapy.
Will I have to stop taking my current medications?
The trial information does not specify whether you need to stop taking your current medications. It's best to discuss this with the trial coordinators or your doctor.
Is there any evidence suggesting that this trial's treatments are likely to be safe?
Research has shown that the imaging agent 64Cu-DOTA-ECL1i is under study for its ability to detect a protein called CCR2 in pancreatic cancer. This could help monitor changes in the cancer when using treatments targeting CCR2.
Currently, no specific tests exist to select patients for this therapy or to assess their response. Therefore, the imaging agent could become a valuable tool for better treatment planning. However, since this trial is in its early stages, researchers are still learning about the safety of 64Cu-DOTA-ECL1i in humans.
The imaging agent has shown promise in detecting cancer details in lab models, but there is limited information on its tolerability and side effects in people. While there is potential, more research is needed to understand its safety for human use.12345Why are researchers excited about this trial's treatments?
Researchers are excited about these treatments because they employ a novel imaging agent, 64Cu-DOTA-ECL1i, which targets the CCR2 receptor. This approach is different because it allows for precise imaging of pancreatic tumors, potentially improving the accuracy of diagnoses and the monitoring of treatment responses. Unlike traditional options that primarily rely on chemotherapy and surgery without such targeted imaging, this method could help tailor treatments more effectively to individual patients' needs. By providing detailed insights into the tumor environment, researchers hope this technique will lead to better outcomes for patients with pancreatic cancer.
What evidence suggests that this trial's treatments could be effective for pancreatic cancer?
Research has shown that the imaging agent 64Cu-DOTA-ECL1i, which targets CCR2, has potential based on early studies. It effectively detects CCR2, a protein linked to inflammation, in various disease models. In mice, this tracer demonstrated low toxicity and was quickly eliminated by the kidneys, suggesting potential safety for humans. In this trial, participants in Cohort 1a will undergo 64Cu-DOTA-ECL1i-PET/CT imaging after neoadjuvant therapy and surgery, while those in Cohort 1b will receive standard chemotherapy with imaging before and during treatment. Cohort 2 will explore CCR2-targeted therapy with imaging before and after treatment cycles. Although a clinical marker for CCR2-targeted therapy does not yet exist, this imaging agent could identify patients who might benefit from these treatments, which is crucial because some therapies can be highly toxic. The main goal is to use this imaging to guide treatment and improve outcomes for pancreatic cancer patients.13567
Who Is on the Research Team?
Farrokh Dehdashti, M.D.
Principal Investigator
Washington University School of Medicine
Are You a Good Fit for This Trial?
This trial is for adults over 18 with early-stage pancreatic cancer scheduled for surgery, or those who've had chemo and can now have surgery. It's also open to patients with advanced stages eligible for CCR2-targeted therapy. Participants must not be pregnant/nursing and should agree to a pregnancy test if applicable.Inclusion Criteria
Exclusion Criteria
Timeline for a Trial Participant
Screening
Participants are screened for eligibility to participate in the trial
Imaging and Pretherapy Assessment
Participants undergo 64Cu-DOTA-ECL1i-PET/CT imaging to assess CCR2 expression and tumor uptake prior to therapy
Treatment
Participants receive either standard of care chemotherapy or CCR2-targeted therapy, with additional imaging to monitor response
Follow-up
Participants are monitored for safety and effectiveness after treatment, including additional imaging to assess response
What Are the Treatments Tested in This Trial?
Interventions
- 64Cu-DOTA-ECLIi
Find a Clinic Near You
Who Is Running the Clinical Trial?
Washington University School of Medicine
Lead Sponsor
National Cancer Institute (NCI)
Collaborator