Hyperpolarized 13C-Pyruvate MRI for Solid Cancers
What You Need to Know Before You Apply
What is the purpose of this trial?
This trial explores a new imaging method using hyperpolarized 13C-Pyruvate to better visualize solid tumors in the body. The goal is to determine if this imaging can reveal how tumors respond to standard or experimental treatments. It is ideal for individuals with a targeted cancerous lesion in areas like the pelvis, abdomen, or neck that appear clearly in CT or MRI scans. Participants will undergo specialized MR imaging to monitor tumor changes before and after treatment. This approach could be particularly beneficial for those already scheduled to receive standard cancer treatments or investigational therapies. As a Phase 1 trial, the research focuses on understanding how the treatment works in people, offering participants a chance to be among the first to benefit from this innovative approach.
Will I have to stop taking my current medications?
The trial protocol does not specify if you need to stop taking your current medications. However, it does allow the addition of medications to control blood pressure if needed.
What prior data suggests that hyperpolarized 13C-pyruvate MRI is safe for imaging solid cancers?
Studies have shown that hyperpolarized 13C-pyruvate MRI is generally safe for patients with solid tumors. Past research reported no serious side effects directly linked to this imaging method. Participants experienced only mild and temporary side effects, such as slight discomfort during the MRI scan.
As this trial is in its early stages, researchers focus on assessing its safety and effectiveness as a diagnostic tool. However, studies so far suggest it is a promising and safe way to image cancer.12345Why are researchers excited about this trial?
Researchers are excited about hyperpolarized 13C-pyruvate MRI because it offers a new way to look at solid cancers. Unlike traditional imaging techniques that might take longer to show changes, this method can provide real-time insights into how tumors are metabolizing, potentially detecting changes in just days. The use of hyperpolarized 13C-pyruvate allows for a detailed view of the cancer's metabolism, which could help in assessing how well a treatment is working or in detecting cancer early. This innovative approach could lead to more tailored and effective treatment strategies by allowing doctors to monitor the cancer's response more accurately and quickly.
What evidence suggests that hyperpolarized 13C-Pyruvate MRI is effective for solid cancers?
Research has shown that a special type of MRI, called hyperpolarized 13C-pyruvate MRI, can effectively detect and understand cancer. This technique reveals how cancer cells use energy by tracking changes in pyruvate, a key substance in cell metabolism. For instance, shifts in the balance between lactate and pyruvate in cells can indicate tumor activity or severity. Researchers have applied this imaging method to various cancers, including prostate cancer, to learn more about tumor behavior. While primarily used for diagnosis and understanding metabolic changes, it also holds potential for aiding doctors in treatment decisions. Participants in this trial will undergo hyperpolarized 13C-pyruvate MRI as part of either a feasibility run-in or a biomarker cohort to further explore its utility in clinical settings.12467
Who Is on the Research Team?
Robert Bok, MD, PhD
Principal Investigator
University of California, San Francisco
Are You a Good Fit for This Trial?
This trial is for adults with advanced solid tumors who can follow the study plan and have signed consent. They should be fairly active (ECOG 0 or 1), have a tumor at least 1 cm big that's visible on scans, and good kidney function. Pregnant women, those with certain heart conditions, uncontrolled high blood pressure, or metal implants affecting MRI quality cannot join.Inclusion Criteria
Exclusion Criteria
Timeline for a Trial Participant
Screening
Participants are screened for eligibility to participate in the trial
Feasibility Run-In (Phase I/Part A)
Participants undergo MR imaging at a single time point to optimize imaging parameters.
Biomarker Cohort (Phase II/Part B)
Participants undergo paired hyperpolarized pyruvate/metabolic MR imaging at baseline and after approximately 21 days of SOC or investigational therapy.
Follow-up
Participants are monitored for safety and effectiveness after treatment, including adverse events and clinical outcomes.
What Are the Treatments Tested in This Trial?
Interventions
- Hyperpolarized 13C-Pyruvate
Find a Clinic Near You
Who Is Running the Clinical Trial?
Robert Bok, MD, PhD
Lead Sponsor
National Cancer Institute (NCI)
Collaborator
Sigma-Aldrich
Collaborator
National Institute for Biomedical Imaging and Bioengineering (NIBIB)
Collaborator