PET Imaging with 18F-FDG for Cervical Cancer
What You Need to Know Before You Apply
What is the purpose of this trial?
This trial tests whether a special imaging technique can better identify cancerous lymph nodes in the pelvis of women with certain types of cervical or endometrial cancer. By using a radioactive substance called 18F-Fluorodeoxyglucose (18F-FDG) during a PET/CT or PET/MRI scan, researchers aim to see cancer more clearly before surgery. Women diagnosed with stage IB1 cervical cancer or certain high-grade endometrial cancers who are planning for surgery might be suitable candidates. As a Phase 1 trial, the research focuses on understanding how the treatment works in people, offering participants the opportunity to be among the first to receive this innovative imaging technique.
Do I need to stop my current medications for the trial?
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.
What prior data suggests that this imaging technique is safe for cervical cancer patients?
Research has shown that 18F-Fluorodeoxyglucose (18F-FDG) is often used in PET scans to help detect cancer in the body. Studies have found it useful for determining the stage of cervical cancer and planning treatment. This helps doctors understand the extent of cancer spread and decide on the best treatment plan.
Regarding safety, 18F-FDG is generally well-tolerated. Although it is a radioactive substance, only small amounts are used during scans. No specific evidence from these studies indicates negative side effects when injected into the cervix. However, since this study is in its early phase, it primarily focuses on safety, and any risks are closely monitored.
In conclusion, while 18F-FDG is widely used and considered safe for imaging, this trial takes extra precautions to ensure its safety when injected into the cervix for cervical cancer imaging. Participants will be closely monitored for any adverse reactions.12345Why are researchers excited about this trial?
Researchers are excited about using 18F-Fluorodeoxyglucose (18F-FDG) in combination with PET/CT and PET/MRI imaging for cervical cancer because it offers a unique approach to detecting cancerous tissues. Unlike traditional imaging methods, which might not clearly distinguish between healthy and cancerous cells, 18F-FDG highlights cancer cells by targeting their higher glucose uptake, making them stand out more vividly during scans. This targeted approach could potentially lead to more precise staging and treatment planning, allowing doctors to tailor interventions more effectively. Additionally, using advanced imaging techniques like PET/MRI can provide more detailed information about the tumor's structure and activity, which could improve surgical outcomes and overall patient management.
What evidence suggests that PET imaging with 18F-FDG is effective for cervical cancer?
This trial will evaluate the effectiveness of 18F-FDG PET/CT and PET/MRI imaging for cervical cancer. Studies have shown that 18F-FDG PET/CT scans effectively detect cervical cancer, especially in identifying cancer in the lymph nodes near the cervix and uterus. One study found these scans to be 88.7% accurate in predicting primary cervical cancer, with a high ability to both detect cancer and confirm its absence. PET/MRI scans also demonstrate high accuracy and surpass MRI alone in assessing cancer spread. Both types of scans help predict patient response to treatment, making them valuable tools in managing cervical cancer.46789
Who Is on the Research Team?
Jennifer Mueller, MD
Principal Investigator
Memorial Sloan Kettering Cancer Center
Are You a Good Fit for This Trial?
This trial is for women over 18 with stage IB1 cervical cancer or high-grade endometrial cancer, who are fit for surgery and have controlled blood pressure. They must not be pregnant, have a hemoglobin level of at least 10 g/dL, albumin of at least 3 g/dL, glucose under 200 mg/dL, creatinine under 1.6 mg/dL, and no severe health conditions that would interfere with an MRI.Inclusion Criteria
Exclusion Criteria
Timeline for a Trial Participant
Screening
Participants are screened for eligibility to participate in the trial
Pre-surgical Imaging
Participants undergo intracervical 18F-FDG injection during a dynamic PET/CT scan to map lymph nodes before surgery
Surgery and Standard Care
Participants receive standard peri- and postoperative care following the imaging procedure
Follow-up
Participants are monitored for safety and effectiveness after treatment
What Are the Treatments Tested in This Trial?
Interventions
- 18F-Fluorodeoxyglucose (18F-FDG)
- PET/CT imaging
- PET/MRI imaging
Find a Clinic Near You
Who Is Running the Clinical Trial?
Memorial Sloan Kettering Cancer Center
Lead Sponsor