Adaptive Radiation Therapy for Cancer
What You Need to Know Before You Apply
What is the purpose of this trial?
This trial explores new ways to use MRI and PET imaging to enhance radiation therapy for certain cancers. It aims to understand how tumors in head and neck cancer and brain metastases resist treatment, potentially causing cancer recurrence or progression. Participants will undergo imaging with 18F-fluoromisonidazole, a special imaging agent, to identify areas that might not respond well to radiation. Individuals with measurable tumors from head and neck squamous cell carcinoma or brain metastases from other cancers may be suitable for this study. As an Early Phase 1 trial, this research focuses on understanding how the treatment works in people, offering participants a chance to contribute to groundbreaking advancements in cancer therapy.
Do I need to stop my current medications for this 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.
Is there any evidence suggesting that this trial's treatments are likely to be safe?
Research has shown that 18F-fluoromisonidazole, the imaging agent used in this trial, has been studied in several projects. These studies suggest it can help monitor low oxygen levels in tumors and changes related to radiation treatment. However, there isn't enough evidence yet to support its regular use for adjusting radiation doses in head and neck cancer.
MRI (Magnetic Resonance Imaging) is generally well-tolerated because it doesn’t use harmful radiation. It is considered safe for ongoing imaging, which is useful for tracking tumor changes over time.
PET (Positron Emission Tomography) is commonly used in cancer care and has proven to be a safe method for guiding radiation treatment. PET scans involve a small amount of radioactive material, but they are widely used because the benefits for diagnosis and treatment planning outweigh the risks.
Overall, these tools are generally safe and have been used in many studies and clinical settings. They are chosen for trials because they provide important information with a low risk of serious side effects.12345Why are researchers excited about this trial's treatments?
Researchers are excited about this trial because it leverages cutting-edge imaging techniques to improve cancer treatment precision. Unlike traditional methods that rely heavily on static imaging, this approach uses 18F-fluoromisonidazole with MRI and PET scans to dynamically assess tumor behavior and response. This could lead to more personalized and effective radiation therapy, potentially improving outcomes for patients with locally advanced squamous cell carcinoma of the head and neck, as well as those with brain metastases. By tailoring treatment in real time, this method could overcome limitations of current standards, offering a promising advancement in cancer care.
What evidence suggests that this trial's treatments could be effective for cancer?
In this trial, participants with locally advanced squamous cell carcinoma of the head and neck or brain metastases will undergo magnetic resonance imaging (MRI) scans and positron emission tomography (PET) scans using the imaging agent 18F-fluoromisonidazole. Research has shown that this special type of scan, called an 18F-fluoromisonidazole PET scan, can help predict the effectiveness of radiation therapy for head-and-neck cancer. This scan identifies low-oxygen areas in tumors, which are often difficult to treat with radiation. Studies have found that detecting these low-oxygen areas before treatment can provide insights into the potential success of the therapy. The scan helps doctors identify tumor parts that might resist treatment, allowing for more effective therapy planning. While promising, further research is needed to confirm these benefits in everyday medical care.13678
Who Is on the Research Team?
Evan Osmundson, MD
Principal Investigator
Vanderbilt University/Ingram Cancer Center
Are You a Good Fit for This Trial?
This trial is for adults with certain head and neck cancers or brain tumors, who can be measured by scans, have a life expectancy over 6 months, and are in good physical condition. They must not be pregnant, agree to use birth control, and able to consent.Inclusion Criteria
Exclusion Criteria
Timeline for a Trial Participant
Screening
Participants are screened for eligibility to participate in the trial
Pre-Treatment Assessment
Participants undergo MRI and PET scans to assess tumor hypoxia using 18F-fluoromisonidazole
Treatment
Participants receive standard of care stereotactic radiosurgery guided by MRI-based markers of tumor hypoxia
Follow-up
Participants are monitored for tumor recurrence, progression, and radiation necrosis post-treatment
Long-term Follow-up
Participants are evaluated for long-term effects of treatment on tumor hypoxia and radiation necrosis
What Are the Treatments Tested in This Trial?
Interventions
- 18F-fluoromisonidazole
- Magnetic Resonance Imaging (MRI)
- Positron Emission Tomography (PET)
Find a Clinic Near You
Who Is Running the Clinical Trial?
Vanderbilt-Ingram Cancer Center
Lead Sponsor
National Institutes of Health (NIH)
Collaborator