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PET-CT Scans for Head and Neck Cancer
N/A
Recruiting
Led By John J Kim, MD
Research Sponsored by University Health Network, Toronto
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Non-nasopharynx head and neck mucosal squamous cell carcinoma
To be eligible for the second study PET-CT scan: FDG avid tumour (or minimum SUV of 2.5) on the first study PET-CT scan
Must not have
Inability to lie supine for study duration
Prior head and neck radiotherapy
Timeline
Screening 3 weeks
Treatment Varies
Follow Up up to 5 years
Awards & highlights
All Individual Drugs Already Approved
No Placebo-Only Group
Summary
This trial is testing how well PET scans can help plan and give radiation therapy to people with head and neck cancer.
Who is the study for?
This trial is for adults with non-nasopharynx head and neck cancers who haven't had chemotherapy or radiotherapy in the last 5 years. They should have visible cancer that's treatable with radiation alone, and a tumor that shows up on PET scans. Pregnant individuals or those unable to consent are excluded.
What is being tested?
The study is testing how helpful PET scans are before and during radiation treatment for head and neck cancer patients. It aims to improve treatment planning by using additional PET scan data alongside routine tests.
What are the potential side effects?
While the trial focuses on imaging rather than drugs, potential side effects may include discomfort from lying still during the scan, anxiety from being in a confined space, and exposure to low levels of radiation.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
My cancer is a type of squamous cell not in the nasopharynx area.
Select...
My tumor showed high activity on the initial PET-CT scan.
Select...
I am 18 years old or older.
Select...
I have received radiotherapy with the goal of curing my condition.
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
I cannot lie on my back for an extended period.
Select...
I have had radiotherapy for head or neck cancer.
Select...
I have not had chemotherapy or EGFR inhibitors in the last 5 years.
Select...
My cancer has spread to distant parts of my body.
Select...
I have squamous cell carcinoma of the head and neck.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ up to 5 years
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~up to 5 years
Treatment Details
Awards & Highlights
All Individual Drugs Already Approved
Therapies where all constituent drugs have already been approved are likely to have better-understood side effect profiles.
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
1Treatment groups
Experimental Treatment
Group I: HNSCC Patients receiving RTExperimental Treatment1 Intervention
Find a Location
Who is running the clinical trial?
University Health Network, TorontoLead Sponsor
1,521 Previous Clinical Trials
503,284 Total Patients Enrolled
John J Kim, MDPrincipal InvestigatorThe Princess Margaret Cancer Foundation
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I cannot lie on my back for an extended period.My cancer is a type of squamous cell not in the nasopharynx area.I have had radiotherapy for head or neck cancer.My tumor showed high activity on the initial PET-CT scan.I am 18 years old or older.I have not had chemotherapy or EGFR inhibitors in the last 5 years.I have cancer in the upper part of my throat behind the nose.I have received radiotherapy with the goal of curing my condition.I have not had any cancer except for skin cancer in the last 5 years.My cancer has spread to distant parts of my body.I have squamous cell carcinoma of the head and neck.
Research Study Groups:
This trial has the following groups:- Group 1: HNSCC Patients receiving RT
Awards:
This trial has 2 awards, including:- All Individual Drugs Already Approved - Therapies where all constituent drugs have already been approved are likely to have better-understood side effect profiles.
- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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