MR-Adaptive Radiation Therapy for Anal Cancer With EScalated-Treatment in a Risk-Optimized Approach
Start Date
9/29/2023
Completion Date
9/1/2028
Summary
The proposed study is a phase II, single arm, open-label trial of MR-guided radiation therapy (RT) with risk stratified RT dose selection in patients with anal cancer. Based on previous data, a risk adaptive treatment approached is proposed in 4 groups: Low risk, standard risk, intermediate risk, and high risk. Human papillomavirus (HPV) DNA will be analyzed to identify novel biomarkers that predict chemoradiotherapy (CRT) response and toxicity.
Detailed Description
After being informed about the study and potential risks, all patients giving written informed consent will undergo a risk-stratified dose of treatment (radiation dose and chemotherapy number of cycles) based on predefined clinical and biological biomarkers for anal squamous cell carcinoma (SCC). Radiotherapy will be delivered on the MR-Linac for image-guided-radiation therapy (IGRT). Patients will be followed for up to 5 years after radiotherapy and be required to complete questionnaires and clinic visits. Patients have the option to complete blood and tissue samples during the study.
Eligibility Criteria
Age Range: 18 years to No maximum
Interventions
Radiotherapy - Low risk group
Radiotherapy - Standard risk group
Radiotherapy - Intermediate risk group
Radiotherapy - High risk group
Conditions
Locations
Allegheny Health Network
Pittsburgh, Pennsylvania 15212
United States
Medical College of Wisconsin Cancer Center
Milwaukee, Wisconsin 53226
United States
Austin Health
Heidelberg, Victoria 3084
Australia
Princess Margaret Cancer Centre
Toronto, Ontario M5G 2C1
Canada
CHUM - Centre hospitalier de l'Université de Montréal
Montreal, Quebec H2X 0C1
Canada