This phase II trial investigates whether proton radiation therapy directed to the prostate tumor and nearby lymph nodes, is an effective way to treat patients with high-risk prostate cancer who are receiving radiation therapy, and if it will result in fewer gastrointestinal and genitourinary side effects. Proton beam therapy is a new type of radiotherapy that directs multiple beams of protons (positively charged subatomic particles) at the tumor target, where they deposit the bulk of their energy with essentially no residual radiation beyond the tumor. By reducing the exposure of the healthy tissues and organs to radiation in the treatment of prostate cancer, proton therapy has the potential to better spare healthy tissue and reduce the side effects of radiation therapy. The information learned from this study may also help researchers to learn more about proton therapy for the treatment of patients with prostate cancer.
Study sponsor and potential other locations can be found on ClinicalTrials.gov for NCT04725903.
Locations matching your search criteria
United States
Georgia
Atlanta
Emory University Hospital/Winship Cancer InstituteStatus: Active
Contact: Pretesh Ramanlal Patel
Phone: 404-778-3473
Emory University Hospital MidtownStatus: Active
Contact: Pretesh Ramanlal Patel
Emory Proton Therapy CenterStatus: Active
Contact: Pretesh Ramanlal Patel
PRIMARY OBJECTIVE:
I. To determine the rate of acute grade 2+ gastrointestinal toxicity compared to historical photon treatments.
SECONDARY OBJECTIVES:
I. To determine the rate of acute grade 2+ genitourinary toxicity compared to historical photon treatments.
II. To assess the feasibility of extended-field proton irradiation of high-risk prostate.
III. To demonstrate safety of proton therapy followed by high dose rate (HDR) boost.
IV. To determine patient-reported outcomes (PROs) of toxicity.
OUTLINE:
Patients undergo pelvic proton beam therapy daily on Monday-Friday for 7-9 weeks and then undergo intensity-modulated proton therapy (IMPT). Patients may receive a high-dose rate brachytherapy boost. Patients also undergo collection of blood samples at screening and during follow up, may undergo bone scan, positron emission tomography (PET) and digital rectal exam (DRE) at screening, and undergo computed tomography (CT) or magnetic resonance imaging (MRI) at screening and then as clinically indicated.
After completion of study treatment, patients are followed up at 1, 3, 6, 9 and 12 months, and 1, 1.5, 2, 2.5, and 3 years.
Lead OrganizationEmory University Hospital/Winship Cancer Institute
Principal InvestigatorPretesh Ramanlal Patel