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Radiation Therapy
Adaptive Radiation Therapy for Genitourinary Cancer (ARTGU Trial)
N/A
Waitlist Available
Led By Peter Chung, 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
Histologic diagnosis of adenocarcinoma of the prostate after radical prostatectomy: Clinical stage pT3, pT4, or pT2 with positive margin; OR, any p-stage with persistently elevated post-operative PSA > 0.05ng/mL; OR, a delayed rise in PSA post-operative
Histologic diagnosis of transitional cell carcinoma of the bladder with intact bladder and: Clinical stage cT2, cT3, cT4, and N0 or N1
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 5 years
Awards & highlights
ARTGU Trial Summary
This trial will use Adaptive Radiation Therapy to account for any shifts in the target volume for prostate or bladder cancer patients who receive pelvic nodal radiotherapy.
Who is the study for?
This trial is for adults with certain stages of bladder or prostate cancer. For bladder cancer, it's those who haven't had their bladder removed and are at stage cT2 to cT4 without distant metastases. Prostate cancer patients must have had surgery already but still show signs of the disease or rising PSA levels. People can't join if they've had previous chemo, pelvic radiation, inflammatory bowel disease, or any evidence of the cancer spreading far.Check my eligibility
What is being tested?
The study tests Adaptive Radiation Therapy (ART) in treating pelvic genitourinary cancers by adjusting treatment plans based on MRI and CBCT scans taken during the first week of radiotherapy. The goal is to see how well ART works for these cancers and monitor its effects over five years using follow-up questionnaires and standard PSA testing.See study design
What are the potential side effects?
While not explicitly listed in your information provided, side effects from radiation therapy generally include fatigue, skin reactions in treated areas, inflammation of organs like the bladder or rectum (radiation cystitis or proctitis), as well as potential long-term changes to bowel and urinary function.
ARTGU Trial Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
My prostate cancer was confirmed after surgery and shows signs of aggressive behavior or rising PSA levels.
Select...
My bladder cancer is at a specific stage and has not spread far.
ARTGU Trial Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 5 years
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~5 years
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Dosimetry
Secondary outcome measures
Biochemical Control in Prostate Patients
Bladder Cancer Patients' Quality of Life Function
Feasibility of the use of Fiducial markers for bladder RT: quality of target delineation using fiducial markers
+3 moreARTGU Trial Design
1Treatment groups
Experimental Treatment
Group I: Adaptive Radiation TherapyExperimental Treatment1 Intervention
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Adaptive Radiation Therapy
2016
N/A
~80
Find a Location
Who is running the clinical trial?
University Health Network, TorontoLead Sponsor
1,468 Previous Clinical Trials
484,490 Total Patients Enrolled
63 Trials studying Prostate Cancer
15,400 Patients Enrolled for Prostate Cancer
Peter Chung, MDPrincipal InvestigatorPrincess Margaret Cancer Centre - University Health Network
3 Previous Clinical Trials
326 Total Patients Enrolled
1 Trials studying Prostate Cancer
17 Patients Enrolled for Prostate Cancer
Media Library
Research Study Groups:
This trial has the following groups:- Group 1: Adaptive Radiation Therapy
Awards:
This trial has 1 awards, including:- 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.
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
Is registration for this research endeavor still open?
"Clinicaltrials.gov states that this trial is currently not recruiting patients, as the last time it was updated on April 7th 2022 predates its initial post date of October 1st 2023. However, there are a multitude of other medical trials in search for participants at present numbering 1038 cases."
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