Intensity Modulated Radiation Therapy - Prostate Cancer
Launched by UNIVERSITY HEALTH NETWORK, TORONTO · Sep 12, 2005
Trial Information
Current as of April 28, 2025
Completed
Keywords
ClinConnect Summary
No description provided
Gender
MALE
Eligibility criteria
- Inclusion Criteria:
- • Histologic diagnosis of adenocarcinoma of the prostate within six months of entry
- • Clinical stage T1B, T1C, T2A-C NX MO (see Appendix 1 for staging). Any Gleason score is eligible for entry, but Gleason score must be determined.
- • Patients with a PSA \>10.0 and Gleason score of 7; or patients with any PSA value and Gleason score of \>8 must have clinically negative lymph nodes as determined by a pelvic CT scan done within 12 weeks of entry. A negative bone scan is required before entry for all patients with Gleason score \>8, or any patient with a Gleason score of 7, and a PSA \>10.
- • The patient must not have received any cytotoxic anticancer therapy. Previous or concurrent hormonal therapy for local disease is acceptable.
- • ECOG performance status of 1 or less
- • Age 80 years old or less
- • Serum PSA \<25 ng/ml within 4 weeks of study entry
- • Informed consent
- Exclusion Criteria:
- • Patients with history of inflammatory bowel disease or other contraindication to radical radiation therapy
- • Patients with prior colorectal surgery
- • Any prior pelvic radiotherapy. Any prior TURP done \<12 weeks from study entry.
- • Any previous cytotoxic chemotherapy
- • Patients with prior malignancy except non-melanoma skin carcinoma within 5 years of the diagnosis of prostate cancer
About University Health Network, Toronto
University Health Network (UHN), based in Toronto, is a leading academic health sciences center dedicated to advancing patient care through innovative research and education. As a prominent sponsor of clinical trials, UHN integrates cutting-edge scientific discoveries with clinical practice, facilitating the development of new therapies and treatment modalities. With a commitment to improving health outcomes, UHN collaborates with a diverse network of researchers, healthcare professionals, and industry partners, fostering an environment that prioritizes patient safety and ethical standards in clinical research. Through its extensive resources and expertise, UHN plays a pivotal role in transforming healthcare and enhancing the quality of life for patients both locally and globally.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Toronto, Ontario, Canada
Patients applied
Trial Officials
Charles Catton, MD
Principal Investigator
Princess Margaret Hospital, Canada
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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