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High Risk Prostate Cancer clinical trials

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NCT ID: NCT02107287 Completed - Clinical trials for High Risk Prostate Cancer

Hypofractionated Intensity Modulated Radiation Therapy Plus Hormonal Therapy in Patients With High Risk Prostate Cancer

Start date: August 2011
Phase: N/A
Study type: Interventional

Considering the promising results with hypofractionated in low and intermediate risk prostate cancer, our proposal is to translate this experience to patients with high risk prostate cancer. Patients with high risk disease would receive hypofractionated RT to the prostate and to the external and internal iliac lymph nodes using IMRT plus long-term hormonal therapy. The objective of the study is to show that long term grade>2 late toxicity is acceptable and similar to published data using hypofractionated technique in the prostate only.

NCT ID: NCT01695473 Terminated - Clinical trials for High Risk Prostate Cancer

Neoadjuvant BKM120 in High-risk Prostate Cancer

Start date: April 23, 2013
Phase: Phase 2
Study type: Interventional

This is a phase II, study of BKM120 in patients with high-risk, localized prostate cancer. Eligible patients will be enrolled and scheduled to have an ultrasound-guided biopsy of the prostate to confirm high-risk disease and collect prostate tissue for analysis. Two weeks after the biopsy, patients will begin taking 100 mg/day of BKM120. BKM120 will be given at this dose level orally once daily for 14 days prior to radical prostatectomy at University of California, San Francisco. Radical prostatectomy will be performed on the day of the last dose of BKM120 at day 14. No further drug will be tken after the radical prostatectomy.

NCT ID: NCT01488968 Recruiting - Clinical trials for High-risk Prostate Cancer

Conventional Versus Hypofractionated Radiation in High Risk Prostate Patients

CHIRP
Start date: March 2012
Phase: N/A
Study type: Interventional

Hypofractionated regimen in high-risk prostate cancer will allow the investigators to deliver higher biological doses to targets in order to improve tumor control and with acceptable rectal toxicity compared to conventional fractionation.