Low Dose Supplemental External Radiation With Pd-103 Versus Pd-103 Alone for Prostate Cancer

Phase 3

Completed

• Conditions: Prostate Cancer
• Interventions: Procedure: External beam radiation; Procedure: Pd-103

• Registration Number: NCT00241384
• Lead Sponsor: Schiffler Cancer Center

Brief Summary

The primary purpose of this study is to evaluate two treatment regimens for prostate cancer, prostate implant with 20 Gy of external beam radiation therapy versus prostate implant with 0 Gy of external beam radiation therapy. Patients diagnosed with intermediate risk prostate cancer between the ages of 40 and 80 who have chosen brachytherapy with or without external beam radiation therapy as their intended treatment will be eligible and will be offered participation.

Detailed Description

Approximately 250,000 men are currently diagnosed with prostatic cancer in the United States each year. Of those, 70% have stage T1 or T2 disease (apparently limited to the prostate gland). Clinically localized prostate cancer is a spectrum of disease, ranging from good prognosis to poor prognosis. Patients with a PSA above 10 ng/ml or Gleason score of 7 to 10 are referred to as intermediate risk, with approximately an 80% chance of cure.

Implantation of radioactive sources directly into the prostate (brachytherapy) delivers a high, localized radiation dose while sparing most the of the bladder and rectum. Brachytherapy is well established for other tumor sites, and has become a standard treatment for prostate cancer.

Establishing that a good quality implant alone is as effective as implant plus beam radiation will allow us to routinely drop the use of beam radiation, a change in policy that will decrease the risk of some complications, will be more convenient for patients, and will lower treatment costs.

Study Timeline

• Study Start: 2005-01
• Study First Submitted: 2005-10-14
• Study First Submitted QC: 2005-10-14
• Study First Posted: 2005-10-18
• Status Verified: 2015-11
• Primary Completion: 2015-11
• Study Completion: 2015-11
• Last Update Submitted: 2015-11-16
• Last Update Posted: 2015-11-17

Recruitment & Eligibility

• Status: COMPLETED
• Sex: Male
• Target Recruitment: 396

Inclusion Criteria

• Patients with previously untreated prostatic cancer.
• Must have PSA 10-20 ng/ml, Gleason 7 to 9

Exclusion Criteria

• Patients with proven regional lymph node involvement will be excluded.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Pd-103 with 20Gy External Beam	External beam radiation	Pd-103 with 20Gy External Beam
Pd-103 alone	Pd-103	Pd-103 alone

Primary Outcome Measures

Name	Time	Method
Serial PSA : 6, 12, 18 and 24 months and then yearly.	6, 12, 18 and 24 months and then yearly	Serial PSA : 6, 12, 18 and 24 months and then yearly.
PSA which is suggestive of residual tumor.	as needed	PSA which is suggestive of residual tumor.
Post treatment biopsies in those with persistently elevated	as needed	Post treatment biopsies in those with persistently elevated

Trial Locations

Locations (2)

Veterans Administration Puget Sound Health Care System; 🇺🇸 Seattle, Washington, United States

Schiffler Cancer Center; 🇺🇸 Wheeling, West Virginia, United States