Overview

This trial is active, not recruiting.

Conditions prostate cancer, cancer of the prostate, prostate neoplasm
Treatment cyberknife radiosurgery
Sponsor Community Cancer Center, Normal, Illinois
Start date January 2008
End date December 2016
Trial size 100 participants
Trial identifier NCT02225262, CK Prostate-01

Summary

The purpose of this study is to determine the effects of CyberKnife radiosurgery in patients with early stage prostate cancer.

The investigators hypothesize that hypofractionated stereotactic radiotherapy via the CyberKnife® can deliver tumor ablating doses of radiation to prostate tumors safely and effectively while sparing the adjacent tissues (rectum, bladder, ureters, urethra, penile bulb, and bowel) from receiving damaging doses of radiation.

United States No locations recruiting
Other Countries No locations recruiting

Study Design

Endpoint classification efficacy study
Intervention model single group assignment
Masking open label
Primary purpose treatment
Arm
(Experimental)
cyberknife radiosurgery CyberKnife
36.25 Gy delivered in 5 fractions of 7.25 Gy per fraction

Primary Outcomes

Measure
Local control rate
time frame: 5-10 years

Secondary Outcomes

Measure
Overall survival
time frame: 5-10 years

Eligibility Criteria

Male participants at least 21 years old.

Inclusion Criteria: - Male Age ≥ 21 - Histologically proven prostate adenocarcinoma - Clinical stage T1b-T2b, N0-Nx, M0-Mx (AJCC 6th Edition) - PSA ≤ 20 ng/ml - Prostate volume ≤ 100 cc Patients belonging in one of the following risk groups: - Low: - CS T1b-T2a and Gleason 2-6 and PSA ≤ 10 - Intermediate: - CS T2b and Gleason 2-6 and PSA ≤ 10, OR - CS T1b-T2b, and Gleason 2-6 and PSA ≤ 20 ng/ml OR Gleason 7 and PSA ≤ 10 ng/ml Exclusion Criteria: - Any histology other than adenocarcinoma - Age < 21 - KPS <= 40 <70 - ECOG Performance Status ≥ 2 - Patient weight >350 lbs. (table limitation) - Prior XRT to prostate or lower pelvis - Prior surgery or cryotherapy to prostate - Implanted hardware or other material that would prohibit appropriate treatment planning or treatment delivery, in the investigator's opinion - Chemotherapy for a malignancy in the last 5 years - History of an invasive malignancy (other than this prostate cancer, or basal or squamous skin cancers) in the last 5 years - Hormone ablation for 2 months prior to enrollment, or during treatment

Additional Information

Official title Prospective Evaluation of CyberKnife Stereotactic Radiosurgery for Low and Intermediate Risk Prostate Cancer: Emulating Homogenous Dose Distribution
Principal investigator Shermian Woodhouse, MD
Description The CyberKnife system is a type of radiation machine that uses a special system to precisely focus large doses of x-rays (radiation) on the tumor. The device is designed to concentrate large doses of radiation onto the tumor so that injury from radiation to the nearby normal tissue will be minimal.
Trial information was received from ClinicalTrials.gov and was last updated in August 2014.
Information provided to ClinicalTrials.gov by Community Cancer Center, Normal, Illinois.