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CyberKnife Radiosurgery for Locally Recurrent Prostate CA

VIRTUAL HDR CYBERKNIFE RADIOSURGERY FOR LOCALLY RECURRENT PROSTATIC CARCINOMA: A PHASE II STUDY

Status
UNKNOWN
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00851916
Enrollment
20
Registered
2009-02-26
Start date
2009-02-28
Completion date
Unknown
Last updated
2017-07-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Recurrent Prostate Cancer

Brief summary

The purpose of this study is to scientifically evaluate the effects (good and bad) of a new type of radiation treatment in patients with locally recurrent prostate cancer after prior radiotherapy. The treatment is known as prostate radiosurgery, and is distinguished from traditional radiotherapy by the application of smaller, more precisely controlled margins around the area targeted for full dose radiation, and far fewer treatments, using a much larger dose per treatment. This research is being done to see what advantages, if any, prostate radiosurgery may have over other salvage treatment methods, including brachytherapy, cryosurgery, high intensity focused ultrasound (HIFU), hormonal therapy and radical prostatectomy.

Interventions

CyberKnife Radiosurgery

Sponsors

CyberKnife Centers of San Diego
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
MALE
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Histologically confirmed recurrent adenocarcinoma of the prostate, clinical stage T1 - T3 (AJCC 6th Edition, see Appendix II), NX/N0, M0, following prior prostate radiotherapy. * Karnofsky performance status \>80. * Greater than 5 year life expectancy * Greater than 2 years since the original course of radiotherapy. * Absence of distant metastases by radiologic or pathologic assessment. * Absence of lymph node involvement by radiologic or pathologic assessment. * Patients must sign a study-specific informed consent form prior to study entry.

Exclusion criteria

* Stage T4 disease (AJCC 6th Edition, see Appendix II). * Less than 2 years since the original course of radiotherapy. * Lymph node involvement (N1). * Evidence of distant metastases (M1). * Radical surgery for carcinoma of the prostate * Previous or concurrent cancers other than basal, in situ, or squamous cell skin cancers unless disease-free for ≥ 5 years. * Major medical or psychiatric illness, which in the investigator's opinion, would prevent completion of treatment and would interfere with follow-up. * History of inflammatory bowel disease * Late GI or GU Morbidity \> Grade 1 from the prior course of radiotherapy

Design outcomes

Primary

MeasureTime frame
Establish pattern of PSA declinePost CyberKnife Radiosurgery - 5 year f/up

Secondary

MeasureTime frame
Quality of Life realitive to other commonly used radiation treatment methods for recurrent prostate cancerPost CyberKnife Radiosurgery/5 yr. f/up

Countries

United States

Contacts

Primary ContactCarlyn Tripp
ctripp@rmgmed.com619-230-0400

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026