Skip to main content
Clinical Trials/NCT02560181
NCT02560181
Active, not recruiting
Not Applicable

Pilot Study of Whole Gland Salvage HDR Prostate Brachytherapy for Locally Recurrent Prostate Cancer

Sunnybrook Health Sciences Centre1 site in 1 country30 target enrollmentAugust 2014

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Prostate Cancer Recurrent
Sponsor
Sunnybrook Health Sciences Centre
Enrollment
30
Locations
1
Primary Endpoint
Acute GI toxicities
Status
Active, not recruiting
Last Updated
last year

Overview

Brief Summary

Radiation therapy is considered a standard treatment option for the management of localized prostate cancer. Among the 20-30% of patients who recur, there is no consensus on the optimal salvage therapy. Salvage options available for isolated local recurrence include; temporary or permanent implantation of radioactive seeds into the prostate, complete removal of the prostate gland, use of low temperatures to treat the disease (cryotherapy), and high frequency ultrasound to treat the disease. There are risks of complications associated with all these treatments, and there is presently no consensus as to which treatment is the best. The aim of this pilot study is to look at the feasibility and toxicities of whole gland salvage treatment of the prostate using temporary implantation of radioactive seeds into the prostate.

Detailed Description

Radiation therapy is considered a standard treatment option for the management of localized prostate cancer. Among the 20-30% of patients who recur, there is no consensus on the optimal salvage therapy. Salvage options available for isolated local recurrence include; temporary or permanent implantation of radioactive seeds into the prostate, complete removal of the prostate gland, use of low temperatures to treat the disease (cryotherapy), and high frequency ultrasound to treat the disease. There are risks of complications associated with all these treatments, and there is presently no consensus as to which treatment is the best. The aim of this pilot study is to look at the feasibility and toxicities of whole gland salvage treatment of the prostate using temporary implantation of radioactive seeds into the prostate. Reports of the efficacy and toxicities of whole gland salvage HDR brachytherapy for local recurrence after external beam radiation therapy are limited to single-institution studies with small sample sizes. Given that our institution has the highest volume of prostate brachytherapy cases in Ontario and that we receive a significant number of referrals from other cancer centres for brachytherapy, this study will aim to add to the literature and help guide salvage therapy practice within our institution.

Registry
clinicaltrials.gov
Start Date
August 2014
End Date
August 30, 2027
Last Updated
last year
Study Type
Interventional
Study Design
Single Group
Sex
Male

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Dr. Hans Chung

Radiation Oncologist

Sunnybrook Health Sciences Centre

Eligibility Criteria

Inclusion Criteria

  • Biopsy confirmed locally recurrent prostate adenocarcinoma \> 30mths after completion of XRT by stereotactic transperineal biopsy
  • Staging T2-weighted, DWI- and DCE- MRI that demonstrates recurrence confined to prostate, and correlates with stereotactic transperineal biopsy
  • Previous external beam radiotherapy for prostate cancer with standard/conventional fractionation (1.8-2.0 Gy per fraction), or moderate hypofractionation (2.4-3.4 Gy per fraction).
  • Staging CT or MRI (abdomen and pelvis) and bone scan are negative for metastases
  • IPSS \< 15
  • Baseline (post XRT) serum PSA \< 10ng/mL
  • Prostate volume as measured by TRUS \< 50cc
  • ECOG performance status 0-1

Exclusion Criteria

  • Disease adjacent to the urethra as visible on MRI
  • Any of the following prior therapies; TURP, radionuclide prostate brachytherapy, prostatectomy or prostatic cryosurgery, HIFU, bilateral orchiectomy, chemotherapy for prostatic carcinoma
  • Evidence of castrate resistance (defined as PSA \> 3ng/mL while testosterone is \< 1.7nmol/L) Patients could have been on combined androgen blockade with initial XRT but are excluded if this was started due to PSA progression

Outcomes

Primary Outcomes

Acute GI toxicities

Time Frame: 3 mths post brachytherapy

Acute GI toxicities using NCI CTCAE v4.0

Acute GU toxicities

Time Frame: 3 moths post brachytherapy

Acute GU toxicities utilizing NCI CTCAE v4.0

Secondary Outcomes

  • Acute GU symptoms(5 years)
  • Late GU symptoms(5 years)
  • Late GU toxicities(5 years)
  • Quality of Life (QoL)(5 years)
  • Biochemical disease free survival(5 years)
  • Late GI toxicities(5 years)

Study Sites (1)

Loading locations...

Similar Trials