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Focal Salvage HDR Brachytherapy for the Treatment of Prostate Cancer

Pilot Study of Focal Salvage HDR Prostate Brachytherapy

Status
Active, not recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01583920
Enrollment
60
Registered
2012-04-24
Start date
2012-07-31
Completion date
2028-07-31
Last updated
2024-11-27

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

Conditions

Prostate Cancer

Keywords

prostatic neoplasms, brachytherapy, salvage therapy, recurrent prostate cancer

Brief summary

Radiation therapy is considered a standard treatment option for the management of localized prostate cancer. Among the 20-30% who recur, a proportion of them will present with an isolated local recurrence, meaning no distant metastases. If left untreated, it may serve as a source for subsequent metastases. 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, 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. Therefore, the aim of this pilot study is to look at the feasibility and toxicities of focal treatment of the prostate using temporary implantation of radioactive seeds into the prostate which the investigators hope will be less since the entire prostate is not treated.

Interventions

RADIATIONfocal salvage HDR prostate brachytherapy

Treatment will be delivered using 192-Ir HDR afterloading. Dose prescription is 2 fractions of 13.5 Gy each, delivered 1 week apart.

Sponsors

Canadian Association of Radiation Oncology
CollaboratorINDUSTRY
Sunnybrook Health Sciences Centre
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

* Biopsy-confirmed locally recurrent prostate adenocarcinoma \> 30months after the completion of XRT, SBRT, LDR or HDR brachytherapy boost with XRT, or LDR or HDR brachytherapy as monotherapy by a stereotactic transperineal biopsy * Staging T2-weighted, DWI and DCE-MRI that demonstrates solitary recurrence confined to prostate, and correlates with stereotactic transperineal biopsy * Staging CT or MRI (abdomen and pelvis) and bone scan are negative for metastases * American Urological Association Symptom Index Score (ie. IPSS) \< 15 * Baseline (post-XRT) serum PSA \< 10 ng/mL * Prostate volume as measured by transrectal ultrasound (TRUS) \< 50cc * ECOG performance status 0-1

Exclusion criteria

* Any of the following prior therapies: transurethral resection of the prostate (TURP), radionuclide (permanent or temporary implantation) prostate brachytherapy, prostatectomy or prostatic cryosurgery, HIFU (high-intensity focused ultrasound), bilateral orchiectomy, chemotherapy for prostatic carcinoma * Evidence of castrate resistance (defined as PSA \> 3 ng/mL while testosterone is \< 1.7 nmol/L). Patients could have been on combined androgen blockade with initial radiotherapy but are excluded if this was started due to PSA progression.

Design outcomes

Primary

MeasureTime frameDescription
Incidence of acute urinary and rectal toxicitiesAcute period (<6 months)Common Terminology Criteria for Adverse Events (CTCAE) v4.0

Secondary

MeasureTime frameDescription
Incidence of late urinary and rectal toxicitiesLate period (>6 months)Common Terminology Criteria for Adverse Events (CTCAE) v4.0
Biochemical (ie. prostate specific antigen) disease free survival5 years
Quality of Life (QoL)5 yearsExpanded Prostate Cancer Index Composite (EPIC)
Acute and late urinary toxicities5 yearsAmerican Urological Association Symptom Index Score (i.e. IPSS)

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 8, 2026