Hemiablative Focal Brachytherapy Pilot Study

St George Hospital

Status and phase: Enrolling; Phase 2

Conditions: Prostate Cancer

Treatments: Radiation: Transperineal template guided mapping biopsy, multiparametric MRI, Hemiablative Focal Brachytherapy

Study type: Interventional

Funder types: Other

Identifiers

NCT02643511

STGAF

Details and patient eligibility

About

Whole gland LDR brachytherapy has been a well established modality of treating low risk prostate cancer. Treatment in a focal manner has the advantages of reduced toxicity to surrounding organs.

AIM: To determine the utility of focal LDR brachytherapy in form of hemiablative treatment for localized prostate cancer demonstrating the feasibility of the delivery of the prescription dose to the half of the prostate in terms of meeting standard dosimetric parameters while respecting same or lower tolerance doses of adjacent normal organs.

To determine acute and late rectal, urinary and sexual toxicity after this procedure.

To assess the change from baseline in QOL indicators at specific time intervals using validated international questionnaires [International Prostate Symptom Score ( IPSS), International Index of Erectile Function ( IIEF ), Expanded Prostate Cancer Index (EPIC)] after this treatment.

To evaluate the local tumour control in terms of biopsy outcomes after focal brachytherapy 36 months after the treatment.

To compare target coverage and relative doses to the rectum and the urethra for the same patient performing a hemigland treatment planning vs Whole gland treatment planning.

STUDY DESIGN: Multi-institution prospective trial to determine whether hemiablative treatment with LDR for prostate cancer is dosimetrically safe and feasible.This study will record data for 20 patients with ipsilateral with low and low tier intermediate risk disease.The study will record quality of life parameters in particular in terms of urinary, rectal and sexual function side effects.

INTERVENTION:

• Baseline Transperineal Template guided mapping prostate biopsy with >20 cores (not required if already performed)
• Multiparametric MRI within the 3 months prior to registration and at 18 & 36 months.
• Hemigland prostate region will be targeted with the prescription dose and receive 144 Gy of Iodine125 (I125).
• The quality of life assessment will focus on erectile function, urinary function, bowel function, and general health related quality of life
• Postimplant CT Planning day 30 after the implant for quality assurance.

MEASUREMENT OF ENDPOINTS :

Dosimetric parameters record, Toxicity and QOL evaluation forms, PSA follow up and biopsies at 36 months to assess local control.

Enrollment: 20 estimated patients

Sex: Male

Ages: 60+ years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• 1. Patients must have histologically proven adenocarcinoma of the prostate.

  2. Patients must have low or low-tier intermediate prostate cancer

  • Low risk prostate cancer patients must have:

    • Clinical stage ≤ T2a,
    • Gleason score =6 and iPSA ≤ 10 ng/ml
    • < 25% cores positive, < 50 % cancer in each core involved

  • Low tier Intermediate risk patients may have:

    • Clinical stageT2a

    • Gleason score ≤ 3+4=7

    • PSA ≤ 10 ng/ml

    • < 25% cores positive, < 50 % cancer in each core

      3. Patients must be fit for general anesthetic. 4. Patients must have unilateral disease on biopsy 5. Patients must have an Eastern Cooperative Oncology Group (ECOG) performance status of 0 - 2.

      4. Men ≥ 65 years of age with a life expectancy estimated to be >10 years. 7. Patients must have no contraindications to interstitial prostate brachytherapy.

      5. Patients on anticoagulant therapy must be able to stop therapy safely for at least 7 days.

      6. Patients must not have any contraindications to MRI 10. IPSS <=16

Exclusion criteria

1. Does not meet staging criteria for low risk or low tier intermediate risk prostate cancer
2. Bilateral prostatic disease
3. Prior hormonal therapy
4. Prior Transurethral resection or middle lobe resection
5. Recent IPSS>
6. Unfit for general anesthetic
7. MRI contraindicated
8. Unable to cease anticoagulant therapy
9. Life expectancy < 10 years
10. IPSS>16

Trial design

Primary purpose: Treatment

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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20 participants in 1 patient group

Prostate biopsy,Hemiablative focal Brachytherapy

Experimental group

Description:

This is a non-randomized, Phase II study examining the efficacy in terms of postimplant dosimetry (primary endpoint) as well as the secondary endpoints of QOL changes, toxicity, local control with post-treatment biopsy outcomes and comparison with historical whole-gland cohorts in men with early stage low volume prostate cancer treated with hemiablative focal brachytherapy

Treatment:

Radiation: Transperineal template guided mapping biopsy, multiparametric MRI, Hemiablative Focal Brachytherapy