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HDR Brachytherapy vs SABR in Early-intermediate Prostate Cancer

Not Applicable
Recruiting
Conditions
Biochemical Relapse Free Survival
Complications Rates (Erectile Dysfunction, GI, GU Complications)
Interventions
Radiation: Stereotactic ablative radiotherapy
Radiation: High dose rate brachytherapy
Registration Number
NCT04870567
Lead Sponsor
N.N. Petrov National Medical Research Center of Oncology
Brief Summary

This is single center prospective phase 2 randomized trial aiming to compare biochemical and clinical relapse free survival and toxicity profiles of stereotactic body radiotherapy (SBRT) versus high dose rate brachytherapy (HDRB) for localized low- and intermediate risk prostate cancer patients.

Detailed Description

Before SBRT three fiducial markers are obligatory inserted into the prostate. Simulation and every SBRT sessions are performed after bowel preparation (enema) and bladder filling (400ml).Planning MRI on diagnostic table with subsequent fusing with simulation CT is obligatory. The clinical target volume (CTV) include the prostate only (low-risk patients) or prostate and proximal 1/3 of seminal vesicles (intermediate-risk patients). CTV to planning target volume (PTV) expansion was 3-5 mm in all direction except posteriorly (in the direction of the rectum) where it is 1-3 mm. Dose must be delivered as 5 fraction of 7.25Gy. V100% for PTV ≥ 95%. Main dose constraints are as follows: D 2cm³ ≤ 36Gy for rectum (below 75Gy EQD2)., V 37.5 Gy \<5 cm³ for bladder, V 20 Gy \<10 cm³ for femoral heads. Androgen deprivation therapy is not permitted.

All treatments must be performed on conventional linear accelerators with cone beam CT guidance before each fraction, intrafractional motion monitoring is optional.

After spinal anesthesia steel or plastic needle placement performed under TRUS guidance. Pre- and post-insertion ultrasound based planning is obligatory in all cases. Two fractions of 13Gy are delivered with 2 separate implantations and 2-3 weeks interval. The CTV was defined as the prostate capsule with 1mm (low-risk) - 3 mm (intermediate risk) expansion plus proximal 1/3 of seminal vesicles. The PTV was equal to CTV. The rectum, bladder and urethra are contoured as organs at risk. The dosimetry plan objectives are the following: prostate D90 - above 104% and V100% - above 92%; urethra D10 \< 110% , rectum D2cc\<75% (below 75Gy EQD2).

Patients are assessed during treatment, 4-12 weeks after the end of the treatment, every 3 months for the first year and then every 6 months till the end of the study. Normal tissue adverse events are reported according to Common Terminology Criteria for Adverse Events (CTCAE version 5.0). International prostate symptoms score (IPSS) and international index of erectile function (IIEF-5) must be assessed on each visit, maximal urinary rate and residual urine volume - annually.

Recruitment & Eligibility

Status
RECRUITING
Sex
Male
Target Recruitment
350
Inclusion Criteria
  • WHO performance status of 0-2,
  • histologically confirmed prostate adenocarcinoma: Gleason score - 6-7 (4+3), clinical stage T1c-T2c, N0, M0
  • T and N stage determined by clinical examinations, MRI and/or PET-CT with PSMA
  • PSA below 20 ng/ml within the last 30 days
  • international prostate index score (IPSS) below 16
  • medically fit to spinal anesthesia
  • prostate volume below 110 cm³
  • maximal urinary rate above 9 ml/sec, residual urine volume below 30ml,
  • in the case of previous transurethral resection interval of at least 9 months after procedure.
Exclusion Criteria
  • stage T3-T4,
  • PSA > 20 ng/ml,
  • clinically detected lymph node or distant metastases,
  • previous pelvic irradiation,
  • rectal surgery.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Stereotactic ablative radiotherapyStereotactic ablative radiotherapyBefore SBRT three fiducial markers are obligatory inserted into the prostate.Planning MRI on diagnostic table with subsequent fusing with simulation CT is obligatory. CTV to planning target volume (PTV) expansion was 3-5 mm in all direction except posteriorly (in the direction of the rectum) where it is 1-3 mm. Dose must be delivered as 5 fraction of 7.25Gy. V100% for PTV ≥ 95%. Main dose constraints are as follows: D 2cm³ ≤ 36Gy for rectum (below 75Gy EQD2)., V 37.5 Gy \<5 cm³ for bladder, V 20 Gy \<10 cm³ for femoral heads. Androgen deprivation therapy is not permitted. All treatments must be performed on conventional linear accelerators with cone beam CT guidance before each fraction, intrafractional motion monitoring is optional.
High dose rate brachytherapyHigh dose rate brachytherapyAfter spinal anesthesia steel or plastic needle placement performed under TRUS guidance. Pre- and post-insertion ultrasound based planning is obligatory in all cases. Two fractions of 13Gy are delivered with 2 separate implantations and 2-3 weeks interval. The CTV was defined as the prostate capsule with 1mm (low-risk) - 3 mm (intermediate risk) expansion plus proximal 1/3 of seminal vesicles. The PTV was equal to CTV. The rectum, bladder and urethra are contoured as organs at risk. The dosimetry plan objectives are the following: prostate D90 - above 104% and V100% - above 92%; urethra D10 \< 110% , rectum D2cc\<75% (below 75Gy EQD2).
Primary Outcome Measures
NameTimeMethod
Change in the proportion of patients with moderate and severe erectile dysfunction3, 6, 12, 18, 24 and every 6 months through 5 years

Assessed by International Index of Erectile Function (IIEF)

Number of grade 3-5 Adverse Events Assessed by Common Terminology Criteria for Adverse Events CTCAE v55 years after treatment

To evaluate frequency of grade 3-5 toxicity in patients treated by high dose rate brachutherapy (arm 1) and stereotactic ablative radiotherapy (arm 2)

Secondary Outcome Measures
NameTimeMethod
Biochemical relapse free survival5 years after treatment

PSA levels in the blood. Reccurence - nadir + 2 ng/ml

Trial Locations

Locations (1)

Sergey Novikov

🇷🇺

St Petersburg, Russian Federation

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