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SPORT High-Risk Trial Evaluating SABR in Prostate Cancer

Not Applicable
Active, not recruiting
Conditions
Prostate Cancer
Interventions
Radiation: Stereotatic Radiotherapy
Registration Number
NCT03253978
Lead Sponsor
Belfast Health and Social Care Trust
Brief Summary

The study will examine stereotactic ablative body radiotherapy (SABR), a new technique to deliver radiotherapy to men with prostate cancer. In addition to this, it will look at the effect of SABR on levels of markers of radiation exposure and bowel damage, along with other potential markers of outcome and side effects. Quality of life and any side effects that develop during and after treatment will also be assessed.

Detailed Description

The study will examine stereotactic ablative body radiotherapy (SABR), a new technique to deliver radiotherapy to men with prostate cancer. In addition to this, it will look at the effect of SABR on levels of markers of radiation exposure and bowel damage, along with other potential markers of outcome and side effects. Quality of life and any side effects that develop during and after treatment will also be assessed.

Participants will be treated with five treatments (instead of the standard 37). This is more convenient for them and also allows the treatment of many more people in the same time frame, which should improve the timely delivery of radiotherapy for all patients.

Thirty men with high-risk prostate cancer will be enrolled into the study. They will all be treated with hormone therapy and radiotherapy to the prostate and seminal vesicles. In addition, half of the men will receive an additional dose of radiation to their pelvis. Gold markers will be placed in the prostate before radiotherapy to allow precise targeting of the prostate during treatment. CT scans are taken before and after each treatment to ensure the accuracy of its delivery.

Blood urine and prostate tissue samples will be taken before, during and after radiotherapy. Side effects and quality of life will also by assessed during this time.

Ultimately, this may allow us to predict which men are at increased risk of side effects from radiotherapy and allow closer monitoring, earlier intervention and perhaps alternative treatments in some cases. This should improve the control of prostate cancer and reduce the risk of serious treatment-related side effects

Recruitment & Eligibility

Status
ACTIVE_NOT_RECRUITING
Sex
Male
Target Recruitment
40
Inclusion Criteria

Patients with histologically confirmed prostate adenocarcinoma who elect for radical radiotherapy, with at least one of the following features:

  • clinical stage T3a N0 M0
  • Gleason score 7 (4+3) or above
  • PSA > 20

No evidence of nodal or distant metastatic disease

WHO performance status 0-2

Life expectancy of at least 5 years

Men greater than or equal to 18 years

Ability to understand and willingness to sign a written informed consent document (completed prior to registration and subsequent randomization), along with willingness to co-operate with follow-up

Planned to receive 12-36 months of ADT as part of standard treatment

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Exclusion Criteria

T stage greater than or equal to T3b / T4

Prostate volume > 90cc

Current evidence of:

  • inflammatory bowel disease or other chronic bowel disorder
  • Autoimmune disease
  • Active uncontrolled bacterial, viral or fungal infection
  • Serious uncontrolled concomitant disease
  • Known coagulopathy or bleeding diasthesis
  • Anticoagulation medication (if unsafe to insert for seed insertion)
  • Bilateral hip prosthesis or fixation which would interfere with standard radiation beam configuration
  • Concurrent experimental or cytotoxic drugs
  • Allergy to gold
  • Severe lower urinary tract symptoms - International Prostate Symptom Score (IPSS) > 19
  • Any other contra-indication to hormonal therapy or radical radiotherapy.

History of:

  • Previous major abdominal surgery or history of bowel adhesions
  • Prior pelvic radiotherapy
  • Active malignancy within the preceding five years (other than basal cell carcinoma)

Evidence of:

  • Castrate-resistance (rising PSA with castrate levels of testosterone on LHRHa and anti-androgen)
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Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
SABR to prostate / seminal vesicles with pelvic ENIStereotatic Radiotherapy36.25Gy / 5 fractions to prostate and seminal vesicles with additional SABR (25Gy /5 fractions) delivered to the pelvic nodes.
SABR to prostate and seminal vesicles onlyStereotatic Radiotherapy36.25Gy / 5 fractions to prostate and seminal vesicles.
Primary Outcome Measures
NameTimeMethod
Adequate recruitment rate24 months

adequate recruitment rate (30 patients in 24 months)

Acute toxicity of SABR90 days of completion of SABR

Acute toxicity of SABR (as assessed by CTCAE v4.03 scores until 90 days of completion of SABR)

Quantification of acute toxicity in each treatment groupuntil 90 days post completion of radiotherapy

Quantification of acute toxicity in each treatment group to enable calculation of the sample size for the Phase II RCT (using CTCAE v4.03 scores measured until 90days post completion of radiotherapy)

Number of SABR plans delivered as planned and on schedule29 days (treatment period)

Number of SABR plans delivered as planned and on schedule

Acute quality of life during and after SABR90 days after completion of SABR

Acute quality of life during and after SABR (as assessed by EPIC and IPSS scores until 90 days after completion of SABR)

Secondary Outcome Measures
NameTimeMethod
Overall survivalup to ten years post completion of SABR

Overall survival

Late toxicity of SABRfrom 90 days and up to ten years post completion of SABR

Late toxicity of SABR (as assessed by GI and GU RTOG late toxicity scores from 90 days to ten years post completion of SABR)

Late patient-reported quality of lifeup to ten years post completion of SABR

Late patient-reported quality of life (as assessed by EPIC and IPSS scores from 90 days to ten years post completion of SABR)

Prostate cancer-specific survivalup to ten years post completion of SABR

Prostate cancer-specific survival

Rate of PSA failureup to ten years post completion of SABR

Rate of PSA failure as assessed by Phoenix criteria

Trial Locations

Locations (1)

Belfast Health and Social Care Trust

🇬🇧

Belfast, Co. Antrim, United Kingdom

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