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Phase II Study of Pencil Beam Scanning Proton Stereotactic Body Radiation Therapy for Prostate Cancer

NCT04842890

Description:

This is a single arm phase II study of image-guided pencil beam scanning proton SBRT (40Gy RBE in 5 fractions delivered every other day) for patients with low- and intermediate-risk prostate cancer. The primary aim is to assess GU/GI toxicity of proton SBRT and compare this to historic outcomes associated with photon-based prostate SBRT. The primary endpoint is 2-year grade 3+ GU/GI toxicity free rate by CTCAE v5.0, which is expected to be ≥95%. Toxicity will be evaluated by the treating radiation oncologist at least once during SBRT, then following SBRT at 1, 3, 6, 12, 18, and 24 months. The treatment will be considered safe if grade 3 or higher GU/GI toxicity free rate at 2 years is >85% (95% rate expected with a 10% non-inferiority margin). The accrual goal is 61 patients over 3 years. To ensure that unexpected significant toxicity is identified, all grade 3 or higher toxicities will be reported to the study PI and the trial will stop accruing if at any point 4 or more patients experience a grade 3 or higher toxicity after completing SBRT. This is felt to be conservative given the vast experience with photon SBRT at this dose with an expected G3+ toxicity of ~5%. Secondary objectives are to examine patient-reported urinary, gastrointestinal, sexual, and financial outcomes using IPSS, EPIC-26, and COST questionnaires at the same follow-up timepoints as above. Baseline measures of these domains will be obtained prior to treatment as well. Clinical outcomes will also be evaluated with PSA measured at each follow-up, as well as prostate MRI and biopsies at 2 years. Patients will be followed for at least 2 years to determine rates of PSA relapse, salvage treatment, development of metastases, death from prostate cancer, and overall survival. A dosimetric comparison will be performed where each patient will be planned for proton and photon SBRT to determine possible advantages of proton SBRT.

Related Conditions:
  • Prostate Carcinoma
Recruiting Status:

Recruiting

Phase:

Phase 2

URL:

https://clinicaltrials.gov/show/NCT04842890

Trial Eligibility

Document

Title

  • Brief Title: Phase II Study of Pencil Beam Scanning Proton Stereotactic Body Radiation Therapy for Prostate Cancer
  • Official Title: Phase II Study of Pencil Beam Scanning Proton Stereotactic Body Radiation Therapy for Prostate Cancer

Clinical Trial IDs

  • ORG STUDY ID: NYPC ERC# 2020-027
  • NCT ID: NCT04842890

Conditions

  • Prostate Cancer

Purpose

This is a single arm phase II study of image-guided pencil beam scanning proton SBRT (40Gy RBE in 5 fractions delivered every other day) for patients with low- and intermediate-risk prostate cancer. The primary aim is to assess GU/GI toxicity of proton SBRT and compare this to historic outcomes associated with photon-based prostate SBRT. The primary endpoint is 2-year grade 3+ GU/GI toxicity free rate by CTCAE v5.0, which is expected to be ≥95%. Toxicity will be evaluated by the treating radiation oncologist at least once during SBRT, then following SBRT at 1, 3, 6, 12, 18, and 24 months. The treatment will be considered safe if grade 3 or higher GU/GI toxicity free rate at 2 years is >85% (95% rate expected with a 10% non-inferiority margin). The accrual goal is 61 patients over 3 years. To ensure that unexpected significant toxicity is identified, all grade 3 or higher toxicities will be reported to the study PI and the trial will stop accruing if at any point 4 or more patients experience a grade 3 or higher toxicity after completing SBRT. This is felt to be conservative given the vast experience with photon SBRT at this dose with an expected G3+ toxicity of ~5%. Secondary objectives are to examine patient-reported urinary, gastrointestinal, sexual, and financial outcomes using IPSS, EPIC-26, and COST questionnaires at the same follow-up timepoints as above. Baseline measures of these domains will be obtained prior to treatment as well. Clinical outcomes will also be evaluated with PSA measured at each follow-up, as well as prostate MRI and biopsies at 2 years. Patients will be followed for at least 2 years to determine rates of PSA relapse, salvage treatment, development of metastases, death from prostate cancer, and overall survival. A dosimetric comparison will be performed where each patient will be planned for proton and photon SBRT to determine possible advantages of proton SBRT.

Trial Arms

NameTypeDescriptionInterventions
Stereotactic body radiation therapy (SBRT) with Pencil Beam Scanning (PBS) proton therapyOther

    Eligibility Criteria

            Inclusion Criteria:

          -  Biopsy-proven NCCN low- or intermediate-risk prostate cancer, which includes patients
             with:

          -  Gleason score ≤7 disease

          -  PSA ≤20 ng/ml

          -  Clinical T1-T2c disease

               -  Note: Patients who only have radiographic evidence of possible or probable T3
                  disease (i.e., extracapsular extension or seminal vesical invasion) will not be
                  excluded.

          -  KPS ≥ 80%

          -  Prostate size as determined on MRI to be < 100 cc. Prostate size can be determined on
             CT scan if MRI is not available.

          -  Male 18 years of age or older

          -  IPSS ≤ 20

          -  Patient must be a candidate for and agree to placement of intraprostatic fiducial
             markers and a hydrogel rectal spacer

          -  Patient must be available for at least 2 years of follow-up

        Exclusion Criteria:

          -  Prior prostate surgery (including cryosurgery)

               -  Note: Patients who underwent TURP or greenlight PVP are eligible if it was > 12
                  weeks prior to the anticipated start date of SBRT

          -  Prior history of chronic prostatitis or urethral stricture

          -  Currently active cancer(s) other than non-melanoma skin cancers. Patients are not
             considered to have currently active cancers if they have completed therapy and are
             considered by their physicians to be at <5% risk of relapse within 2 years.

          -  Life expectancy of < 2 years
    Maximum Eligible Age:N/A
    Minimum Eligible Age:18 Years
    Eligible Gender:Male
    Healthy Volunteers:No

    Primary Outcome Measures

    Measure:1. Grade 3+ GU/GI toxicity-free rate determined by CTCAE v5.0 grading.
    Time Frame:2 years
    Safety Issue:
    Description:The NCI Common Terminology Criteria for Adverse Events v5.0 is a descriptive terminology which can be utilized for Adverse Event (AE) reporting. A grading (severity) scale is provided for each AE term.

    Secondary Outcome Measures

    Measure:1. Patient reported urinary symptoms determined by IPSS.
    Time Frame:2 years
    Safety Issue:
    Description:The International Prostate Symptom Score (IPSS) was developed to assess the severity of lower urinary tract symptoms associated to Benign Prostatic Hyperplasia and has also been applied to other conditions that cause LUTS. The IPSS consists of a total of seven questions that deal with voiding symptoms (incomplete empty, intermittency, weak stream and straining to void) and storage symptoms (frequency, urgency and nocturia) and an additional question to measure quality of life. The score ranges from 0 to 35, with lower scores denoting a better health state.
    Measure:2. Patient reported urinary, bowel, and hormonal quality of life determined by EPIC-26.
    Time Frame:2 years
    Safety Issue:
    Description:EPIC-26 is the "Expanded Prostate Cancer Index Composite" patient reported outcomes questionnaire. A clinical tool to assess urinary, bowel, sexual and vitality health. The score from each of the 5 domains runs from 0 (none) to 12 (severe) impact on quality of life. Each domain score when added together gives an overall score of zero (unaffected) to 60 (severely affected)
    Measure:3. Patient reported financial toxicity determined by COST
    Time Frame:2 years
    Safety Issue:
    Description:Comprehensive Score for Financial Toxicity Functional Assessment of Chronic Illness Therapy (COST-FACIT) was developed as part of a series of questionnaires aimed at measuring different symptom indexes of health-related quality of life in patients with advance disease such as cancer. The survey contains 12 questions and each of them is rated from 0 (not at all) to 4 (very much). This survey focuses on financial distress caused by illness in patients with cancer. It takes about 5 minutes to complete.
    Measure:4. 2-year and 5-year biochemical progression free survival
    Time Frame:2 years and 5 years
    Safety Issue:
    Description:Biochemical failure is defined as a sustained rise in PSA of 2 ng/mL or more above the nadir (the lowest PSA level after radiotherapy).
    Measure:5. 2-year local control determined by MRI and biopsies
    Time Frame:2 years
    Safety Issue:
    Description:
    Measure:6. 2-year and 5-year metastasis free survival
    Time Frame:2 years and 5 years
    Safety Issue:
    Description:
    Measure:7. 2-year and 5-year prostate cancer specific survival
    Time Frame:2 years and 5 years
    Safety Issue:
    Description:
    Measure:8. 2-year and 5-year overall survival
    Time Frame:2 years and 5 years
    Safety Issue:
    Description:
    Measure:9. Dosimetric advantages determined by target coverage, conformality, and normal tissue sparing
    Time Frame:2 years
    Safety Issue:
    Description:

    Details

    Phase:Phase 2
    Primary Purpose:Interventional
    Overall Status:Recruiting
    Lead Sponsor:The New York Proton Center

    Last Updated

    April 13, 2021