ADT and SBRT vs SBRT Alone for Unfavorable Intermediate Risk Prostate Cancer

Clinicaltrials.gov ID: NCT06397703
db-list-check Status RECRUITING
b-loader Phase PHASE3
b-people Age ≥ 18 Years
b-bullseye-arrow Enrollments 392

Conditions

Prostate Cancer

Drugs

Leuprolide, Degarelix or Relugolix

Summary

For this proposed Phase III study, unfavorable intermediate risk prostate cancer patients will be randomized to receive 6 months of Androgen Deprivation Therapy (ADT) in conjunction with stereotactic body radiation therapy/radiosurgery (SBRT) directed to the prostate versus SBRT alone. The patient population will include those with National Comprehensive Cancer Network (NCCN)-defined unfavorable intermediate risk disease. All patients will be followed every 6 months for up to 5 years from the first patient randomized and will undergo a routine 24-30 months post-SBRT prostate biopsy to assess for local tumor control.

Locations

1 location Found with status Recruiting

Status

  • RECRUITING

Central Contacts

Principal Investigator

  • Michael Zelefsky

Eligibility Criteria

Inclusion Criteria:

* Biopsy proven unfavorable intermediate risk prostate cancer, which includes patients with any one of the following variables: Gleason 4+3 disease; Percent positive cores > 50% of Gleason 7 disease; 2-3 intermediate risk factors (Gleason 7; PSA 10-20 ng/mL; or T2b-T2c)
* Patients must have tissue available for Decipher score testing. Results must be available before randomization.
* Serum testosterone ≥ 150 ng/dL determined within 2 months prior to enrollment
* At least 4 weeks must have elapsed from major surgery
* Karnofsky Performance Scale (KPS) ≥ 80%
* Prostate size as determined on MRI to be < 90 cc. Prostate size can be determined on CT scan if MRI is not available
* IPSS ≤ 20
* Patient must be available for follow-up. After 2 years of follow-up, upon completion of post-treatment biopsy, telephone and chart review-based follow-up will be acceptable
* Adequate hepatic function with serum bilirubin less than or equal to 1.5 times the upper institutional limits of normal (ULN), Alanine Aminotransferase (ALT) and Aspartate Aminotransferase (AST) less than or equal to 2.5 x ULN. Patients with a history of Gilbert's syndrome may be enrolled if the total bilirubin is < 3 mg/dL with a predominance of indirect bilirubin
* Adequate renal function with serum creatinine less than or equal to 1.5 x ULN
* Adequate hematologic function with absolute neutrophil counts of at least 1,500 cell/mm3 and platelets of at least 100,000 cells/mm3 and hemoglobin value > 9 g/dL (Note: patients whose anemia has been corrected to a hemoglobin value > 9 g/dL with blood transfusions are allowed).

Exclusion Criteria:

* CT or MRI or Positron Emission Tomography (PET) scan evidence of metastatic disease to the bone
* Patients with one or more positive lymph nodes considered suspicious as determined by clinical assessment on MRI or CT or PET scan
* Prior treatment for prostate cancer, including history of chemotherapy, hormonal therapy within 30 days of enrollment or surgery for prostate cancer (except for prior (transurethral resection of prostate) TURP or greenlight (photoselective vaporization of prostate) PVP which would be allowed)
* History of another malignancy within the previous 2 years except for the following: adequately treated basal cell or squamous cell skin cancer, superficial bladder cancer, currently in complete remission, or any other cancer that has been in complete remission for at least 3 years
* Patients with Crohn's disease or ulcerative colitis

Study Plan

ADT with SBRT

EXPERIMENTAL

The ADT patients will be treated with monthly Degarelix, or Leuprolide injections or daily Relugolix pills. After three months have elapsed, these patients as per routine will undergo SBRT. SBRT comprises stereotactic, ultra-fractionated radiotherapy every other day for five total treatments.

  • DRUG:

    Leuprolide, Degarelix or Relugolix

    Description:

    Patients assigned to the androgen deprivation therapy (ADT) arm will be treated with monthly Degarelix, or Leuprolide injections or daily Relugolix pills which are all standard ADT interventions.
  • RADIATION:

    Stereotactic body radiation therapy/radiosurgery (SBRT)

    Description:

    SBRT will be directed to the prostate and delivered with a prescription dose of 40 Gy in 5 fractions prescribed to the 95% isodose line encompassing the planning target volume. Inter-fraction motion targeting and target position corrections will be utilized for each of the 5 treatment fractions.

SBRT Alone

ACTIVE_COMPARATOR

Participants treated with SBRT alone (standard of care) will be administered stereotactic, ultra-fractionated radiotherapy every other day for five total treatments.

  • RADIATION:

    Stereotactic body radiation therapy/radiosurgery (SBRT)

    Description:

    SBRT will be directed to the prostate and delivered with a prescription dose of 40 Gy in 5 fractions prescribed to the 95% isodose line encompassing the planning target volume. Inter-fraction motion targeting and target position corrections will be utilized for each of the 5 treatment fractions.

Outcome Measures

Primary Outcome Measures

Disease-Free Survival

Time Frame: Up to Year 5

Secondary Outcome Measures

Incidence of Biochemical Failure

Time Frame: Up to Year 5

Incidence of Distant Metastases

Time Frame: Up to Year 5

Overall Survival

Time Frame: Up to Year 5

Number of Positive Post-Treatment Biopsies

Time Frame: Year 2 Post-Treatment (Month 24-30)

Change in Expanded Prostate Cancer Index Composite (EPIC) Questionnaire Score

Time Frame: Baseline, Year 2

Change in International Prostatism Symptom Score (IPSS)

Time Frame: Baseline, Year 2

Change in 12-Item Short Form Health Survey (SF-12) Score

Time Frame: Baseline, Year 2

Timeline

  • Last Updated
    May 3, 2024
  • Start Date
    May 3, 2024
  • Today
    July 1, 2025
  • Completion Date ( Estimated )
    April 16, 2028

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