Hypo-fractionated Radiation Therapy With or Without Androgen Suppression for Intermediate Risk Prostate Cancer

Phase 3

Recruiting

• Conditions: Prostate Cancer
• Interventions: Radiation: Radiation; Drug: Androgen Suppression Therapy

• Registration Number: NCT01492972
• Lead Sponsor: Proton Collaborative Group

Brief Summary

The purpose of this study is to compare the effects, good and/or bad of two treatment methods on subjects and their cancer.

Proton beam radiation therapy is one of the treatments for men with prostate cancer who have localized disease. The benefit of the combination with androgen suppression is not completely understood. This study will compare the use of hypofraction proton therapy (28 treatments) alone to proton therapy with androgen suppression therapy.

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2011-12-09
• Study First Submitted QC: 2011-12-13
• Study First Posted: 2011-12-15
• Study Start: 2012-01
• Status Verified: 2024-05
• Last Update Submitted: 2024-05-30
• Last Update Posted: 2024-06-03
• Primary Completion: 2025-12

Recruitment & Eligibility

• Status: RECRUITING
• Sex: Male
• Target Recruitment: 192

Inclusion Criteria

• Histologically confirmed prostate adenocarcinoma (within 365 days of randomization) at intermediate risk for reoccurrence determined by at least one of the following: Gleason Score 7, PSA > = 10 and < = 20, T stage T2b - T2c
• Clinical stages T1-T2c N0 M0 as staged by the treating investigator. (AJCC Criteria 7th Ed.- appendix III).
• Histological evaluation of prostate biopsy with assignment of a Gleason score to the biopsy material; Gleason score must be in the range of 2-7. > 6 cores are strongly recommended.
• PSA values < = 20 ng/ml within 90 days prior to randomization. Obtained prior to biopsy or at least 21 days after prostate biopsy.
• ECOG performance status 0-1 (appendix II) assessed within 90 days of randomization.
• Patients must sign IRB approved study specific informed consent.
• Patients must complete all required pre-entry tests listed in section 4.0 within the specified time frames.
• Patients must be able to start treatment within 56 days of randomization.
• Patients must be at least 18 years old.
• For brachytherapy, an IPSS ≤ 21, or ≤ 17 if patient is on medications to improve urination.
• For brachytherapy, prostate volume must be less than 55cc prior to AS.

Exclusion Criteria

• Pelvic lymph nodes > 1.5 cm in greatest dimension unless the enlarged lymph node is biopsied and negative.
• Previous prostate cancer surgery to include: prostatectomy, hyperthermia and cryosurgery.
• Previous pelvic radiation for prostate cancer.
• Previous androgen suppression therapy for prostate cancer.
• Active rectal diverticulitis, Crohn's disease affecting the rectum or ulcerative colitis (non-active diverticulitis and Crohn's disease not affecting the rectum are allowed).
• Prior systemic chemotherapy for prostate cancer.
• History of proximal urethral stricture requiring dilatation.
• Current and continuing anticoagulation with warfarin sodium (Coumadin), heparin, low- molecular weight heparin, Clopidogrel bisulfate (Plavix), or equivalent (unless it can be stopped to manage treatment related toxicity or to have a biopsy if needed).
• Major medical, addictive or psychiatric illness which in the investigator's opinion, will prevent the consent process, completion of the treatment and/or interfere with follow-up. (Consent by legal authorized representative is not permitted for this study).
• Evidence of any other cancer within the past 5 years and < 50% probability of a 5 year survival. (Prior or concurrent diagnosis of basal cell or non-invasive squamous cell cancer of the skin is allowed).
• History of myocardial infarction within the last 6 months.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Radiation + Androgen Suppression	Androgen Suppression Therapy	Androgen Suppression Therapy x 6 months + Radiation
Radiation Alone	Radiation	Proton Radiation Total Dose=70 Gy(RBE) OR High Dose Radiation with IMRT Alone=81 Gy OR Intraoperative LDR Brachytherapy and IMRT=45 Gy
Radiation + Androgen Suppression	Radiation	Androgen Suppression Therapy x 6 months + Radiation

Primary Outcome Measures

Name	Time	Method
Morbidity Outcomes	after the initial 100 patients have had a median follow up of at least three years and then every year.	To determine if androgen suppression along with radiation therapy will result in a higher freedom from failure (FFF) than radiation therapy without androgen suppression.; Freedom from failure (FFF): The events for FFF will be the first occurrence of clinical failure (local recurrence, regional recurrence, or distant metastasis), biochemical failure by the Phoenix definition (PSA ≥ 2 ng/ml over the current nadir PSA) (45) discounting bounces per investigator discretion, or the start of salvage therapy including androgen suppression

Secondary Outcome Measures

Name	Time	Method
Frequency and severity of grade 2 or higher GU and GI toxicity	At 6 months	Assessment of grade 2 or higher GU and GI toxicity using CTCAE 4.0 criteria
Frequency and severity of GI and GU toxicity	At 3 years
Incidence of Freedom from biochemical failure (FFBF)	At 5 years
Incidence of clinical failure: local and/or distant	At 5 years
Correlate pathologic and radiologic findings with outcomes	At 5 years
Prospectively collect information that will help to define dose-volume relationships of normal structures with acute and chronic toxicity	At 3 years
Incidence of quality of life issues	At completion of radiation therapy
Incidence of progression free survival: using clinical, biochemical and SAD as events	At 5 years
Correlate testosterone levels and variation with proton therapy and outcomes	At 5 years
Incidence of salvage Androgen Suppression use (SAD)	At 5 years
Incidence of disease-specific survival	At 5 years
Incidence of overall survival	At 5 years
Correlate PSA and free PSA levels with outcomes	At 5 years

Trial Locations

Locations (4)

Mayo Clinic; 🇺🇸 Scottsdale, Arizona, United States

Oklahoma Proton Center; 🇺🇸 Oklahoma City, Oklahoma, United States

Northwestern Medicine Chicago Proton Center; 🇺🇸 Warrenville, Illinois, United States

Hampton University Proton Therapy Institute; 🇺🇸 Hampton, Virginia, United States