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Spots Global Cancer Trial Database for Radiation Therapy in Treating Patients With Prostate Cancer

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Trial Identification

Brief Title: Radiation Therapy in Treating Patients With Prostate Cancer

Official Title: A Randomized Phase II Trial of Hypofractionated Radiotherapy for Favorable Risk Prostate Cancer

Study ID: NCT01434290

Study Description

Brief Summary: RATIONALE: Radiation therapy uses high-energy x-rays to kill tumor cells. Specialized radiation therapy that delivers a high dose of radiation directly to the tumor may kill more tumor cells and cause less damage to normal tissue. Given radiation therapy in different ways may kill more tumor cells. PURPOSE: This randomized phase II trial studies radiation therapy to see how well it works in treating patients with prostate cancer.

Detailed Description: OBJECTIVES: Primary * To demonstrate that 1-year health-related quality of life (HRQOL) for at least one hypofractionated arm is not significantly lower than baseline as measured by the Bowel and Urinary domains of the Expanded Prostate Cancer Index Composite (EPIC) instrument. Secondary * To estimate the degree of change in HRQOL in each arm for the Sexual and Hormonal EPIC domains and the Utilization of Sexual Medications/Devices from baseline to 1 year, 2 years, and 5 years. * To estimate the degree of change in global HRQOL in each arm as measured by the Euro Quality of Life, 5 dimensions (EQ-5D) from baseline to 1 year, 2 years, and 5 years. * To estimate the rate of acute and late gastrointestinal (GI) and genitourinary (GU) toxicity for each arm at 1, 2, and 5 years. * To estimate prostate-specific antigen (PSA) failure in each arm at 1, 2, and 5 years. * To estimate disease-free survival (DFS) in each arm at 1, 2, and 5 years. * To estimate Quality Adjusted Life Years for each arm at 1, 2, and 5 years using the EQ-5D and DFS. * To identify genetic markers associated with normal tissue toxicities resulting from radiotherapy. * To collect tumor tissue for biomarker studies. * To estimate EPIC bowel and urinary HRQOL as continuous variables. OUTLINE: This is a multicenter study. Patients are stratified according to treatment techniques/machine (all linear accelerator-based treatment \[excluding cyberknife\] vs cyberknife vs protons). Patients are randomized to 1 of 2 treatment arms. * Arm I: Patients undergo hypofractionated radiotherapy using intensity-modulated radiation therapy (IMRT), cyberknife, or protons twice a week for approximately 2½ weeks (36.25 Gy total). * Arm II: Patients undergo hypofractionated radiotherapy using IMRT, cyberknife, or protons once a day, 5 days a week, for approximately 2½ weeks (51.6 Gy total). Patients may undergo blood and tumor tissue collection for correlative studies. Patients may also complete the Utilization of Sexual Medications/Devices, the European Questionnaire-5D, and the Bowel and Urinary domains of the Expanded Prostate Cancer Index Composite (EPIC) questionnaires at baseline and at 1, 2, and 5 years after completion of radiation therapy. After completion of study therapy, patients are followed-up every 3 months for 2 years, every 6 months for 3 years, and then annually thereafter.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: MALE

Healthy Volunteers: No

Locations

UAB Comprehensive Cancer Center, Birmingham, Alabama, United States

Arizona Center for Cancer Care - Peoria, Peoria, Arizona, United States

Arizona Oncology Services Foundation, Phoenix, Arizona, United States

Kaiser Permanente - Division of Research - Oakland, Oakland, California, United States

Rohnert Park Cancer Center, Rohnert Park, California, United States

Kaiser Permanente Medical Center - Roseville, Roseville, California, United States

UCSF Helen Diller Family Comprehensive Cancer Center, San Francisco, California, United States

Kaiser Permanente Santa Clara Medical Center, Santa Clara, California, United States

Kaiser Permanente Medical Center - South San Francisco, South San Francisco, California, United States

Urology Center of Colorado, Denver, Colorado, United States

Emory Crawford Long Hospital, Atlanta, Georgia, United States

Winship Cancer Institute of Emory University, Atlanta, Georgia, United States

Queen's Cancer Institute at Queen's Medical Center, Honolulu, Hawaii, United States

Boston University Cancer Research Center, Boston, Massachusetts, United States

Beth Israel Deaconess Medical Center, Boston, Massachusetts, United States

Mayo Clinic Cancer Center, Rochester, Minnesota, United States

Siteman Cancer Center at Barnes-Jewish Hospital - Saint Louis, Saint Louis, Missouri, United States

Lineberger Comprehensive Cancer Center at University of North Carolina - Chapel Hill, Chapel Hill, North Carolina, United States

Case Comprehensive Cancer Center, Cleveland, Ohio, United States

Oklahoma University Cancer Institute, Oklahoma City, Oklahoma, United States

Natalie Warren Bryant Cancer Center at St. Francis Hospital, Tulsa, Oklahoma, United States

Rosenfeld Cancer Center at Abington Memorial Hospital, Abington, Pennsylvania, United States

Rothman Specialty Hospital, Bensalem, Pennsylvania, United States

Fox Chase Cancer Center Buckingham, Furlong, Pennsylvania, United States

Academic Urology Prostate Center, King Of Prussia, Pennsylvania, United States

Kimmel Cancer Center at Thomas Jefferson University - Philadelphia, Philadelphia, Pennsylvania, United States

Fox Chase Cancer Center - Philadelphia, Philadelphia, Pennsylvania, United States

Hollings Cancer Center at Medical University of South Carolina, Charleston, South Carolina, United States

Gibbs Regional Cancer Center at Spartanburg Regional Medical Center, Spartanburg, South Carolina, United States

University of Virginia Cancer Center, Charlottesville, Virginia, United States

Columbia-Saint Mary's Cancer Care Center, Milwaukee, Wisconsin, United States

Medical College of Wisconsin Cancer Center, Milwaukee, Wisconsin, United States

Cross Cancer Institute at University of Alberta, Edmonton, Alberta, Canada

Margaret and Charles Juravinski Cancer Centre, Hamilton, Ontario, Canada

Grand River Regional Cancer Centre at Grand River Hospital, Kitchener, Ontario, Canada

London Regional Cancer Program at London Health Sciences Centre, London, Ontario, Canada

Hopital Notre-Dame du CHUM, Montreal, Quebec, Canada

Contact Details

Name: Himu R. Lukka, MD

Affiliation: Margaret and Charles Juravinski Cancer Centre

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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