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Brief Title: CISTO: Comparison of Intravesical Therapy and Surgery as Treatment Options for Bladder Cancer
Official Title: CISTO: Comparison of Intravesical Therapy and Surgery as Treatment Options for Bladder Cancer
Study ID: NCT03933826
Brief Summary: Bladder cancer is the most common urinary tract cancer and the 5th most common cancer in the US (1). Yet bladder cancer research is underfunded relative to other common cancers. As a result, bladder cancer care is prone to evidence gaps that produce decision uncertainty for both patients and clinicians. The Comparison of Intravesical Therapy and Surgery as Treatment Options (CISTO) for Bladder Cancer Study has the potential to fill these critical evidence gaps, change care pathways for the management of NMIBC (non-muscle-invasive bladder cancer), and provide for personalized, patient-centered care. The purpose of CISTO is to conduct a large prospective study that directly compares the impact of medical management versus bladder removal in recurrent high-grade NMIBC patients with BCG (Bacillus Calmette-Guerin) failure on clinical outcomes and patient and caregiver experience using standardized patient-reported outcomes (PROs).
Detailed Description: Most bladder cancer patients (74%) present with NMIBC where the cancer is limited to the lining or support layer of the bladder. High-grade NMIBC is treated initially with endoscopic resection and intravesical immunotherapy, followed by bladder instillations of BCG. Most patients with high-risk, high-grade NMIBC are able to retain their bladders and avoid more invasive treatments. However, 24-61% of patients will have their cancers recur within 12 months of treatment with BCG (BCG failures), and they have limited treatment options. National guidelines recommend consideration between two alternatives: additional medical management and radical cystectomy (removal of the bladder). Selecting between these options involves weighing the risk of progression of bladder cancer and loss of a window of potential cure versus the risk of morbidity and loss of quality of life (QOL) with bladder removal. This complex decision-making engages patients and their caregivers, who may be impacted by the urinary, sexual, and bowel dysfunctions that can occur with NMIBC treatment. The investigators will evaluate this research question on a large scale in real world practice settings including academic and community-based practices and examine patient-centered outcomes. The investigators have engaged stakeholders with diverse perspectives relevant to this research question, including patients, caregivers, national patient advocacy organizations, national medical specialty organizations, guideline developers, health care payers, and industry. By engaging broad expertise relevant to this research question, the investigators will ensure that the study results will help NMIBC patients whose cancer recurs after BCG treatment make more informed decisions that improve the health outcomes that are important to them. CISTO is an observational study that will not affect the treatment that patients chose. Patient surveys will occur at study entry and at follow-up assessments for up to four years. There will also be a qualitative sub-study that will include interviews of approximately 50 patients and 25 caregivers recruited from the observational cohort study.
Minimum Age: 18 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
University of Alabama at Birmingham, Birmingham, Alabama, United States
Mayo Clinic Cancer Center, Phoenix, Arizona, United States
USC/Norris Comprehensive CA Center, Los Angeles, California, United States
UCLA, Los Angeles, California, United States
Hoag Memorial Hospital Presbyterian, Newport Beach, California, United States
University of Colorado Anschutz Medical Campus, Aurora, Colorado, United States
University of Miami, Miami, Florida, United States
H. Lee Moffitt Cancer Center & Research Institute, Tampa, Florida, United States
Emory University, Atlanta, Georgia, United States
University of Chicago, Chicago, Illinois, United States
University of Iowa, Iowa City, Iowa, United States
University of Kansas Medical Center, Kansas City, Kansas, United States
LSU Healthcare Network - Multi Specialty Clinic, Metairie, Louisiana, United States
Johns Hopkins University, School of Medicine, Baltimore, Maryland, United States
Chesapeake Urology Research Associates, Hanover, Maryland, United States
Brigham and Women's Hospital, Boston, Massachusetts, United States
Michigan Medicine Rogel Cancer Center, Ann Arbor, Michigan, United States
Spectrum Health, Grand Rapids, Michigan, United States
Comprehensive Urology -- A Division of Michigan Healthcare Professionals, Royal Oak, Michigan, United States
Albert Einstein College of Medicine, Bronx, New York, United States
University of North Carolina, Chapel Hill, North Carolina, United States
Levine Cancer Institute, Charlotte, North Carolina, United States
The Ohio State University, Columbus, Ohio, United States
Stephenson Cancer Center, Oklahoma City, Oklahoma, United States
Asante Rogue Regional Medical Center, Medford, Oregon, United States
Geisinger Medical Center, Danville, Pennsylvania, United States
Fox Chase Cancer Center, Philadelphia, Pennsylvania, United States
Perelman Center for Advanced Medicine, Philadelphia, Pennsylvania, United States
Carolina Urologic Research Center, LLC, Myrtle Beach, South Carolina, United States
Urology Associates, P.C., Nashville, Tennessee, United States
Vanderbilt University Medical Center, Nashville, Tennessee, United States
UT Southwestern Medical Center, Dallas, Texas, United States
MD Anderson Cancer Center, Houston, Texas, United States
The University of Texas Health Science Center at San Antonio, San Antonio, Texas, United States
University of Utah, Salt Lake City, Utah, United States
University of Washington, Seattle, Washington, United States
Name: John L Gore, MD
Affiliation: University of Washington
Role: PRINCIPAL_INVESTIGATOR