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Replacing Invasive Cystoscopy With Urine Testing for Non-muscle Invasive Bladder Cancer Surveillance (ReplaceCysto)

Primary Purpose

Non-muscle-invasive Bladder Cancer

Status
Not yet recruiting
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Cystoscopy
Bladder EpiCheck urine test
Xpert Bladder Cancer Monitor urine test
Sponsored by
White River Junction Veterans Affairs Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for Non-muscle-invasive Bladder Cancer focused on measuring Bladder, Cancer, Urology, Cystoscopy, Xpert, EpiCheck, Urine test

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Aged 18 years or older History of low grade intermediate-risk non-muscle invasive bladder cancer, defined as most recent pathology report showing any of the following: multifocal low grade non-invasive urothelial carcinoma of any size solitary low grade non-invasive urothelial carcinoma greater than 3cm in size recurrent low grade non-invasive urothelial carcinoma, with recurrence within 1 year of previous tumor resection Stated willingness to comply with all study procedures and availability for the duration of the study No evidence for recurrence at cystoscopy ≤4 months after most recent tumor resection Ability to consent in English or Spanish Exclusion Criteria: History of total cystectomy of the bladder. History of urinary diversion (e.g., neo-bladder, colon pouch, or ileal conduit). History of muscle-invasive bladder tumor. Pregnancy or lactation. History of urothelial carcinoma of the ureter or renal pelvis status post endoscopic treatment or with evidence of recurrent upper tract disease (inclusion allowed if status post nephroureterectomy and recurrence free at time of inclusion) Anatomic constraints making cystoscopy impossible (e.g., history of urethrectomy, obliterated urethra secondary to stricture). Inability to provide a voided urine sample.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm 3

    Arm Type

    Active Comparator

    Experimental

    Experimental

    Arm Label

    Frequent Cystoscopy

    Xpert Urine Test

    EpiCheck Urine Text

    Arm Description

    Cystoscopy is conducted at 6, 12, 18, and 24 months for patients undergoing surveillance for low grade intermediate-risk non-muscle invasive bladder cancer

    Xpert arm includes urine testing using the Xpert Bladder Cancer Monitor urine test at 6 and 18 months. Cystoscopy is conducted at 12 and 24 months for patients undergoing surveillance for low grade intermediate-risk non-muscle invasive bladder cancer

    EpiCheck arm includes urine testing using the Bladder EpiCheck urine test at 6 and 18 months. Cystoscopy is conducted at 12 and 24 months for patients undergoing surveillance for low grade intermediate-risk non-muscle invasive bladder cancer.

    Outcomes

    Primary Outcome Measures

    Quality of Life Questionnaire-Non-Muscle Invasive Bladder Cancer 24 (EORTC QLQ-NMIBC24)
    Measuring change from baseline. Score range: 0-100. Lower score indicates higher quality of life.

    Secondary Outcome Measures

    Full Information

    First Posted
    March 21, 2023
    Last Updated
    April 4, 2023
    Sponsor
    White River Junction Veterans Affairs Medical Center
    Collaborators
    National Cancer Institute (NCI), University of Texas Southwestern Medical Center, Medical University of South Carolina
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    1. Study Identification

    Unique Protocol Identification Number
    NCT05796375
    Brief Title
    Replacing Invasive Cystoscopy With Urine Testing for Non-muscle Invasive Bladder Cancer Surveillance
    Acronym
    ReplaceCysto
    Official Title
    Replacing Invasive Cystoscopy With Urine Testing for Non-muscle Invasive Bladder Cancer Surveillance
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    April 2023
    Overall Recruitment Status
    Not yet recruiting
    Study Start Date
    August 1, 2023 (Anticipated)
    Primary Completion Date
    April 30, 2028 (Anticipated)
    Study Completion Date
    July 30, 2028 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    White River Junction Veterans Affairs Medical Center
    Collaborators
    National Cancer Institute (NCI), University of Texas Southwestern Medical Center, Medical University of South Carolina

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    Yes
    Device Product Not Approved or Cleared by U.S. FDA
    Yes
    Product Manufactured in and Exported from the U.S.
    No
    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    The purpose of this research is to determine whether bladder cancer monitoring can be improved by replacing some cystoscopy procedures with urine testing. Specifically, this study examines whether there are any differences in urinary symptoms, discomfort, number of invasive procedures, anxiety, complications, cancer recurrence or cancer progression when some cystoscopy procedures are replaced with urine testing.
    Detailed Description
    This is a multi-site randomized phase 2 trial including 240 patients with early-stage bladder cancer, in which patients will be randomized 1:1:1 to programmatic surveillance with the Xpert bladder cancer urine test, the Bladder EpiCheck urine test, or frequent cystoscopy. The primary outcome will be urinary quality of life measured 1 to 3 days after surveillance. This study will have three groups, also called "arms": (1) Frequent Cystoscopy Arm, (2) Xpert Urine Test Arm, and (3) Epicheck Urine Test Arm. The aim of Frequent Cystoscopy is to detect any cancer that might have come back within the bladder by frequently inspecting the bladder. Those in the cystoscopy arm will have a cystoscopy procedure at specified time points for two years. The goal of the Xpert Urine Test arm is to detect any cancer that might have come back within the bladder, while decreasing the number of invasive cystoscopy procedures. Those in the Xpert arm will have a Xpert urine test and a check-up with a medical doctor at 6 months and 18 months, and have a cystoscopy procedure at 12 months and 24 months. The aim of the EpiCheck Urine Test arm is to detect any cancer that might have come back within the bladder, while decreasing the number of invasive cystoscopy procedures. Those in the EpiCheck Urine Test arm will have an Epicheck urine test and a check-up with a medical doctor at 6 months and 18 months and will have a cystoscopy procedure at 12 months and 24 months. The study performance period is 24 months.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Non-muscle-invasive Bladder Cancer
    Keywords
    Bladder, Cancer, Urology, Cystoscopy, Xpert, EpiCheck, Urine test

    7. Study Design

    Primary Purpose
    Health Services Research
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Model Description
    Health care delivery parallel trial with 1:1:1 randomization
    Masking
    None (Open Label)
    Allocation
    Randomized
    Enrollment
    240 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Frequent Cystoscopy
    Arm Type
    Active Comparator
    Arm Description
    Cystoscopy is conducted at 6, 12, 18, and 24 months for patients undergoing surveillance for low grade intermediate-risk non-muscle invasive bladder cancer
    Arm Title
    Xpert Urine Test
    Arm Type
    Experimental
    Arm Description
    Xpert arm includes urine testing using the Xpert Bladder Cancer Monitor urine test at 6 and 18 months. Cystoscopy is conducted at 12 and 24 months for patients undergoing surveillance for low grade intermediate-risk non-muscle invasive bladder cancer
    Arm Title
    EpiCheck Urine Text
    Arm Type
    Experimental
    Arm Description
    EpiCheck arm includes urine testing using the Bladder EpiCheck urine test at 6 and 18 months. Cystoscopy is conducted at 12 and 24 months for patients undergoing surveillance for low grade intermediate-risk non-muscle invasive bladder cancer.
    Intervention Type
    Procedure
    Intervention Name(s)
    Cystoscopy
    Intervention Description
    Cystoscopy entails direct inspection of the bladder via a cystoscope that is inserted into a patient's urethra.
    Intervention Type
    Diagnostic Test
    Intervention Name(s)
    Bladder EpiCheck urine test
    Intervention Description
    The Bladder EpiCheck is a laboratory-developed test for early-stage non-muscle invasive bladder cancer. The Bladder EpiCheck test is a DNA methylation test that is run on DNA extracted from cell pellet from centrifuged urine according to Standardized Operating Procedures. The test has internal controls and a dedicated software to ensure required quality assurance processes and prompt reporting of results.
    Intervention Type
    Diagnostic Test
    Intervention Name(s)
    Xpert Bladder Cancer Monitor urine test
    Intervention Description
    A 4.5 ml sample of voided urine is added to Xpert® Urine Transport Reagent, mixed, and then 4ml of treated urine are transferred to the Sample Chamber of the cartridge. In the cartridge, cells in the urine sample are captured on a filter and lysed by sonication. The released nucleic acid is eluted, mixed with dry RT-PCR reagents, and the solution is transferred to the reaction tube for RT-PCR and detection.
    Primary Outcome Measure Information:
    Title
    Quality of Life Questionnaire-Non-Muscle Invasive Bladder Cancer 24 (EORTC QLQ-NMIBC24)
    Description
    Measuring change from baseline. Score range: 0-100. Lower score indicates higher quality of life.
    Time Frame
    Assessed at 3, 6, 12, 18, and 24 months.

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Aged 18 years or older History of low grade intermediate-risk non-muscle invasive bladder cancer, defined as most recent pathology report showing any of the following: multifocal low grade non-invasive urothelial carcinoma of any size solitary low grade non-invasive urothelial carcinoma greater than 3cm in size recurrent low grade non-invasive urothelial carcinoma, with recurrence within 1 year of previous tumor resection Stated willingness to comply with all study procedures and availability for the duration of the study No evidence for recurrence at cystoscopy ≤4 months after most recent tumor resection Ability to consent in English or Spanish Exclusion Criteria: History of total cystectomy of the bladder. History of urinary diversion (e.g., neo-bladder, colon pouch, or ileal conduit). History of muscle-invasive bladder tumor. Pregnancy or lactation. History of urothelial carcinoma of the ureter or renal pelvis status post endoscopic treatment or with evidence of recurrent upper tract disease (inclusion allowed if status post nephroureterectomy and recurrence free at time of inclusion) Anatomic constraints making cystoscopy impossible (e.g., history of urethrectomy, obliterated urethra secondary to stricture). Inability to provide a voided urine sample.
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Florian R Schroeck, MD, MS
    Phone
    802-295-9363
    Ext
    5368
    Email
    florian.schroeck@va.gov
    First Name & Middle Initial & Last Name or Official Title & Degree
    Laura Jensen, MPH
    Phone
    802-280-5298
    Email
    Laura.Jensen@va.gov
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Florian R Schroeck, MD, MS
    Organizational Affiliation
    White River Junction VA Healthcare System
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Plan to Share IPD
    No
    Citations:
    PubMed Identifier
    29405907
    Citation
    Sayyid RK, Sayyid AK, Klaassen Z, Hersey K, Goldberg H, Perlis N, Ahmad A, Leao R, Chandrasekar T, Fadaak K, Madi R, Terris MK, Finelli A, Hamilton RJ, Kulkarni GS, Zlotta AR, Fleshner NE. Replacing surveillance cystoscopy with urinary biomarkers in followup of patients with non-muscle-invasive bladder cancer: Patients' and urologic oncologists' perspectives. Can Urol Assoc J. 2018 May;12(5):E210-E218. doi: 10.5489/cuaj.4922. Epub 2018 Feb 6.
    Results Reference
    background
    PubMed Identifier
    28739405
    Citation
    Koo K, Zubkoff L, Sirovich BE, Goodney PP, Robertson DJ, Seigne JD, Schroeck FR. The Burden of Cystoscopic Bladder Cancer Surveillance: Anxiety, Discomfort, and Patient Preferences for Decision Making. Urology. 2017 Oct;108:122-128. doi: 10.1016/j.urology.2017.07.016. Epub 2017 Jul 21.
    Results Reference
    background
    PubMed Identifier
    34753702
    Citation
    Laukhtina E, Shim SR, Mori K, D'Andrea D, Soria F, Rajwa P, Mostafaei H, Comperat E, Cimadamore A, Moschini M, Teoh JY, Enikeev D, Xylinas E, Lotan Y, Palou J, Gontero P, Babjuk M, Witjes JA, Kamat AM, Roupret M, Shariat SF, Pradere B; European Association of Urology-Young Academic Urologists (EAU-YAU): Urothelial Carcinoma Working Group. Diagnostic Accuracy of Novel Urinary Biomarker Tests in Non-muscle-invasive Bladder Cancer: A Systematic Review and Network Meta-analysis. Eur Urol Oncol. 2021 Dec;4(6):927-942. doi: 10.1016/j.euo.2021.10.003. Epub 2021 Nov 6. Erratum In: Eur Urol Oncol. 2022 Jan 19;:
    Results Reference
    background
    PubMed Identifier
    31120559
    Citation
    Schroeck FR, Lynch KE, Li Z, MacKenzie TA, Han DS, Seigne JD, Robertson DJ, Sirovich B, Goodney PP. The impact of frequent cystoscopy on surgical care and cancer outcomes among patients with low-risk, non-muscle-invasive bladder cancer. Cancer. 2019 Sep 15;125(18):3147-3154. doi: 10.1002/cncr.32185. Epub 2019 May 23.
    Results Reference
    background

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