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MRI in Clinical Staging and Estimation of Treatment Response in Bladder Cancer (MIB)

Primary Purpose

Bladder Cancer

Status
Completed
Phase
Not Applicable
Locations
Finland
Study Type
Interventional
Intervention
MR imaging
Sponsored by
Turku University Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Bladder Cancer focused on measuring bladder cancer, MRI, TUR-BT, cystectomy, chemotherapy

Eligibility Criteria

18 Years - 85 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age: 18 to 85 years old
  • Suspected BC based on cystoscopical evaluation.
  • Mental status: Patients must be able to understand the meaning of the study
  • Informed consent: The patient must sign the appropriate Ethical Committee (EC) approved informed consent documents in the presence of the designated staff

Exclusion Criteria:

  • History of serious cardiovascular, liver or kidney disease
  • Uncontrolled serious infection
  • Contraindications for MRI (cardiac pacemaker, intracranial clips etc)
  • Patient refusing radical cystectomy or chemotherapy or BCG
  • Intravesical Bacillus Calmette-Guerin instillations within 6 months before the first MRI examination

Sites / Locations

  • Department of Urology, Central Hospital of Pori
  • University of Turku

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

MRI and biomarkers in bladder cancer

Arm Description

Utilization of MR-imaging and biomarkers to stage bladder cancer and in estimation of chemosensitivity

Outcomes

Primary Outcome Measures

Accuracy of the multiparametric MRI (anatomical MRI, DCE-MRI, DWI) in the staging of bladder cancer
The accuracy of multiparametric MRI (anatomical MRI, DCE-MRI, DWI) in the staging of bladder cancer will be evaluated using transurethral resection of bladder tumor and cystectomy specimens

Secondary Outcome Measures

Prediction of response to neo-adjuvant chemotherapy and/or BCG treatment evaluated by multiparametric MRI (anatomical MRI, DCE-MRI, DWI)
The aim is to evaluate predictive power of multiparametric MRI for estimation neo-adjuvant chemotherapy and/or BCG treatment response. Multiparametric MRI will be performed before neo-adjuvant chemotherapy and/or BCG treatment and patients will be followed using standard clinical follow up and/or undergo cystectomy.

Full Information

First Posted
January 5, 2015
Last Updated
June 16, 2020
Sponsor
Turku University Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT02662166
Brief Title
MRI in Clinical Staging and Estimation of Treatment Response in Bladder Cancer
Acronym
MIB
Official Title
Magnetic Resonance Imaging of Bladder Cancer
Study Type
Interventional

2. Study Status

Record Verification Date
June 2020
Overall Recruitment Status
Completed
Study Start Date
July 2014 (Actual)
Primary Completion Date
July 10, 2019 (Actual)
Study Completion Date
May 1, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Turku University Hospital

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Bladder cancer (BC) as the most common malignancy arising from the urinary tract continues to be a major health problem. This prospective non-randomized study will enroll 150 patients undergoing magnetic resonance imaging (MRI) at different stages of their diagnostic and therapeutical process. The enrolled patients with suspected BC (BC) based on cystoscopy will have their initial MRI examination before transurethral resection of bladder tumor (TUR-BT) and biomarker collection. After pathology review of the histological specimens, patients will be treated according to standard clinical practice. The second MRI examination will be performed before therapeutic intervention, if TUR-BT alone is not sufficient enough. Neoadjuvant chemotherapy will be applied in high risk patients having muscle invasison, while intermediate risk patient - T1 high grade or carcinoma in situ patients - will be treated using Bacillus Calmette-Guerin (BCG) instilliations. After the completion of the neoadjuvant chemotherapy or BCG treatment, the patients will undergo the third MRI examination. Low risk patients will be followed by annual with MRI examination.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Bladder Cancer
Keywords
bladder cancer, MRI, TUR-BT, cystectomy, chemotherapy

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
50 (Actual)

8. Arms, Groups, and Interventions

Arm Title
MRI and biomarkers in bladder cancer
Arm Type
Experimental
Arm Description
Utilization of MR-imaging and biomarkers to stage bladder cancer and in estimation of chemosensitivity
Intervention Type
Device
Intervention Name(s)
MR imaging
Intervention Description
3 T MRI of the urinary bladder
Primary Outcome Measure Information:
Title
Accuracy of the multiparametric MRI (anatomical MRI, DCE-MRI, DWI) in the staging of bladder cancer
Description
The accuracy of multiparametric MRI (anatomical MRI, DCE-MRI, DWI) in the staging of bladder cancer will be evaluated using transurethral resection of bladder tumor and cystectomy specimens
Time Frame
24 months
Secondary Outcome Measure Information:
Title
Prediction of response to neo-adjuvant chemotherapy and/or BCG treatment evaluated by multiparametric MRI (anatomical MRI, DCE-MRI, DWI)
Description
The aim is to evaluate predictive power of multiparametric MRI for estimation neo-adjuvant chemotherapy and/or BCG treatment response. Multiparametric MRI will be performed before neo-adjuvant chemotherapy and/or BCG treatment and patients will be followed using standard clinical follow up and/or undergo cystectomy.
Time Frame
24 months
Other Pre-specified Outcome Measures:
Title
Estimation of chemosensitivity
Description
Prevalence of patients responding neo-adjuvant chemotherapy, compared with the non-responders as evaluated by cystectomy specimens, according to various biomarkers and ex vivo tissue culturing will be evaluated.
Time Frame
24 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age: 18 to 85 years old Suspected BC based on cystoscopical evaluation. Mental status: Patients must be able to understand the meaning of the study Informed consent: The patient must sign the appropriate Ethical Committee (EC) approved informed consent documents in the presence of the designated staff Exclusion Criteria: History of serious cardiovascular, liver or kidney disease Uncontrolled serious infection Contraindications for MRI (cardiac pacemaker, intracranial clips etc) Patient refusing radical cystectomy or chemotherapy or BCG Intravesical Bacillus Calmette-Guerin instillations within 6 months before the first MRI examination
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Peter Boström, MD, PhD
Organizational Affiliation
Department of Urology, University of Turku and Turku University Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Department of Urology, Central Hospital of Pori
City
Pori
Country
Finland
Facility Name
University of Turku
City
Turku
ZIP/Postal Code
20100
Country
Finland

12. IPD Sharing Statement

Citations:
PubMed Identifier
34448679
Citation
Nikulainen I, Salminen AP, Jambor I, Merisaari H, Tammilehto V, Taimen P, Seikkula H, Bostrom PJ. Visual MRI T-category versus VI-RADS evaluation from multiparametric MRI in the detection of muscle-invasion in patients with suspected bladder cancer: single centre registered clinical trial (MIB-trial). Scand J Urol. 2021 Oct;55(5):354-360. doi: 10.1080/21681805.2021.1971290. Epub 2021 Aug 27.
Results Reference
derived

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MRI in Clinical Staging and Estimation of Treatment Response in Bladder Cancer

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