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A Study Using MRI To Assess Bladder Motion During Radiotherapy

Primary Purpose

Bladder Cancer

Status
Unknown status
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
MRI Scan
Sponsored by
The Christie NHS Foundation Trust
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for Bladder Cancer focused on measuring bladder, radiotherapy, magnetic resonance imaging

Eligibility Criteria

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

Inclusion Criteria:

  • Histologically confirmed diagnosis of bladder cancer
  • Treatment with primary curative intent
  • Undergoing external beam radiotherapy (+/-chemotherapy)
  • Age over 18 years

Exclusion Criteria:

  • Any contraindications to MRI identified after MRI safety screening including completion of an MRI Safety Screening Form
  • Any contraindications to both Hyoscine Butylbromide (Buscopan)
  • Previous cystectomy
  • Unable to tolerate MRI scans
  • Metastatic disease
  • Pregnancy

Sites / Locations

    Arms of the Study

    Arm 1

    Arm Type

    Experimental

    Arm Label

    MRI Scan

    Arm Description

    As part of the study patients will undergo 4 MRI scans during radiotherapy treatment. These will take place during the 1st, 2nd, 3rd and 4th week of treatment

    Outcomes

    Primary Outcome Measures

    Coverage of the Clinical Target Volume for different adaptive radiotherapy strategies
    Coverage of the Clinical Target Volume for different adaptive radiotherapy strategies
    Dose to the Organs At Risk for different adaptive radiotherapy strategies
    Dose to the Organs At Risk for different adaptive radiotherapy strategies

    Secondary Outcome Measures

    Diffusion Weighted Imaging on MR prior to and during treatment and clinical response to treatment on post treatment cystoscopy.
    Diffusion Weighted Imaging on MR prior to and during treatment and clinical response to treatment on post treatment cystoscopy.
    Bladder filling using MR sequences and stratification of patients into large or small bladder and tumour bed motion
    Bladder filling using MR sequences and stratification of patients into large or small bladder and tumour bed motion

    Full Information

    First Posted
    January 10, 2018
    Last Updated
    January 29, 2018
    Sponsor
    The Christie NHS Foundation Trust
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    1. Study Identification

    Unique Protocol Identification Number
    NCT03409029
    Brief Title
    A Study Using MRI To Assess Bladder Motion During Radiotherapy
    Official Title
    A Pilot Study Using Magnetic Resonance Imaging (MRI) to Assess Bladder Motion During Radiotherapy Treatment.
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    January 2018
    Overall Recruitment Status
    Unknown status
    Study Start Date
    March 2018 (Anticipated)
    Primary Completion Date
    September 2019 (Anticipated)
    Study Completion Date
    September 2019 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    The Christie NHS Foundation Trust

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    The standard non-surgical treatment for muscle invasive bladder cancer is concurrent chemo-radiotherapy. This treatment is associated with long term side effects in around a third of patients with up to 12% suffering from grade 3-4 toxicity. Effective radiotherapy depends on delivering a curative dose to the target whilst minimising dose to surrounding tissues to reduce toxicities. As an organ that constantly varies in shape and position, achieving this in bladder irradiation is challenging. Cone beam Computed Tomography (CBCT) has allowed visualisation of soft tissue on treatment and hence image-guided treatment and improved accuracy, but the image quality of CBCT is suboptimal for distinguishing soft tissue boundaries. On the other hand, MRI scans produce superior soft tissue definition and visualisation of tumour bed. This would in turn allow for various ways of optimising treatment and potentially improving outcome. There have been a number of studies evaluating pelvic organ motion in bladder cancer as well as assessing different adaptive radiotherapy strategies. These have included individualized margins, plan of the day and adaptive techniques. Most of these studies have been carried out using CBCT imaging which is often poor quality with limited soft tissue contrast. MRI offers better visualization of the tumour bed and organs at risk (OARs). As a result, the utilisation of MRI in radiotherapy could allow for increased radiation dose to the tumour bed while maintaining minimal dose to surrounding soft tissue. This study will explore the role of MRI imaging in adaptive radiotherapy for bladder cancer with development of a number of theoretical treatment strategies.
    Detailed Description
    Patients will undergo standard treatment during the study with four weeks of external beam radiotherapy (20 fractions). They will be treated with weekly Gemcitabine (100mg/m2) or daily Nicotinamide (60mg/kg)/Carbogen (2% carbon dioxide, 98% oxygen at 15 litres per minute) if clinically appropriate. As part of standard treatment patients will have a staging CT scan at diagnosis and a radiotherapy planning CT. Cone beam imaging will also be performed. Response will be assessed as standard with cystoscopy at 3 months and CT scan at 12 months. As part of the study patients will undergo 4 additional MRI scans. These will take place in the 1st, 2nd, 3rd and 4th weeks of treatment. These MRI scans will include anatomical images - with full and empty bladder as well as cine data (with a scan every minute for 10 minutes) to assess intra fraction motion. They will also include a diffusion weighted imaging (DWI) sequence, which will be used to assess if early prediction of response is possible. The frequency of cone beam imaging will be increased from 6 scans (minimum) as standard of care to 20 scans to allow for daily imaging. The 1st MRI scan will be contoured to outline the tumour bed, clinical target volumes (CTVs) and OARs. A variety of planning strategies will be developed including standard planning target volume (PTV) margins, a plan of the day (POTD) approach, a POTD+ as well as an online adaptation model. These models will be used to assess coverage of CTV and PTV, and the feasibility of increasing radiation dose to the tumour bed, as well as dose to OARs using the scans obtained during the radiotherapy treatment. The practicality of each approach will also be assessed. Inter and intra fraction organ and tumour bed motion will also be analysed in order to develop patient specific models.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Bladder Cancer
    Keywords
    bladder, radiotherapy, magnetic resonance imaging

    7. Study Design

    Primary Purpose
    Basic Science
    Study Phase
    Not Applicable
    Interventional Study Model
    Single Group Assignment
    Model Description
    Single site, non-randomised basic science study
    Masking
    None (Open Label)
    Allocation
    N/A
    Enrollment
    20 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    MRI Scan
    Arm Type
    Experimental
    Arm Description
    As part of the study patients will undergo 4 MRI scans during radiotherapy treatment. These will take place during the 1st, 2nd, 3rd and 4th week of treatment
    Intervention Type
    Diagnostic Test
    Intervention Name(s)
    MRI Scan
    Intervention Description
    Additional imaging using MRI scan
    Primary Outcome Measure Information:
    Title
    Coverage of the Clinical Target Volume for different adaptive radiotherapy strategies
    Description
    Coverage of the Clinical Target Volume for different adaptive radiotherapy strategies
    Time Frame
    18 months
    Title
    Dose to the Organs At Risk for different adaptive radiotherapy strategies
    Description
    Dose to the Organs At Risk for different adaptive radiotherapy strategies
    Time Frame
    18 months
    Secondary Outcome Measure Information:
    Title
    Diffusion Weighted Imaging on MR prior to and during treatment and clinical response to treatment on post treatment cystoscopy.
    Description
    Diffusion Weighted Imaging on MR prior to and during treatment and clinical response to treatment on post treatment cystoscopy.
    Time Frame
    18 months
    Title
    Bladder filling using MR sequences and stratification of patients into large or small bladder and tumour bed motion
    Description
    Bladder filling using MR sequences and stratification of patients into large or small bladder and tumour bed motion
    Time Frame
    18 months

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Histologically confirmed diagnosis of bladder cancer Treatment with primary curative intent Undergoing external beam radiotherapy (+/-chemotherapy) Age over 18 years Exclusion Criteria: Any contraindications to MRI identified after MRI safety screening including completion of an MRI Safety Screening Form Any contraindications to both Hyoscine Butylbromide (Buscopan) Previous cystectomy Unable to tolerate MRI scans Metastatic disease Pregnancy
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Sally Falk
    Phone
    0044 161 446 8318
    Email
    sally.falk@christie.nhs.uk
    First Name & Middle Initial & Last Name or Official Title & Degree
    Yee Pei Song
    Phone
    0044 161 446 8318
    Email
    yeepei.song@christie.nhs.uk
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Ananya Choudhury, MA, PhD
    Organizational Affiliation
    The Christie NHS Foundation Trust
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Plan to Share IPD
    No

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    A Study Using MRI To Assess Bladder Motion During Radiotherapy

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