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
About this trial
This is an interventional basic science trial for Bladder Cancer focused on measuring bladder, radiotherapy, magnetic resonance imaging
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
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
NCT ID
NCT03409029
First Posted
January 10, 2018
Last Updated
January 29, 2018
Sponsor
The Christie NHS Foundation Trust
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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