Bladder Cancer Clinical Trial
Official title:
A Pilot Study Using Magnetic Resonance Imaging (MRI) to Assess Bladder Motion During Radiotherapy Treatment.
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.
| Status | Not yet recruiting |
| Enrollment | 20 |
| Est. completion date | September 2019 |
| Est. primary completion date | September 2019 |
| Accepts healthy volunteers | No |
| Gender | All |
| Age group | 18 Years and older |
| Eligibility |
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 |
| Country | Name | City | State |
|---|---|---|---|
| n/a | |||
| Lead Sponsor | Collaborator |
|---|---|
| The Christie NHS Foundation Trust |
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Coverage of the Clinical Target Volume for different adaptive radiotherapy strategies | Coverage of the Clinical Target Volume for different adaptive radiotherapy strategies | 18 months | |
| Primary | Dose to the Organs At Risk for different adaptive radiotherapy strategies | Dose to the Organs At Risk for different adaptive radiotherapy strategies | 18 months | |
| Secondary | 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. | 18 months | |
| Secondary | 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 | 18 months |
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