Skip to content

Multifunctional Magnetic Resonance (MR) for Radiotherapy Planning in Prostate Cancer

Multifunctional MR for Radiotherapy Planning in Prostate Cancer

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01006564
Enrollment
30
Registered
2009-11-03
Start date
2009-03-31
Completion date
2011-06-30
Last updated
2009-11-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Prostate Cancer

Keywords

Magnetic Resonance Imaging, Prostate Cancer, Magnetic Resonance Spectroscopy, Radiotherapy planning

Brief summary

To determine if functional MRI methods will aid planning of a radiation dose boost within the prostate in patients with prostate cancer potentially improving safety and efficacy.

Interventions

OTHERImaging Investigations (not radiation)

Pre-hormone therapy MRI scans will be performed as an adjunct to the patients' staging MRI scan; post hormone MRI will be done wholly for research purposes.

OTHEROther

Insertion of gold seeds into prostate for image registration.

Sponsors

Institute of Cancer Research, United Kingdom
CollaboratorOTHER
Royal Marsden NHS Foundation Trust
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC

Eligibility

Sex/Gender
MALE
Age
16 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Hormone therapy naive patients planned to be treated by radical radiotherapy after 3-6 months of androgen suppression * Patients with low-high risk histologically confirmed localised disease are eligible, with WHO performance status 0-1.

Exclusion criteria

* Patients unsuitable for functional MRI of the prostate or gold seed fiducial marker insertion (e.g. patients unable to tolerate endorectal MRI examination). * No prior pelvic radiotherapy or radical prostatectomy, previous androgen therapy, patients unsuitable for radical radiotherapy, life expectancy \<10 years, previous active malignancy within last 5 years, co-morbid conditions likely to impact on the advisability of radical radiotherapy, full anticoagulation, other exclusions to MRI (e.g. hip prosthesis or fixation, claustrophobia, ferromagnetic implants).

Design outcomes

Primary

MeasureTime frame
Comparison of dose distributions produced by rival radiotherapy plans judged using radiobiological model predictions of Tumour Control Probability (TCP) and Normal Tissue Complication Probability (NTCP).

Secondary

MeasureTime frame
Comparison of reproducibility of registration algorithms for mapping functional MR data acquired before hormone therapy to MR anatomical data acquired after hormone therapy and prior to radiotherapy.
Comparison of reproducibility of registration of functional and MR data with computed tomography (CT) data using gold seed registration, assessing reproducibility and positioning issues.
Comparison of image quality, registration reproducibility and gland distortion of internal and external imaging coils for MRI image acquisition and registration of the prostate.
Comparison of dose distributions produced by rival radiotherapy plans judged using three standard dose-volume constraints for targets and normal tissues and careful examination of the 3D dose distribution.

Countries

United Kingdom

Contacts

Primary ContactDr Nandita deSouza
nandita.desouza@icr.ac.uk02086613289

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026