BIOPROP20: Biologically Optimised IMRT for Prostate Radiotherapy Hypofractionated Radiotherapy With Intra-prostatic Boosts to Tumour Nodules in Men With Intermediate and High Risk Prostate Cancer (BIOPROP20)
Primary Purpose
Prostate Cancer
Status
Completed
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
Hypofractionated IMRT boost Radiotherapy
Sponsored by

About this trial
This is an interventional treatment trial for Prostate Cancer
Eligibility Criteria
Inclusion Criteria:
- Histologically confirmed adenocarcinoma of the prostate
- NCCN intermediate/high risk disease and estimated risk of lymph node involvement 15 - 40%*
- MRI stage T2a-T4 N0M0
- Age 18-80 years
- Normal blood count (Hb >11g/dl, WBC > 4000/mm3, platelets >100,000/mm3)
- WHO performance status 0 or 1
Fully informed written consent
- Risk of pelvic lymph node involvement = (Gleason score - 6) x 10 + 2/3 PSA
Exclusion Criteria:
- Prior radiotherapy to the prostate or pelvis
- Prior hormone therapy or radical prostatectomy
- Total hip replacement
- Clinically significant inflammatory bowel disease
- Contraindication to have diagnostic MRI scans
- Unable to have a general anaesthetic
- Anti-coagulant therapy which cannot be temporarily stopped
Sites / Locations
- The Clatterbridge Cancer Centre NHS Foundation Trust
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Hypofractionated IMRT boost Radiotherapy
Arm Description
Outcomes
Primary Outcome Measures
Acute bladder and bowel toxicity (NCI CTCAE v 4.0 and RTOG) at 18 weeks after the commencement of radiotherapy treatment
Secondary Outcome Measures
The success rate of producing dose painted IMRT plans which fulfill the dose-volume constraints as specified for the prostate and for the normal tissues
Late bladder and bowel toxicity (NCI CTCAE v4) at 2 years
Full Information
NCT ID
NCT02125175
First Posted
April 17, 2014
Last Updated
October 27, 2019
Sponsor
The Clatterbridge Cancer Centre NHS Foundation Trust
1. Study Identification
Unique Protocol Identification Number
NCT02125175
Brief Title
BIOPROP20: Biologically Optimised IMRT for Prostate Radiotherapy Hypofractionated Radiotherapy With Intra-prostatic Boosts to Tumour Nodules in Men With Intermediate and High Risk Prostate Cancer
Acronym
BIOPROP20
Official Title
BIOPROP20: Biologically Optimised IMRT for Prostate Radiotherapy Hypofractionated Radiotherapy With Intra-prostatic Boosts to Tumour Nodules in Men With Intermediate and High Risk Prostate Cancer
Study Type
Interventional
2. Study Status
Record Verification Date
May 2019
Overall Recruitment Status
Completed
Study Start Date
January 2014 (undefined)
Primary Completion Date
September 2018 (Actual)
Study Completion Date
September 2019 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
The Clatterbridge Cancer Centre NHS Foundation Trust
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
High dose radiotherapy is a very effective treatment for prostate cancer. However, there is an increased risk of side effects compared to lower dose radiotherapy. This study will investigate the use of dose painting radiotherapy. Dose painting radiotherapy administers a high dose of radiotherapy to areas of cancer inside the prostate and a lower (standard) dose to the rest of the prostate. This may improve control of the cancer without increasing the side effects. The radiotherapy is given in 20 doses, called fractions.
Detailed Description
For patients with prostate cancer which has not spread, the typical treatment is hormone therapy and radiotherapy.
It is possible to identify areas within the prostate which contain a significant amount of cancer with functional MRI or with 18F choline PET CT scans. These areas are called Dominant Intraprostastic Lesions 'DILs'. Targeted prostate biopsies help to confirm scan results. The radiotherapy dose to the DILs is increased, whilst the rest of the prostate is treated with the standard dose. This technique is called dose painting or 'boost' Intensity Modulated Radiotherapy Treatment (IMRT).
IMRT is given in 37 treatment doses called fractions, once a day for about 8 weeks. A hypofractionated schedule is the administration of the total radiotherapy treatment over a smaller number of fractions, at a higher dose per fraction. Recent evidence suggests that the idea of using a 'hypofractionated' treatment schedule is better and more convenient with a similar number of side effects as a regular schedule.
In the study, 50 patients with intermediate/high risk prostate cancer suitable and fit for radical radiotherapy will be recruited. The patients undergo a staging functional MRI scan, fiducial marker insertion (required for image guided radiotherapy) and hormone therapy as per standard of care treatment. The choline PET CT scan and targeted prostate biopsies are optional. They are useful if the MRI is difficult to interpret and will be offered to patients if they are felt to be appropriate by the clinician. After 2 months hormone therapy (standard protocol) patients have a CT /MRI planning scan and undergo IMRT with 20 treatments (fractions).The patient will then be followed up until 24 months after they started radiotherapy treatment.
The main aim is to assess the side effects related to the bladder and bowel at 18 weeks (acute toxicity) after starting hypofractionated IMRT.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Prostate Cancer
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
55 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Hypofractionated IMRT boost Radiotherapy
Arm Type
Experimental
Intervention Type
Radiation
Intervention Name(s)
Hypofractionated IMRT boost Radiotherapy
Primary Outcome Measure Information:
Title
Acute bladder and bowel toxicity (NCI CTCAE v 4.0 and RTOG) at 18 weeks after the commencement of radiotherapy treatment
Time Frame
18 weeks
Secondary Outcome Measure Information:
Title
The success rate of producing dose painted IMRT plans which fulfill the dose-volume constraints as specified for the prostate and for the normal tissues
Time Frame
3 years
Title
Late bladder and bowel toxicity (NCI CTCAE v4) at 2 years
Time Frame
2 Years
10. Eligibility
Sex
Male
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Histologically confirmed adenocarcinoma of the prostate
NCCN intermediate/high risk disease and estimated risk of lymph node involvement 15 - 40%*
MRI stage T2a-T4 N0M0
Age 18-80 years
Normal blood count (Hb >11g/dl, WBC > 4000/mm3, platelets >100,000/mm3)
WHO performance status 0 or 1
Fully informed written consent
Risk of pelvic lymph node involvement = (Gleason score - 6) x 10 + 2/3 PSA
Exclusion Criteria:
Prior radiotherapy to the prostate or pelvis
Prior hormone therapy or radical prostatectomy
Total hip replacement
Clinically significant inflammatory bowel disease
Contraindication to have diagnostic MRI scans
Unable to have a general anaesthetic
Anti-coagulant therapy which cannot be temporarily stopped
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Isabel Syndikus, MD
Organizational Affiliation
The Clatterbridge Cancer Centre NHS Foundation Trust
Official's Role
Principal Investigator
Facility Information:
Facility Name
The Clatterbridge Cancer Centre NHS Foundation Trust
City
Bebington
State/Province
Wirral
ZIP/Postal Code
CH63 4JY
Country
United Kingdom
12. IPD Sharing Statement
Citations:
PubMed Identifier
27692920
Citation
Onjukka E, Uzan J, Baker C, Howard L, Nahum A, Syndikus I. Twenty Fraction Prostate Radiotherapy with Intra-prostatic Boost: Results of a Pilot Study. Clin Oncol (R Coll Radiol). 2017 Jan;29(1):6-14. doi: 10.1016/j.clon.2016.09.009. Epub 2016 Sep 29.
Results Reference
derived
Learn more about this trial
BIOPROP20: Biologically Optimised IMRT for Prostate Radiotherapy Hypofractionated Radiotherapy With Intra-prostatic Boosts to Tumour Nodules in Men With Intermediate and High Risk Prostate Cancer
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