Prostate Cancer
Conditions
Brief summary
A single arm phase II study of prostate motion for prostate cancer to primarily compare prostate motion between different treatment duration for IMRT and VMAT.
Detailed description
Primarily, this is a single arm phase I study of prostate motion for prostate cancer to primarily compare prostate motion between different treatment duration for IMRT and VMAT. The radiation therapy is to be delivered using intensity modulated radiotherapy (IMRT) or Volumetric Modulated Arc therapy (VMAT) with the aid of volumetric image guidance to ensure accuracy and real-time 3D ultrasound images as observational record of the prostate motion. All the recruited patients are prescribed and treated with either VMAT or IMRT treatment. In order to simulate the behaviour of prostate motion in an IMRT scenario, the group of VMAT patients will be required to remain in treatment position for an additional 7 minutes depending on techniques used (once a week). In order to assess the level of acceptance of the treatment position, responses to the same comfort survey for the current treatment position (i.e. using leg immobiliser) by a cohort of 60 patients treated in another IGRT treatment room will be used as the baseline. In addition, RTT satisfaction questionnaire will also be administered to assess the handling of the new immobilizer. Acute toxicity will be measured at preset intervals using CTCAE version 3.0 and as will International prostate symptom score (IPSS) questionnaire which focuses on urinary symptoms. Symptoms or toxicities reported from this study is relevant for patients treated with IMRT or VMAT with full bladder protocol.
Interventions
None listed
Sponsors
National Cancer Centre, Singapore
Study design
Observational model
CASE_ONLY
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
MALE
Age
21 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Patient must be able to provide study-specific informed consent prior to study entry.
Exclusion criteria
* Patient who cannot abide to the departmental hydration protocol * Prostatectomy cases * Acquired Immune Deficiency Syndrome (AIDS) based upon current CDC definition; note, however, that HIV testing is not required for entry into this protocol. The need to exclude patients with AIDS from this protocol is necessary because the treatment involved in this protocol requires contact of ultrasound probe to the perineum area. * Patient enrolled in other clinical trials
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The extent of intra-fraction prostate motion using an ultrasound system during IMRT and during RapidArc therapy | 2 years |
Secondary
| Measure | Time frame |
|---|---|
| The 3D ultrasound capability of the Clarity® system (from Elekta AB Stockholm, Sweden) in providing real-time information of the prostate movement during the treatment delivery | 2 years |
| The efficacy of full bladder protocol for patient undergoing prostate radiotherapy | 2 years |
| The rate of acute GI and GU side effects within 3 months (<90 days) after radical radiotherapy | 2 years |
| Patient comfort, compliance and tolerance of two setup techniques | 2 years |
Countries
Singapore
Outcome results
None listed