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Feasibility Study Into Adjustment of the Radiation Beam to Account for Prostate Motion During Radiotherapy. (CALYPSO)

Primary Purpose

Prostate Cancer

Status
Completed
Phase
Not Applicable
Locations
Australia
Study Type
Interventional
Intervention
Prostate cancer radiotherapy using real-time tracking
Sponsored by
Royal North Shore Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Prostate Cancer focused on measuring Prostate Cancer, Real-time tracking, Radiotherapy, Dynamic Multileaf Collimator

Eligibility Criteria

35 Years - 85 Years (Adult, Older Adult)MaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients undergoing external beam radiotherapy at Northern Sydney Cancer Centre
  • Histologically proven prostate adenocarcinoma
  • Prostate Specific Antigen (PSA) obtained within 3 months prior to enrolment.
  • Patient must be able to have Varian Calypso beacons placed in the prostate (if on anticoagulants, must be cleared by Local Medical Officer or cardiologist).
  • ECOG performance status 0-2
  • Ability to understand and the willingness to sign a written informed consent document.
  • Body habitus enabling Calypso tracking (as per Calypso Determining a Patient's Localisation Designation & Orientation before implantation)
  • Prostate dimension that allows leaf span with tracking margin of ±8mm

Exclusion Criteria:

  • Previous pelvic radiotherapy
  • Prior total prostatectomy
  • Pacemaker
  • Implantable defibrillator
  • Insulin infusion pump
  • Hip prosthesis
  • Unwilling or unable to give informed consent
  • Unwilling or unable to complete quality of life questionnaires.

Sites / Locations

  • Northern Sydney Cancer Centre, Royal North Shore Hospital

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Real-time tracking & beam adjustment

Arm Description

Prostate cancer radiotherapy using real-time tracking

Outcomes

Primary Outcome Measures

Percentage of fractions being successfully delivered with Calypso-guided tracking.
The primary endpoint of this Pilot study is to evaluate the feasibility of implementing realtime adaptive radiotherapy using DMLC. This will be assessed as greater than 95% of fractions being successfully delivered (no equipment failures and tracking MLC follows beacons) with Calypso-guided tracking.

Secondary Outcome Measures

Improvement in overall beam-target geometric alignment.
Geometric alignment will be measured as average difference between beacon centroid and shifted MLC against original MLC.
Improvement in dosimetric coverage of prostate and normal healthy structures.
Dosimetric improvement will be assessed by applying the methods of Poulsen to reconstruct delivered dose distributions for each fraction of patient cohort and summed total dose. Preliminary data demonstrates dose reconstruction to follow the planned dose distribution, potentially even for ultrahypofractionated cases with longer treatment duration and Flattening Filter Free (FFF) delivery with larger potential delivery error per time increment.
Acute toxicity
Portion of patients with grade 3 or greater genitourinary or gastrointestinal toxicity assessed using the Modified Radiation Therapy Oncology Group (RTOG) Toxicity Scale.
Late toxicity
Ongoing reporting of gastrointestinal and genitourinary toxicity of the DMLC tracking cohort will be compared to matched pair controls using the modified RTOG scale.
Biochemical control
Ongoing biochemical control of the DMLC tracking cohort will be compared to matched pair controls using Prostate Specific Antigen (PSA).

Full Information

First Posted
January 9, 2014
Last Updated
June 10, 2021
Sponsor
Royal North Shore Hospital
Collaborators
University of Sydney
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1. Study Identification

Unique Protocol Identification Number
NCT02033343
Brief Title
Feasibility Study Into Adjustment of the Radiation Beam to Account for Prostate Motion During Radiotherapy.
Acronym
CALYPSO
Official Title
Phase I Feasibility Study of Prostate Cancer Radiotherapy Using Realtime Dynamic Multileaf Collimator Adaptation and Radiofrequency Tracking (Calypso)
Study Type
Interventional

2. Study Status

Record Verification Date
June 2021
Overall Recruitment Status
Completed
Study Start Date
October 2013 (Actual)
Primary Completion Date
February 2018 (Actual)
Study Completion Date
February 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Royal North Shore Hospital
Collaborators
University of Sydney

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this study is to monitor movement of the prostate during radiotherapy and adjust the radiation beam to account for any motion seen. This will increase the radiation dose to the prostate and decrease the dose to the rectum and bladder.
Detailed Description
Prostate cancer now accounts for one third of all new cancer diagnoses in men and approximately 30% of men will have external beam radiotherapy as their primary local therapy. Prostate motion during radiotherapy can be divided into interfraction and intrafraction motion. Interfraction motion has been well established and has been largely overcome by daily online image verification with either ultrasound, online CT or implanted fiducial markers, however motion during the radiation beam on time (intrafraction motion) is not corrected and can be the cause of significant errors in radiation dose delivery. The most common technology utilised in 2012 to allow prostate gating is the Calypso system. The Calypso system consists of implantable electromagnetic transponders, an array that contains source and receiver coils, computers for data analysis and display purposes, and an infrared camera system to localise the electromagnetic array in the treatment room. The array is placed over the patient, and the source coil in the array emit an electromagnetic signal that excites the transponders. Once the transponders are excited, the source coils are turned off and the receiver coils detect the signal emitted from the excited transponders. This process is repeated at a rate of 10 Hz, providing a realtime radiofrequency localisation of the prostate triangulating three implanted beacons. The current study will investigate using the continuous prostate positioning data from Calypso to integrate with the treatment beam delivery and allow real-time adaptation based on the prostate motion. This is called Realtime Dynamic Multileaf Collimator (DMLC) tracking. In this technique the multileaf collimator motion is altered in the gantry head in real time during beam delivery to account for the measured prostate motion. The proposed study is examining the dosimetric impact of accounting for intrafraction motion with Calypso and DMLC tracking. We hypothesise the improvements in delivered prostate dose with DMLC tracking will be even greater than gating. This improved treatment delivery will ensure that the prostate cancer receives the appropriate dose and that normal tissues are spared from extra radiation.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Prostate Cancer
Keywords
Prostate Cancer, Real-time tracking, Radiotherapy, Dynamic Multileaf Collimator

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
30 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Real-time tracking & beam adjustment
Arm Type
Experimental
Arm Description
Prostate cancer radiotherapy using real-time tracking
Intervention Type
Radiation
Intervention Name(s)
Prostate cancer radiotherapy using real-time tracking
Intervention Description
Radiotherapy delivered using Calypso radiofrequency emitting beacon guided real-time prostate localisation and beam adjustment using Dynamic Multi-leaf Collimator tracking software.
Primary Outcome Measure Information:
Title
Percentage of fractions being successfully delivered with Calypso-guided tracking.
Description
The primary endpoint of this Pilot study is to evaluate the feasibility of implementing realtime adaptive radiotherapy using DMLC. This will be assessed as greater than 95% of fractions being successfully delivered (no equipment failures and tracking MLC follows beacons) with Calypso-guided tracking.
Time Frame
2 years
Secondary Outcome Measure Information:
Title
Improvement in overall beam-target geometric alignment.
Description
Geometric alignment will be measured as average difference between beacon centroid and shifted MLC against original MLC.
Time Frame
2 years
Title
Improvement in dosimetric coverage of prostate and normal healthy structures.
Description
Dosimetric improvement will be assessed by applying the methods of Poulsen to reconstruct delivered dose distributions for each fraction of patient cohort and summed total dose. Preliminary data demonstrates dose reconstruction to follow the planned dose distribution, potentially even for ultrahypofractionated cases with longer treatment duration and Flattening Filter Free (FFF) delivery with larger potential delivery error per time increment.
Time Frame
2 years
Title
Acute toxicity
Description
Portion of patients with grade 3 or greater genitourinary or gastrointestinal toxicity assessed using the Modified Radiation Therapy Oncology Group (RTOG) Toxicity Scale.
Time Frame
Assessed up to 12 weeks post treatment
Title
Late toxicity
Description
Ongoing reporting of gastrointestinal and genitourinary toxicity of the DMLC tracking cohort will be compared to matched pair controls using the modified RTOG scale.
Time Frame
Up to five years
Title
Biochemical control
Description
Ongoing biochemical control of the DMLC tracking cohort will be compared to matched pair controls using Prostate Specific Antigen (PSA).
Time Frame
Up to five years

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
35 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients undergoing external beam radiotherapy at Northern Sydney Cancer Centre Histologically proven prostate adenocarcinoma Prostate Specific Antigen (PSA) obtained within 3 months prior to enrolment. Patient must be able to have Varian Calypso beacons placed in the prostate (if on anticoagulants, must be cleared by Local Medical Officer or cardiologist). ECOG performance status 0-2 Ability to understand and the willingness to sign a written informed consent document. Body habitus enabling Calypso tracking (as per Calypso Determining a Patient's Localisation Designation & Orientation before implantation) Prostate dimension that allows leaf span with tracking margin of ±8mm Exclusion Criteria: Previous pelvic radiotherapy Prior total prostatectomy Pacemaker Implantable defibrillator Insulin infusion pump Hip prosthesis Unwilling or unable to give informed consent Unwilling or unable to complete quality of life questionnaires.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Thomas N Eade, MBBS
Organizational Affiliation
Royal North Shore Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Northern Sydney Cancer Centre, Royal North Shore Hospital
City
St Leonards
State/Province
New South Wales
ZIP/Postal Code
2065
Country
Australia

12. IPD Sharing Statement

Citations:
PubMed Identifier
26194684
Citation
Colvill E, Booth JT, O'Brien RT, Eade TN, Kneebone AB, Poulsen PR, Keall PJ. Multileaf Collimator Tracking Improves Dose Delivery for Prostate Cancer Radiation Therapy: Results of the First Clinical Trial. Int J Radiat Oncol Biol Phys. 2015 Aug 1;92(5):1141-1147. doi: 10.1016/j.ijrobp.2015.04.024. Epub 2015 Apr 17.
Results Reference
background
PubMed Identifier
24506591
Citation
Keall PJ, Colvill E, O'Brien R, Ng JA, Poulsen PR, Eade T, Kneebone A, Booth JT. The first clinical implementation of electromagnetic transponder-guided MLC tracking. Med Phys. 2014 Feb;41(2):020702. doi: 10.1118/1.4862509.
Results Reference
result
PubMed Identifier
25186380
Citation
Colvill E, Poulsen PR, Booth JT, O'Brien RT, Ng JA, Keall PJ. DMLC tracking and gating can improve dose coverage for prostate VMAT. Med Phys. 2014 Sep;41(9):091705. doi: 10.1118/1.4892605.
Results Reference
result

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Feasibility Study Into Adjustment of the Radiation Beam to Account for Prostate Motion During Radiotherapy.

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